Category: 870-50-8

Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. 870-50-8, formula is C10H18N2O4, Name is Di-tert-butyl diazene-1,2-dicarboxylate. They perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Quality Control of 870-50-8.

Kabes, Connor Q.;Maximuck, William J.;Ghosh, Subrata K.;Kumar, Anil;Bhuvanesh, Nattamai;Gladysz, John A. research published 《 Chiral Tricationic Tris(1,2-diphenylethylenediamine) Cobalt(III) Hydrogen Bond Donor Catalysts with Defined Carbon/Metal Configurations; Matched/Mismatched Effects upon Enantioselectivities with Enantiomeric Chiral Counter Anions》, the research content is summarized as follows. The enantiopure and diastereopure salts Λ- or Δ-[Co((S,S)-dpen)₃]³⁺ 2Cl^–BAr_f^– (Λ- or Δ-(S,S)-1³⁺ 2Cl^–BAr_f^–; dpen/BAr_f = 1,2-diphenylethylenediamine/B(3,5-C₆H₃(CF₃)₂)₄) and Λ-(S,S)-1³⁺ 3Cl^– are treated with salts of the enantiopure chiral monoanions (A^–) or dianions (A^2-) 3-bromocamphor-8-sulfonate (camphSO₃^–), 1,1′-binaphthyl-2,2′-diyl phosphate (and three 3,3′-disubstituted derivatives), a related biphenanthryl species, tartrate, and Sb₂(tart’)₂^2- (tart’ = [^–O₂C-CHO^–-CHO^–-CO₂^–]). The lipophilic salts Λ- or Δ-(S,S)-1³⁺ 2A^–BAr_f^–, Λ-(S,S)-1³⁺ A^2-BAr_f^–, and Λ-(S,S)-1³⁺ 3A^– are isolated as hydrates and characterized by NMR and microanalyses. In the presence of tertiary amines, many of these are highly enantioselective catalysts for additions of 1,3-dicarbonyl compounds to trans-β-nitrostyrene and di-tert-butylazodicarboxylate. The ee values for diastereomeric salts can exhibit significant differences (avg/high/median Δ_%ee = 10/63/6; matched/mismatched effect), and in a few cases, they are better than those obtained with Λ- or Δ-(S,S)-1³⁺ 2Cl^–BAr_f^–. The crystal structure of Δ-(S,S)-1³⁺ 2(1S)-camphSO₃^–BAr_f^– shows that the two sulfonate moieties H-bond to opposite (idealized) C₃-sym. faces of the trication, with a sep. O atom associated with each of the three syn-periplanar NH groups.

870-50-8, Di-tert-butyl azodicarboxylate, also known as Di-tert-butyl azodicarboxylate, is a useful research compound. Its molecular formula is C₁₀H₁₈N₂O₄ and its molecular weight is 230.26 g/mol. The purity is usually 95%.
Di-tert-butyl azodicarboxylate is a reagent used in the electrophilic amination of β-keto esters catalyzed by an axially chiral guanidine. Building block in an enantioselective synthesis of 3,6-dihyropyridazines employing organocatalysts such a L-proline or (S)-2-pyrrolidinyl tetrazole. Utilized in the asymmetric Friedel-Crafts amination via a chiral organocatalyst.
Di-tert-butyl azodicarboxylate is a reagent used in the preparation of acyl hydrazinedicarboxylates via photoorganocatalytic hydroacylation of dialkyl azodicarboxylates with aldehydes in presence of phenylglyoxylic acid as photocatalyst., Quality Control of 870-50-8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Glycerides are fatty acid esters of glycerol; they are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. 870-50-8, formula is C10H18N2O4, Name is Di-tert-butyl diazene-1,2-dicarboxylate. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Application In Synthesis of 870-50-8.

Kabes, Connor;Lucas, Reagan;Gunn, Jack;Gladysz, John research published 《 Chiral Cobalt(III) Tris(1,2-diamine) Catalysts That Incorporate Nitrogenous Base Containing Anions for the Bifunctional Activation of Nucleophiles and Electrophiles in Enantioselective Addition Reactions》, the research content is summarized as follows. Here, The lipophilic diastereomeric cobalt complexes Λ or Δ-[Co((S,S)-dpen)₃]³⁺ 2Cl-BArf- (Λ or Δ-(S,S)-2³⁺ 2Cl-BArf-; dpen/BArf- = 1,2-diphenylethylenediamine/B(3,5-C₆H₃(CF₃)₂)₄^–) ,salts of nicotinates, isonicotinates, related sulfonates, and N,N-dimethylaminobenzoate were applied addition reactions. The 6-chloronicotinate salt gaves slower rates and lower ee values, and the 6-aminonicotinate salt gave faster rates and higher ee values. The 6-Me, 2-methoxy, and unsubstituted analogs afforded intermediate results. The 6-aminonicotinate catalyst was applied to additions of di-Me malonate to aryl-substituted nitroolefins and additions of 1,3-dicarbonyl compounds to di-t-Bu azodicarboxylate, with average yields/ee values of 90%/85% and 94%/77%, resp. The authors were unaware of other ionic catalysts for which Bronsted bases was productively incorporated into the anions, which were seldom if ever purposefully functionalized in any manner.

Application In Synthesis of 870-50-8, Di-tert-butyl azodicarboxylate, also known as Di-tert-butyl azodicarboxylate, is a useful research compound. Its molecular formula is C₁₀H₁₈N₂O₄ and its molecular weight is 230.26 g/mol. The purity is usually 95%.
Di-tert-butyl azodicarboxylate is a reagent used in the electrophilic amination of β-keto esters catalyzed by an axially chiral guanidine. Building block in an enantioselective synthesis of 3,6-dihyropyridazines employing organocatalysts such a L-proline or (S)-2-pyrrolidinyl tetrazole. Utilized in the asymmetric Friedel-Crafts amination via a chiral organocatalyst.
Di-tert-butyl azodicarboxylate is a reagent used in the preparation of acyl hydrazinedicarboxylates via photoorganocatalytic hydroacylation of dialkyl azodicarboxylates with aldehydes in presence of phenylglyoxylic acid as photocatalyst., 870-50-8.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Polyesters are important plastics, with monomers linked by ester moieties. Phosphoesters form the backbone of DNA molecules. 870-50-8, formula is C10H18N2O4, Name is Di-tert-butyl diazene-1,2-dicarboxylate.Nitrate esters, such as nitroglycerin, are known for their explosive properties. Name: Di-tert-butyl diazene-1,2-dicarboxylate.

Jin, Yunhe;Zhang, Qingqing;Wang, Lifang;Wang, Xinyao;Meng, Changgong;Duan, Chunying research published 《 Convenient C(sp³)-H bond functionalisation of light alkanes and other compounds by iron photocatalysis》, the research content is summarized as follows. Herein, we report a practical iron-catalyzed photoredox system for C(sp³)-H transformation of light alkanes to C-N and C-C bonds under ambient temp was reported. The present method with abundant and inexpensive iron salts as photocatalysts exhibited high catalytic efficiency (turnover number up to 8000), mild conditions, and the convenience of being purified and scaled up without chromatog. A photo-induced ligand-to-metal charge transfer between Fe(III) and Cl- generated a highly active chlorine radical that sequentially acted as hydrogen atom transfer catalyst. Therefore, the sustainable, convenient, and environmentally friendly system will find wide applications in high-value-added transformation of natural alkanes with novel inspiration not only for organic synthesis, but also for designing catalytically active organic/inorganic materials.

Name: Di-tert-butyl diazene-1,2-dicarboxylate, Di-tert-butyl azodicarboxylate, also known as Di-tert-butyl azodicarboxylate, is a useful research compound. Its molecular formula is C₁₀H₁₈N₂O₄ and its molecular weight is 230.26 g/mol. The purity is usually 95%.
Di-tert-butyl azodicarboxylate is a reagent used in the electrophilic amination of β-keto esters catalyzed by an axially chiral guanidine. Building block in an enantioselective synthesis of 3,6-dihyropyridazines employing organocatalysts such a L-proline or (S)-2-pyrrolidinyl tetrazole. Utilized in the asymmetric Friedel-Crafts amination via a chiral organocatalyst.
Di-tert-butyl azodicarboxylate is a reagent used in the preparation of acyl hydrazinedicarboxylates via photoorganocatalytic hydroacylation of dialkyl azodicarboxylates with aldehydes in presence of phenylglyoxylic acid as photocatalyst., 870-50-8.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Glycerides are fatty acid esters of glycerol; they are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. 870-50-8, formula is C10H18N2O4, Name is Di-tert-butyl diazene-1,2-dicarboxylate. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Computed Properties of 870-50-8.

Ji, Guanfeng;Zhao, Liang;Wei, Jianwei;Cai, Junkai;He, Cheng;Du, Zenggang;Cai, Wei;Duan, Chunying research published 《 A Metal-Organic Framework as a Multiphoton Excitation Regulator for the Activation of Inert C(sp³)-H Bonds and Oxygen》, the research content is summarized as follows. The activation and oxidization of inert C(sp³)-H bonds into value-added chems. affords attractively economic and ecol. benefits as well as central challenge in modern chem. Inspired by the natural enzymic transformation, herein, we report a new multiphoton excitation approach to activate the inert C(sp³)-H bonds and oxygen by integrating the photoinduced electron transfer (PET), ligand-to-metal charge transfer (LMCT) and hydrogen atom transfer (HAT) events together into one metal-organic framework. The well-modified NAD (NAD⁺) mimics oxidized Ce^III-OEt moieties to generate Ce^IV-OEt chromophore and its reduced state mimics NAD^. via PET. The in situ formed Ce^IV-OEt moiety triggers a LMCT excitation to form the alkoxy radical EtO^., abstracts a hydrogen atom from the C(sp³)-H bond, accompanying the recovery of Ce^III-OEt and the formation of alkyl radicals. The formed NAD^. activates oxygen to regenerate the NAD⁺ for next recycle, wherein, the activated oxygen species interacts with the intermediates for the oxidization functionalization, paving a catalytic avenue for developing scalable and sustainable synthetic strategy.

Computed Properties of 870-50-8, Di-tert-butyl azodicarboxylate, also known as Di-tert-butyl azodicarboxylate, is a useful research compound. Its molecular formula is C₁₀H₁₈N₂O₄ and its molecular weight is 230.26 g/mol. The purity is usually 95%.
Di-tert-butyl azodicarboxylate is a reagent used in the electrophilic amination of β-keto esters catalyzed by an axially chiral guanidine. Building block in an enantioselective synthesis of 3,6-dihyropyridazines employing organocatalysts such a L-proline or (S)-2-pyrrolidinyl tetrazole. Utilized in the asymmetric Friedel-Crafts amination via a chiral organocatalyst.
Di-tert-butyl azodicarboxylate is a reagent used in the preparation of acyl hydrazinedicarboxylates via photoorganocatalytic hydroacylation of dialkyl azodicarboxylates with aldehydes in presence of phenylglyoxylic acid as photocatalyst., 870-50-8.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Ester is a chemical compound derived from an oxoacid (organic or inorganic) in which at least one –OH hydroxyl group is replaced by an –O– alkyl (alkoxy) group, 870-50-8, formula is C10H18N2O4, Name is Di-tert-butyl diazene-1,2-dicarboxylate. as in the substitution reaction of a carboxylic acid and an alcohol. Name: Di-tert-butyl diazene-1,2-dicarboxylate.

Jayakrishnan, K. R.;Tamilarasu, M.;Jincy, K. V.;Kaliyamoorthy, Alagiri research published 《 N-Heterocyclic carbene as a Bronsted base catalyst for the amination of naphthol derivatives and alcoholysis of glutaric anhydrides》, the research content is summarized as follows. A non-covalent Bronsted-basic N-heterocyclic carbene catalyzed (NHC) Friedel-Crafts type amination of naphthol derivatives using dialkyl azodicarboxylates as the aminating source was presented for the synthesis of aminonaphthols I [R = Et, i-Pr, t-Bu, Bn; R¹ = H, 3-Br, 6-Ph, etc.]. Also, alcoholysis of various glutaric anhydrides using alc. as pronucleophile was reported for the synthesis of dicarboxylic acid monoesters CO₂HCH(R²)CH(R⁴)(CH₂)_nCO₂R³ [R² = H, Ph; R³ = Me, Et, allyl, etc.; R⁴ = H, Ph, 4-FC₆H₄; n = 0,1]. Both of these reactions were performed in the presence of either com. available free-carbene catalyst or in situ-generated carbene catalyst. Both reactions proceed via in situ activations of -OH group by the carbene catalyst through hydrogen bonding interaction and furnished the relevant products in moderate to excellent yields.

870-50-8, Di-tert-butyl azodicarboxylate, also known as Di-tert-butyl azodicarboxylate, is a useful research compound. Its molecular formula is C₁₀H₁₈N₂O₄ and its molecular weight is 230.26 g/mol. The purity is usually 95%.
Di-tert-butyl azodicarboxylate is a reagent used in the electrophilic amination of β-keto esters catalyzed by an axially chiral guanidine. Building block in an enantioselective synthesis of 3,6-dihyropyridazines employing organocatalysts such a L-proline or (S)-2-pyrrolidinyl tetrazole. Utilized in the asymmetric Friedel-Crafts amination via a chiral organocatalyst.
Di-tert-butyl azodicarboxylate is a reagent used in the preparation of acyl hydrazinedicarboxylates via photoorganocatalytic hydroacylation of dialkyl azodicarboxylates with aldehydes in presence of phenylglyoxylic acid as photocatalyst., Name: Di-tert-butyl diazene-1,2-dicarboxylate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. 870-50-8, formula is C10H18N2O4, Name is Di-tert-butyl diazene-1,2-dicarboxylate. They perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Synthetic Route of 870-50-8.

Jalali, Mona;Ho, Curtis C.;Fuller, Rebecca O.;Lucas, Nigel T.;Ariafard, Alireza;Bissember, Alex C. research published 《 Photochemical Activation of a Hydroxyquinone-Derived Phenyliodonium Ylide by Visible Light: Synthetic and Mechanistic Investigations》, the research content is summarized as follows. We have identified and extensively investigated the photochem. activation and reaction of a hydroxyquinone-derived phenyliodonium ylide in the presence of visible light using experiment and theory. These studies revealed that in its photoexcited state this iodonium is capable of facilitating a range of single-electron transfer (SET) processes, including hydrogen atom transfer (HAT), a Povarov-type reaction, and atom-transfer radical addition chem. Where possible, we have employed d. functional theory (DFT) to develop a more complete understanding of these photoinduced synthetic transformations.

870-50-8, Di-tert-butyl azodicarboxylate, also known as Di-tert-butyl azodicarboxylate, is a useful research compound. Its molecular formula is C₁₀H₁₈N₂O₄ and its molecular weight is 230.26 g/mol. The purity is usually 95%.
Di-tert-butyl azodicarboxylate is a reagent used in the electrophilic amination of β-keto esters catalyzed by an axially chiral guanidine. Building block in an enantioselective synthesis of 3,6-dihyropyridazines employing organocatalysts such a L-proline or (S)-2-pyrrolidinyl tetrazole. Utilized in the asymmetric Friedel-Crafts amination via a chiral organocatalyst.
Di-tert-butyl azodicarboxylate is a reagent used in the preparation of acyl hydrazinedicarboxylates via photoorganocatalytic hydroacylation of dialkyl azodicarboxylates with aldehydes in presence of phenylglyoxylic acid as photocatalyst., Synthetic Route of 870-50-8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Ester is a chemical compound derived from an oxoacid (organic or inorganic) in which at least one –OH hydroxyl group is replaced by an –O– alkyl (alkoxy) group, 870-50-8, formula is C10H18N2O4, Name is Di-tert-butyl diazene-1,2-dicarboxylate. as in the substitution reaction of a carboxylic acid and an alcohol. Name: Di-tert-butyl diazene-1,2-dicarboxylate.

Jalaja, Renjitha;Leela, Shyni G.;Mohan, Sangeetha;Nair, Mangalam S.;Gopalan, Raghu K.;Somappa, Sasidhar B. research published 《 Anti-hyperlipidemic potential of natural product based labdane-pyrroles via inhibition of cholesterol and triglycerides synthesis》, the research content is summarized as follows. Hyperlipidemia is the clin. condition where blood has an increased level of lipids, such as cholesterol and triglycerides. Therefore controlling hyperlipidemia is considered to be a protective strategy to treat many associated diseases. Thus, a novel natural product-derived pyrrole and pyrazole (E)-labda-8(17),12-diene-15,16-dial conjugates possessing inhibition potential for cholesterol and triglyceride synthesis were designed through scaffold hopping approach and synthesized via one-pot selective cycloaddition Amongst the tested hybrids, 3i (I) exhibited excellent activity against triglyceride and cholesterol synthesis with the percentage inhibition of 71.73 ± 0.78 and 68.61 ± 1.19, which is comparable to the pos. controls fenofibrate and atorvastatin, resp. Compounds 3j and 3k (II and III, resp.) also exhibited the considerable potential of promising leads. The HMG CoA reductase inhibitory activity of the compounds was consistent with that of inhibitory activity of cholesterol synthesis. Compound 3i showed the highest inhibitory potential (78.61 ± 2.80) percentage of suppression, which was comparable to that of the pos. control pravastatin (78.05 ± 5.4). Favorably, none of the compounds showed cytotoxicity (HepG2) in the concentration ranging from 0.5 to 100μM.

870-50-8, Di-tert-butyl azodicarboxylate, also known as Di-tert-butyl azodicarboxylate, is a useful research compound. Its molecular formula is C₁₀H₁₈N₂O₄ and its molecular weight is 230.26 g/mol. The purity is usually 95%.
Di-tert-butyl azodicarboxylate is a reagent used in the electrophilic amination of β-keto esters catalyzed by an axially chiral guanidine. Building block in an enantioselective synthesis of 3,6-dihyropyridazines employing organocatalysts such a L-proline or (S)-2-pyrrolidinyl tetrazole. Utilized in the asymmetric Friedel-Crafts amination via a chiral organocatalyst.
Di-tert-butyl azodicarboxylate is a reagent used in the preparation of acyl hydrazinedicarboxylates via photoorganocatalytic hydroacylation of dialkyl azodicarboxylates with aldehydes in presence of phenylglyoxylic acid as photocatalyst., Name: Di-tert-butyl diazene-1,2-dicarboxylate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Ester is a chemical compound derived from an oxoacid (organic or inorganic) in which at least one –OH hydroxyl group is replaced by an –O– alkyl (alkoxy) group, 870-50-8, formula is C10H18N2O4, Name is Di-tert-butyl diazene-1,2-dicarboxylate. as in the substitution reaction of a carboxylic acid and an alcohol. Category: esters-buliding-blocks.

Hwang, Seunghae;Kim, Hyun-seung;Ryu, Ji Heon;Oh, Seung M. research published 《 N-(α-ferrocenyl)ethylphthalimide as single redox couple for non-aqueous flow batteries》, the research content is summarized as follows. To establish highly soluble single redox couple for non-aqueous flow batteries, N-(α-ferrocenyl)ethylphthalimide (α-FcEtPI) is derived from a promising single redox couple, N-ferrocenylphthalimide (FcPI), by inserting an α-Me group between the ferrocenyl and phthalimide moieties. The resulting material (α-FcEtPI) shows the maximum solubility of 0.81 M in 1.0 M tetrabutylammonium tetrafluoroborate (TBABF₄) in 1,3-dioxolane at 25 °C. This notable increase in solubility (vs. 0.3 M for FcPI) is attributed to the disruptive effect of the α-Me group on mol. packing in a solid state. α-FcEtPI exhibits two stable redox reactions at E_1/2 = 0.01 V and -1.97 V (vs. Fc/Fc⁺), thus functioning as a single redox couple with working voltage (E_wk) of 1.98 V. Considering the solubility and working voltage, the theor. energy d. of α-FcEtPI is calculated as 21.06 W h L^-1 (vs. 7.8 W h L^-1 for FcPI). The cell data of 0.6 M α-FcEtPI in 1 M TBABF₄ in 1,3-dioxolane electrolytes, indicates remarkably high Coulombic efficiency (97.8%) and excellent cycle retention.

870-50-8, Di-tert-butyl azodicarboxylate, also known as Di-tert-butyl azodicarboxylate, is a useful research compound. Its molecular formula is C₁₀H₁₈N₂O₄ and its molecular weight is 230.26 g/mol. The purity is usually 95%.
Di-tert-butyl azodicarboxylate is a reagent used in the electrophilic amination of β-keto esters catalyzed by an axially chiral guanidine. Building block in an enantioselective synthesis of 3,6-dihyropyridazines employing organocatalysts such a L-proline or (S)-2-pyrrolidinyl tetrazole. Utilized in the asymmetric Friedel-Crafts amination via a chiral organocatalyst.
Di-tert-butyl azodicarboxylate is a reagent used in the preparation of acyl hydrazinedicarboxylates via photoorganocatalytic hydroacylation of dialkyl azodicarboxylates with aldehydes in presence of phenylglyoxylic acid as photocatalyst., Category: esters-buliding-blocks

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Glycerides are fatty acid esters of glycerol; they are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. 870-50-8, formula is C10H18N2O4, Name is Di-tert-butyl diazene-1,2-dicarboxylate. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Product Details of C10H18N2O4.

Huang, Wenlin;Hulverson, Matthew A.;Choi, Ryan;Arnold, Samuel L. M.;Zhang, Zhongsheng;McCloskey, Molly C.;Whitman, Grant R.;Hackman, Robert C.;Rivas, Kasey L.;Barrett, Lynn K.;Ojo, Kayode K.;Van Voorhis, Wesley C.;Fan, Erkang research published 《 Development of 5-Aminopyrazole-4-carboxamide-based Bumped-Kinase Inhibitors for Cryptosporidiosis Therapy》, the research content is summarized as follows. Cryptosporidium is a leading cause of pediatric diarrhea worldwide. Currently, there is neither a vaccine nor a consistently effective drug available for this disease. Selective 5-aminopyrazole-4-carboxamide-based bumped-kinase inhibitors (BKIs) are effective in both in vitro and in vivo models of Cryptosporidium parvum. Potential cardiotoxicity in some BKIs led to the continued exploration of the 5-aminopyrazole-4-carboxamide scaffold to find safe and effective drug candidates for Cryptosporidium. A series of newly designed BKIs were tested for efficacy against C. parvum using in vitro and in vivo (mouse infection model) assays and safety issues. Compound 6 (BKI 1708) was found to be efficacious at 8 mg/kg dosed once daily (QD) for 5 days with no observable signs of toxicity up to 200 mg/kg dosed QD for 7 days. Compound 15 (BKI 1770) was found to be efficacious at 30 mg/kg dosed twice daily (BID) for 5 days with no observable signs of toxicity up to 300 mg/kg dosed QD for 7 days. Compounds 6 and 15 are promising preclin. leads for cryptosporidiosis therapy with acceptable safety parameters and efficacy in the mouse model of cryptosporidiosis.

Product Details of C10H18N2O4, Di-tert-butyl azodicarboxylate, also known as Di-tert-butyl azodicarboxylate, is a useful research compound. Its molecular formula is C₁₀H₁₈N₂O₄ and its molecular weight is 230.26 g/mol. The purity is usually 95%.
Di-tert-butyl azodicarboxylate is a reagent used in the electrophilic amination of β-keto esters catalyzed by an axially chiral guanidine. Building block in an enantioselective synthesis of 3,6-dihyropyridazines employing organocatalysts such a L-proline or (S)-2-pyrrolidinyl tetrazole. Utilized in the asymmetric Friedel-Crafts amination via a chiral organocatalyst.
Di-tert-butyl azodicarboxylate is a reagent used in the preparation of acyl hydrazinedicarboxylates via photoorganocatalytic hydroacylation of dialkyl azodicarboxylates with aldehydes in presence of phenylglyoxylic acid as photocatalyst., 870-50-8.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Polyesters are important plastics, with monomers linked by ester moieties. Phosphoesters form the backbone of DNA molecules. 870-50-8, formula is C10H18N2O4, Name is Di-tert-butyl diazene-1,2-dicarboxylate.Nitrate esters, such as nitroglycerin, are known for their explosive properties. HPLC of Formula: 870-50-8.

Hu, Zhiyun;Ge, Hongyu;Yang, Xinzheng research published 《 Binuclear O₂ activation and hydrogen transfer mechanism for aerobic oxidation of alcohols》, the research content is summarized as follows. A d. functional theory study of the aerobic oxidation of 1-phenylethanol into acetophenone catalyzed by phenanthroline copper (phenCu) complexes reveals a binuclear O₂ activation and hydrogen transfer mechanism with multiple spin-crossover steps. When di-tert-Bu azodicarboxylate (DBAD) exists, it acts as a stoichiometric oxidant and forms DBADH₂ through successive transfers of the proton and hydride from 1-phenylethanol to DBAD in one transition state with a free energy barrier of 21.8 kcal mol^-1. After the consumption of DBAD, DBADH₂ acts as a co-catalyst assisting O₂ activation and acetophenone formation through binuclear transition states for the cleavages of O-O and C-H bonds with a total free energy barrier of 24.6 kcal mol^-1. Without the presence of DBAD or DBADH₂, the total free energy barrier for the aerobic oxidation of 1-phenylethanol with the participation of two phenCu complexes is 26.1 kcal mol^-1. In all the above three situations, the rate-determining step is the activation of the C-H bond in 1-phenylethanol. The formation of HOO radical and the breaking of the O-O bond in hydrogen peroxide for the formation of a Cu(II)-hydroxyl dimer are also key steps in the reaction and need the participation of two phenCu complexes.

HPLC of Formula: 870-50-8, Di-tert-butyl azodicarboxylate, also known as Di-tert-butyl azodicarboxylate, is a useful research compound. Its molecular formula is C₁₀H₁₈N₂O₄ and its molecular weight is 230.26 g/mol. The purity is usually 95%.
Di-tert-butyl azodicarboxylate is a reagent used in the electrophilic amination of β-keto esters catalyzed by an axially chiral guanidine. Building block in an enantioselective synthesis of 3,6-dihyropyridazines employing organocatalysts such a L-proline or (S)-2-pyrrolidinyl tetrazole. Utilized in the asymmetric Friedel-Crafts amination via a chiral organocatalyst.
Di-tert-butyl azodicarboxylate is a reagent used in the preparation of acyl hydrazinedicarboxylates via photoorganocatalytic hydroacylation of dialkyl azodicarboxylates with aldehydes in presence of phenylglyoxylic acid as photocatalyst., 870-50-8.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics