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. Application of C10H18N2O4.
Varlet, Thomas;Levitre, Guillaume;Retailleau, Pascal;Masson, Geraldine research published 《 Catalyst-free cycloaddition of 1,3-diene-1-carbamates with azodicarboxylates: A rapid click reaction》, the research content is summarized as follows. A novel practical, catalyst-free, azo-Diels-Alder reaction between dienecarbamates RO(O)CNHCH=C(R1)C(R2)=CHR3 (R = benzyloxy, tert-butyloxy, (prop-2-en-1-yloxy); R1 = H, Me; R2 = H, Me; R3 = H, Me, i-Pr, Ph, (2S)-2,6-dimethylhept-5-en-1-yl) and azodicarboxylates e.g., dibenzyl azodicarboxylate exhibiting a remarkable functional group tolerance was reported. The availability of starting materials, mild reaction conditions, chemoselectivity and scalability make this cycloaddition a viable supplement to the other reactions in ”click” chem.
Application 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