Category: 517-23-7

Payami, Elmira published the artcileA novel composite electrode material derived from bisferrocenyl-functionalized GO and PANI for high performance supercapacitor, HPLC of Formula: 517-23-7, the publication is Electrochimica Acta (2020), 136712, database is CAplus.

A novel bisferrocenyl based epoxy compound was synthesized to be used for further surface modification of graphene oxide (GO). GO surface was firstly modified with ethylenediamine (EDA) as an amine linker and then bisferrocenyl based epoxy compound was covalently grafted to the GO surface through the epoxide ring opening reaction. Afterwards, polyaniline (PANI) nanofibers were phys. adsorbed onto the surface of the modified GO to obtain a potentially high-performance nanocomposite for battery-type supercapacitor applications. The surface modification, crystalline structure, morphol., composition, and microstructure of the synthesized nanocomposites were further studied using FTIR spectroscopy (FTIR), XRD, field emission SEM (FESEM), energy dispersive X-ray (EDX) and N₂ adsorption/desorption analyses, resp. Also, the electrochem. behavior of the synthesized nanocomposites was studied by electrochem. methods of cyclic voltammetry (CV), electrochem. impedance spectroscopy (EIS), galvanostatic charge-discharge measurement (GCD). The final nanocomposite electrode exhibited a charge storage capacity of 272 mAh g^-1, and capacity retention of 89% over 3000 CV cycles. A high energy d. of 69.3 Wh kg^-1 and high power d. of 6171 W kg^-1 were achieved in a sym. two-electrode configuration.

Electrochimica Acta published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C6H8O3, HPLC of Formula: 517-23-7.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Rajalakshmi, K. published the artcileVibrational assignments of α-acetyl -γ- butyrolactone by ab initio Hartree-Fock and density functional methods, Application of 3-Acetyldihydrofuran-2(3H)-one, the publication is International Journal of ChemTech Research (2018), 11(6), 145-159, database is CAplus.

The Fourier transform IR and FT-Raman spectra of α-acetyl-γ-butyrolactone have been recorded in region 4,000-400 and 4,000-100 cm^-1 resp. A complete assignment and anal. of fundamental vibration modes of the mol. have been carried out. The observed fundamental modes have been compared with harmonic vibration frequencies computed using d. functional theory calculations by employing B3LYP functional at 6-311 + G(d,p) level. UV-Visible spectrum of the compound has been recorded and electronic properties, such as HOMO (HOMO) and LUMO (LUMO) energies have been calculated with B3LYP/6-311 + + G(d,p) level. These calculated energies show that charge transfer occurs within mol. Mulliken population anal. and thermodn. properties of title compound have also been calculated

International Journal of ChemTech Research published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C6H8O3, Application of 3-Acetyldihydrofuran-2(3H)-one.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Kozma, Viktoria published the artcileConjugate addition of 1,3-dicarbonyl compounds to maleimides using bifunctional primary amine-(thio)phosphoramide organocatalysts, COA of Formula: C6H8O3, the publication is Molecular Catalysis (2022), 112089, database is CAplus.

Asym. Michael additions of 1,3-dicarbonyl compounds to N-substituted maleimides were carried out using primary amine-(thio)phosphoramide bifunctional chiral organocatalysts derived from optically pure C2-sym. 1,2-diamines. The addition of Et 2-fluoroacetoacetate using the 1,2-diphenylethane-1,2-diamine derived thiophosphoramide catalyst afforded various succinimides substituted with fluorine bearing quaternary carbon in high yields, good diastereomeric ratios and excellent enantiomeric excesses. Alicyclic β-ketoesters provided the diastereomerically pure Michael adducts in good yields and high enantioselectivities, whereas 2,4-pentanedione afforded products with slightly lower enantiomeric excesses. The bulkiness of the N-substituent of the maleimide ring influenced mostly the conversions. The thiophosphoramide catalyst was found also efficient in the addition of Et 2-fluoroacetoacetate to β-nitrostyrenes. Unprecedentedly, during this work the highly enantioselective addition of 1,3-dicarbonyl compounds to maleimides were catalyzed by a primary amine-hydrogen-bond donor groups containing bifunctional organocatalyst. These reactions occurred through enamine intermediate, as evidenced by electrospray-ionization mass spectrometry and NMR spectroscopy.

Molecular Catalysis published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C6H8O3, COA of Formula: C6H8O3.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Yang, Ziyue published the artcileSelf-healing supramolecular waterborne polyurethane dispersions with quadruple hydrogen bonds in main chain, Related Products of esters-buliding-blocks, the publication is Journal of Applied Polymer Science (2020), 137(45), 49413, database is CAplus.

A facile method for preparing supramol. waterborne polyurethane (WPU) based on quadruple hydrogen bonds (4H-WPU) is reported. Herein, 4H-WPU with quadruple hydrogen bonds in main chain were synthesized by poly (1,4-butylene-neopentylene adipate glycol) as soft segment, 2-ureido-4[1H]-pyrimidinone (UPy) functionalized monomer, isophorone diisocyanate, 2,2-Bis(hydroxymethyl)propionic acid (hydrophilic monomer), isophoronediamine, triethylamine (neutralizer), and monoethanolamine (blocking agent) as hard segment. The mol. weight of 4H-WPU was controlled around 18,000 consistently. The properties of 4H-WPU with different content of hydrophilic group, hard segment, and UPy units were characterized and the results could provide the reference for preparing supramol. WPU with high mech. and self-healing performance while maintaining dispersion stability. The tensile strength of 4H-WPU was 10 times of the blank sample. The healing time of scratched 4H-WPU film was inversely proportional to the content of UPy-functionalized monomer and the shortest healing time is 2.5 h at 80°C. Mech. performance of healed films can be restored to more than 90%.

Journal of Applied Polymer Science published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C4H6O3, Related Products of esters-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Hayrapetyan, Davit published the artcileFacile Synthesis of Spirocyclic Lactams via [3+2] and [3+3] Aza-Annulation Reactions, COA of Formula: C6H8O3, the publication is European Journal of Organic Chemistry (2021), 2021(14), 2121-2125, database is CAplus.

Spirocyclic pyrrolidones and piperidones such as I and II were synthesized starting from readily available α-ketolactones and α-ketolactams employing [3+2]- and [3+3]-aza-annulation reactions. Tandem reactions of enamino lactams and lactones with maleic and itaconic anhydride yielded alkylidenespirolactams in good yields; further reduction of the exocyclic C=C double bond of the enamino moiety proceeded with excellent diastereoselectivity. Overall, one C-C and two C-N bonds, as well as three new stereocenters were created in a diastereoselective manner resulting in a fast upbuild of mol. complexity.

European Journal of Organic Chemistry published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C6H8O3, COA of Formula: C6H8O3.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Nugent, Jeremy published the artcileSynthesis of α-quaternary bicyclo[1.1.1]pentanes through synergistic organophotoredox and hydrogen atom transfer catalysis, Recommanded Product: 3-Acetyldihydrofuran-2(3H)-one, the publication is Organic Letters (2021), 23(21), 8628-8633, database is CAplus and MEDLINE.

Bicyclo[1.1.1]pentanes (BCPs) are of importance in drug design as sp3-rich bioisosteres of arenes and tert-Bu groups, however the preparation of BCPs with adjacent quaternary carbons is barely known. Authors report a facile synthesis of α-quaternary BCPs using organophotoredox and hydrogen atom transfer catalysis in which α-keto radicals, generated through oxidation of β-ketocarbonyls, underwent efficient addition to [1.1.1]propellane. The BCP products can be transformed into a variety of useful derivatives including enantioenriched BCPs featuring α-quaternary stereocenters.

Organic Letters published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C6H8O3, Recommanded Product: 3-Acetyldihydrofuran-2(3H)-one.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Kumari, Aruna published the artcileGC-MS analysis of the methanol fraction of Ailanthus excelsa Roxb. fruit, Application of 3-Acetyldihydrofuran-2(3H)-one, the publication is Asian Journal of Pharmaceutical and Clinical Research (2022), 15(6), 51-55, database is CAplus.

The objective of the study was to evaluate the phytochem. compounds present in the methanolic fruit extract of Ailanthus excelsa. Phytochem. screening was carried out using the GC-MS instrument following the standard protocol. GC-MS studies revealed the presence of 65 compounds in fruit extract of Ailanthus excelsa. Among them, highest peak area (37.67%) was obtained for Mome Inositol (Six hydroxyl group polysaccharide) (Retention time 14.873). This study identifies the presence of pharmacol. active compounds which can be constructive for the formulation of novel drugs.

Asian Journal of Pharmaceutical and Clinical Research published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C6H8O3, Application of 3-Acetyldihydrofuran-2(3H)-one.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Xie, Haopu published the artcileThermally healable polyurethane with tailored mechanical performance using dynamic crosslinking motifs, Recommanded Product: 3-Acetyldihydrofuran-2(3H)-one, the publication is New Journal of Chemistry (2020), 44(32), 13584-13590, database is CAplus.

Materials with self-healing abilities have gained tremendous attention in recent years but combing excellent mech. performance and splendid self-healing capacity into a single polymer material is still a great challenge. In this study, a self-healing polyurethane (SHP) material was prepared by constructing a dynamic crosslinked network via quadruple hydrogen bonds formed from 5-(2-hydroxyethyl)-6-methyl-2-aminouracil (UPy). The mech. properties of the materials could be conveniently tuned by adjusting the dynamic crosslinked d. The optimal sample, SHP-75, has excellent mech. performance, showing high tensile strength (27.02 MPa), excellent stretchability (1300%), and prominent toughness (111.37 MJ m^-3). Despite such great mech. properties, SHP-75 exhibited superior self-healing abilities and could fully obtain its initial mech. strength after repairing at 80°C for 24 h. A self-healing conductive electrode was further constructed to demonstrate its application prospects in the field of sensing.

New Journal of Chemistry published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C15H21BO2, Recommanded Product: 3-Acetyldihydrofuran-2(3H)-one.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Wang, Wenliang published the artcileCatalytic fast pyrolysis of cellulose for increasing contents of furans and aromatics in biofuel production, Name: 3-Acetyldihydrofuran-2(3H)-one, the publication is Journal of Analytical and Applied Pyrolysis (2018), 93-100, database is CAplus.

The catalytic fast pyrolysis of cellulose, cellobiose and glucose with the zeolite catalyst of NaY was carried out using thermogravimetric analyzer (TG) and pyrolysis-gas chromatog./mass spectrometry (Py-GC/MS). Results from TG showed that all samples presented significant mass loss at low temperature and exhibited high residual chars with NaY. The activation energies of cellulose, cellobiose and glucose were significantly decreased with NaY. PY-GC/MS showed that saccharides were significantly decreased or even completely eliminated and converted into furans, aromatics, phenols and light oxygenates with NaY. The contents of furans of cellulose, cellobiose and glucose with NaY were increased from 17.48%, 18.79% and 28.77% to 46.71%, 52.11% and 67.81%, resp. Pyrolysis of cellulose and cellobiose presented high selectivity of BTX (Benzene, Toluene, and Xylene). The furans are mainly formed on the surface of NaY by dehydration, fragmentation/retro-aldol condensation, decarbonylation, or decarboxylation. The pyrolysis intermediates of anhydro-oligosaccharides dominated the formation of aromatics and phenols during the catalytic fast pyrolysis of cellulose in the zeolite catalyst pores at the active sites.

Journal of Analytical and Applied Pyrolysis published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C13H15NO6S, Name: 3-Acetyldihydrofuran-2(3H)-one.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Zhang, Jinhong published the artcileStudy on the Staged and Direct Fast Pyrolysis Behavior of Waste Pine Sawdust Using High Heating Rate TG-FTIR and Py-GC/MS, Computed Properties of 517-23-7, the publication is ACS Omega (2022), 7(5), 4245-4256, database is CAplus and MEDLINE.

To understand the fast pyrolysis kinetics and product evolution of waste pine sawdust, high heating rate thermogravimetry-Fourier transform IR (TG-FTIR) was used to obtain the kinetic parameters and the chem. groups formed during the pyrolysis process, while pyrolysis-gas chromatog./mass spectrometry (Py-GC/MS) was used to investigate the detailed compositions of products under the staged (seven stages from 300 to 600°C) and direct fast pyrolysis process. Spectral bands were identified for acids, alcs., aldehydes, aromatics, esters, ethers, hydrocarbons, ketones, phenols, and sugars. Research found that the apparent activation energy for fast pyrolysis is much higher than that of slow pyrolysis. The evolution of CO₂ is the major deoxygenation route. Cracking mainly occurred at the 450°C stage with phenols, ketones, aldehydes, and sugars as the main products. The product distributions for different stages are significantly different; the selectivity of aldehydes decreased, while phenols showed an upward trend with an increase in pyrolysis temperature Ketones and sugars reached their peak values at 450°C. The changes in the mol. composition of each stage helped to understand the pyrolysis process. Compared with the staged pyrolysis, the direct pyrolysis process had higher selectivity of acids, aldehydes, esters, and sugars and lower selectivity of phenols, ketones, and alcs.

ACS Omega published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C11H8N2O2, Computed Properties of 517-23-7.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics