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3-acetyl-2-phenylbenzofuran is a chemical compound belonging to the benzofuran family, characterized by a benzene ring fused with a furan ring. It has a molecular formula of C15H10O2 and a molecular weight of 222.24 g/mol. The compound features a 3-acetyl group (a ketone group attached to the benzene ring) and a 2-phenyl group (a benzene ring attached to the benzofuran core). This organic molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of other organic compounds. Due to its complex structure and diverse functional groups, 3-acetyl-2-phenylbenzofuran exhibits unique chemical properties and reactivity, making it a subject of interest in organic chemistry research.

4265-21-8

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4265-21-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4265-21-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,6 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4265-21:
(6*4)+(5*2)+(4*6)+(3*5)+(2*2)+(1*1)=78
78 % 10 = 8
So 4265-21-8 is a valid CAS Registry Number.

4265-21-8Relevant academic research and scientific papers

Iminyl-radicals by electrochemical decarboxylation of α-imino-oxy acids: construction of indole-fused polycyclics

Wan, Jin-Lin,Cui, Jian-Feng,Zhong, Wei-Qiang,Huang, Jing-Mei

supporting information, p. 10242 - 10245 (2021/10/12)

Iminyl radicals are reactive intermediates that can be used for the construction of various valuable heterocycles. Herein, the electrochemical decarboxylation of α-imino-oxy acids for the generation of iminyl radicals has been accomplished under exogenous-oxidant- and metal-free conditions through the use ofnBu4NBr as a mediator. The resulting iminyl radicals undergo intramolecular cyclization smoothly with the adjacent (hetero)arenes to afford a series of indole-fused polycyclic compounds.

Nickel-Catalyzed Acyl Group Transfer of o-Alkynylphenol Esters Accompanied by C?O Bond Fission for Synthesis of Benzo[b]furan

Doi, Ryohei,Shimizu, Koji,Ikemoto, Yuma,Uchiyama, Masashi,Koshiba, Mikiko,Furukawa, Atsushi,Maenaka, Katsumi,Watanabe, Satoshi,Sato, Yoshihiro

, p. 2086 - 2092 (2021/02/27)

Herein, we report the nickel-catalyzed cascade C?O bond cleavage/cyclization of ortho-alkynylphenyl ester to construct a 3-acylbenzo[b]furan skeleton. As a result of reaction condition screening, the Ni(0)/IAd (1,3-Di(1-adamantyl)imidazole-2-ylidene) system was found to be optimal for catalytic conversion. Interestingly, the reaction exclusively gives 3-acylbenzo[b]furan instead of a decarbonylated product frequently observed in reactions mediated by acyl-nickel species. The catalyst loadings could be reduced to 5–10 mol %. We demonstrated the synthesis of a variety of functionalized 3-acylbenzofuran derivatives. We conducted stoichiometric study of nickel complexes as well as density functional theory (DFT) calculations to support a possible reaction mechanism.

Synthesis and biological evaluation of 3-functionalized 2-phenyl- and 2-alkylbenzo[b]furans as antiproliferative agents against human melanoma cell line

Kwiecień, Halina,Peru?yńska, Magdalena,Stachowicz, Karolina,Piotrowska, Katarzyna,Bujak, Joanna,Kopytko, Patrycja,Dro?dzik, Marek

, (2019/04/29)

The key function of microtubules and mitotic spindle in cell division make them attractive targets in anticancer therapy. In the present study, functionalized in 3 position 2-phenyl- and 2-alkylbenzo[b]furans were synthesized and evaluated as antitumor ag

Cycloaddition of arynes with lodonium ylides: A mild and general route for the synthesis of benzofuran derivatives

Huang, Xiao-Cheng,Liu, Yi-Lin,Liang, Yun,Pi, Shao-Feng,Wang, Feng,Li, Jin-Heng

supporting information; experimental part, p. 1525 - 1528 (2009/04/07)

A mild and general cycloaddition of arynes with iodonium ylides protocol has been developed for the synthesis of benzofurans. In the presence of CsF, ortho-silyl aryltriflates were reacted with iodonium ylides smoothly at room temperature in moderate to good yields.

CONDENSED FURAN DERIVATIVES AS ADENOSINE ANTAGONISTS

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Page 30-31, (2010/02/09)

A novel compound of the following formula (I): wherein Z is a phenyl or pyridyl which condenses to a furan ring; X is CH or N; R1 is hydrogen or optionally substituted lower alkyl; R2 is hydrogen, halogen or lower alkoxy; and R3

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