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3-Ethyl-3-phenylbenzofuran-2(3H)-one is a complex organic compound with the molecular formula C18H14O2. It is a derivative of benzofuran, which is a heterocyclic aromatic compound consisting of a benzene ring fused to a furan ring. The molecule features an ethyl group (-CH2CH3) and a phenyl group (C6H5) attached to the benzofuran core, with the carbonyl group (C=O) at the 2-position. 3-ethyl-3-phenylbenzofuran-2(3H)-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in organic chemistry. Due to its unique structure, it may exhibit specific chemical properties and reactivity, making it a subject of interest in research and development.

4374-69-0

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4374-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4374-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4374-69:
(6*4)+(5*3)+(4*7)+(3*4)+(2*6)+(1*9)=100
100 % 10 = 0
So 4374-69-0 is a valid CAS Registry Number.

4374-69-0Downstream Products

4374-69-0Relevant articles and documents

Palladium-catalyzed bisarylation of 3-alkylbenzofurans to 3-arylalkyl-2-arylbenzofurans on water: Tandem C(sp3)-H and C(sp2)-H activation reactions of 3-alkylbenzofurans

Cho, Beom Shin,Chung, Young Keun

, p. 14543 - 14546 (2015)

A protocol involving facile sequential C(sp3)-H and C(sp2)-H activation reactions of 3-alkylbenzofurans catalyzed by Pd(OAc)2 in the presence of pivalic acid, silver salt, and tricyclohexylphosphine 'on water' was developed. Aryl iodides were used as substrates in a tandem bisarylation reaction to generate 3-arylalkyl-2-arylbenzofurans in moderate to high yields at room temperature. The reaction revealed in this study is a rare example of consecutive C(sp3)-H and C(sp2)-H bond activation under mild reaction conditions.

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