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2-Benzoyl-5-methylbenzofuran-3-ol is a complex organic compound belonging to the class of benzofurans, characterized by a benzene ring fused to a furan ring. This specific compound features a methyl group at the 5-position and a benzoyl group (a benzene ring with a carbonyl group) attached to the 2-position of the benzofuran core. The 3-ol suffix indicates the presence of a hydroxyl (-OH) group at the 3-position. This molecule is known for its potential applications in pharmaceuticals and as a synthetic intermediate in the preparation of various biologically active compounds. Its chemical structure and properties make it a subject of interest in organic chemistry and medicinal chemistry research.

4010-51-9

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4010-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4010-51-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,1 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4010-51:
(6*4)+(5*0)+(4*1)+(3*0)+(2*5)+(1*1)=39
39 % 10 = 9
So 4010-51-9 is a valid CAS Registry Number.

4010-51-9Downstream Products

4010-51-9Relevant academic research and scientific papers

Efficient room-temperature synthesis and antimicrobial study of novel 2-aroylbenzofuran-3-ols from substituted methyl salicylates and phenacyl bromides

Kulkarni, Rashmi S.,Hanumanthappa, Suresha Kumara T.,Gopalpur, Nagendrappa,Vijaya Kumar, Sowmya H. B.,More, Sunil S.

supporting information, p. 331 - 339 (2014/01/06)

The article describes a convenient and efficient synthetic route for the construction of 2-aroylbenzofuran-3-ols from readily available diverse methyl salicylates and phenacyl bromides using K2CO3 as catalyst in dimethylformamide as solvent at room temperature. The reaction involves two steps, which occur in quick succession within 1 h to deliver the product with reasonably high yields. All the synthesized 2-aroylbenzofuran-3-ols (4a-u) were subjected for their antimicrobial studies, and some of these have shown prominent activity. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications for the following free supplemental resource(s): Full experimental and spectral details.]

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