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2-(4-fluorobenzoyl)-5-methylbenzofuran-3-ol is a complex organic chemical compound with the molecular formula C16H11FO3. It features a benzofuran core, which is a fused ring structure consisting of a benzene ring and a furan ring. The molecule is characterized by a 4-fluorobenzoyl group attached to the 2-position of the benzofuran, and a methyl group at the 5-position. Additionally, it has a hydroxyl group at the 3-position, which contributes to its reactivity and potential applications. 2-(4-fluorobenzoyl)-5-methylbenzofuran-3-ol may be of interest in the fields of pharmaceuticals, materials science, or as a synthetic intermediate due to its unique structure and functional groups.

4245-66-3

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4245-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4245-66-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,4 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4245-66:
(6*4)+(5*2)+(4*4)+(3*5)+(2*6)+(1*6)=83
83 % 10 = 3
So 4245-66-3 is a valid CAS Registry Number.

4245-66-3Downstream Products

4245-66-3Relevant 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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