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benzofuran-2-yl(2-bromophenyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

733768-86-0

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733768-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 733768-86-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,3,7,6 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 733768-86:
(8*7)+(7*3)+(6*3)+(5*7)+(4*6)+(3*8)+(2*8)+(1*6)=200
200 % 10 = 0
So 733768-86-0 is a valid CAS Registry Number.

733768-86-0Relevant academic research and scientific papers

Synthesis, characterization, and antimicrobial activity of new benzofuran derivatives

Kenchappa,Bodke, Yadav D.,Telkar, Sandeep,Sindhe, M. Aruna,Giridhar

, p. 2827 - 2836 (2017/03/22)

A novel series of (5-substituted-1-benzofuran-2-yl)(2,4-substituted phenyl)methanones (4a–4i) have been prepared by the Knoevenagel condensation of (5-substituted-1-benzofuran-2-yl)(2,4-substituted phenyl)methanone (3a–3i) with Meldrum’s acid. The structu

Intramolecular oxidative coupling: I2/TBHP/NaN3-mediated synthesis of benzofuran derivatives

Xu, Wengang,Li, Qingcui,Cao, Chuanpeng,Zhang, Fanglin,Zheng, Hua

supporting information, p. 6158 - 6161 (2015/06/08)

A novel intramolecular oxidative coupling reaction has been established to prepare benzofuran derivatives via direct C(sp2)-H functionalization for the formation of C-O bond. This transformation is mediated by I2/TBHP/NaN3 under metal-free conditions and a catalytic amount of NaN3 plays a crucial role in the reaction. Furthermore, the reaction tolerates a broad substrate scope with average to excellent yields.

Synthesis of benzo[b]naphtho[2,3-d]furan-6,11-dione via one-pot remote anionic fries rearrangement and metalation reaction

Azevedo, Mariangela S.,Alves, Glaucia B. C.,Cardoso, Jari N.,Lopes, Rosangela S. C.,Lopes, Claudio C.

, p. 1262 - 1268 (2007/10/03)

The use of a lithiation reaction to transform the bromo-arylcarbamate 8a into the corresponding benzo[b]naphtho[2,3-d]furan-6,11-dione (2) is described.

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