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benzofuran-2-yl-(4-tert-butyl-phenyl)-methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14178-69-9

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14178-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14178-69-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,7 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14178-69:
(7*1)+(6*4)+(5*1)+(4*7)+(3*8)+(2*6)+(1*9)=109
109 % 10 = 9
So 14178-69-9 is a valid CAS Registry Number.

14178-69-9Relevant academic research and scientific papers

Tandem addition/cyclization for synthesis of 2-aroyl benzofurans and 2-aroyl indoles by carbopalladation of nitriles

Gong, Julin,Hu, Kun,Shao, Yinlin,Li, Renhao,Zhang, Yetong,Hu, Maolin,Chen, Jiuxi

, p. 488 - 494 (2020/02/03)

The first example of the palladium-catalyzed tandem addition/cyclization of 2-(2-acylphenoxy)acetonitriles with arylboronic acids has been developed, providing a new strategy for the synthesis of 2-aroyl benzofurans with excellent chemoselectivity and wid

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

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

, 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 and CYP26A1 inhibitory activity of 1-[benzofuran-2-yl-(4-alkyl/aryl-phenyl)-methyl]-1H-triazoles

Pautus, Stephane,Yee, Sook Wah,Jayne, Martyn,Coogan, Michael P.,Simons, Claire

, p. 3643 - 3653 (2007/10/03)

Methodology previously described by our group was applied to the preparation of a series of 4-alkyl/aryl-substituted 1-[benzofuran-2-yl-phenylmethyl]-1H-triazoles. The [1,2,4]-triazole derivatives were prepared for a range of alkyl and aryl substituents,

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