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2-(4-bromobenzoyl)-5-chlorobenzoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1327274-40-7

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1327274-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1327274-40-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,7,2,7 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1327274-40:
(9*1)+(8*3)+(7*2)+(6*7)+(5*2)+(4*7)+(3*4)+(2*4)+(1*0)=147
147 % 10 = 7
So 1327274-40-7 is a valid CAS Registry Number.

1327274-40-7Downstream Products

1327274-40-7Relevant academic research and scientific papers

A sustainable synthesis of 2-benzoxazyl and 2-benzothiazyl ketones from alkynyl bromides and 2-amino(thio)phenols promoted by a recyclable catalytic system

Cui, Liangyan,He, Yan,Fan, Xuesen

experimental part, p. 992 - 996 (2012/05/20)

An environmentally and economically sustainable synthesis of 2-benzoxazyl ketones and 2-benzothiazyl ketones through FeCl3·6H 2O catalyzed tandem reactions of alkynyl bromides with 2-amino(thio)phenols in [bmim]BF4 has been developed. Remarkable advantages of this new synthetic strategy include high efficiency, readily available starting materials, and recyclable catalyst and reaction medium. An environmentally and economically sustainable synthesis of 2-benzoxazyl ketones and 2-benzothiazyl ketones through FeCl3·6H2O catalyzed tandem reactions of alkynyl bromides with 2-amino(thio)phenols in [bmim]BF4 has been developed. Remarkable advantages of this new synthetic strategy include high efficiency, readily available starting materials, and recyclable catalyst and reaction medium. Copyright

Synthesis of heteroaryl ketones via tandem reaction of 1,1-dibromoethenes

Fan, Xuesen,He, Yan,Zhang, Xinying,Guo, Shenghai,Wang, Yangyang

, p. 6369 - 6374 (2011/09/12)

A novel method for the synthesis of heteroaryl ketones through one-pot tandem reaction of 1,1-dibromoethenes with 2-amino(thio)phenols promoted by TBAF·3H2O and RuCl3(5%)/air was developed. This novel method includes several reactions in one-pot and utilizes economical yet efficient reagents to generate synthetically and biologically interesting heteroaryl ketones under mild conditions with good efficiency.

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