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4-chloro-2-(4-methylbenzoyl)benzothiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1268700-03-3

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1268700-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268700-03-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,7,0 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1268700-03:
(9*1)+(8*2)+(7*6)+(6*8)+(5*7)+(4*0)+(3*0)+(2*0)+(1*3)=153
153 % 10 = 3
So 1268700-03-3 is a valid CAS Registry Number.

1268700-03-3Downstream Products

1268700-03-3Relevant 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

Rucl33h2o catalyzed tandem reaction of alkynylbromides with 2-aminothiophenols in water: A convenient synthesis of 2-benzoylbenzothiazoles

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

experimental part, p. 1568 - 1573 (2012/01/14)

RuCl33H2O catalyzed tandem reaction of alkynyl bromides with 2-aminothiophenols mediated by water is shown to represent a convenient synthesis of 2-benzoylbenzothiazoles. In addition, the Ru(iii) catalyst could be readily recovered and efficiently reused together with water up to three times. CSIRO 2011.

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

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

experimental part, 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.

A novel and practical synthesis of 2-benzoylbenzothiazoles and 2-benzylbenzothiazoles

Fan, Xuesen,He, Yan,Wang, Yangyang,Xue, Zaikun,Zhang, Xinying,Wang, Jianji

experimental part, p. 899 - 902 (2011/03/18)

A novel methodology for the synthesis of 2-benzoylbenzothiazoles and 2-benzylbenzothiazoles through FeCl3·6H2O catalyzed, air oxidized tandem process from commercially available 2-aminothiophenols and phenylacetaldehydes by using an

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