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2-{[2-(4-bromobenzoyl)-5-methyl]phenyl}benzoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1415419-70-3

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1415419-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415419-70-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,4,1 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1415419-70:
(9*1)+(8*4)+(7*1)+(6*5)+(5*4)+(4*1)+(3*9)+(2*7)+(1*0)=143
143 % 10 = 3
So 1415419-70-3 is a valid CAS Registry Number.

1415419-70-3Downstream Products

1415419-70-3Relevant academic research and scientific papers

Palladium-catalyzed ortho-acylation of 2-arylbenzoxazoles and 2-arylbenzothiazoles using arylmethyl alcohols as the acyl source

Zhang, Qian,Yang, Fan,Wu, Yangjie

supporting information, p. 4908 - 4914 (2013/06/26)

A facile and efficient way for the synthesis of the acylated 2-arylbenzoxazoles and 2-arylbenzothiazoles by heterocycle-directed ortho-acylation was developed. This reaction was performed in chlorobenzene, using arylmethyl alcohols and tert-butyl hydroperoxide (TBHP) as the easily accessible acyl source and the oxidant, respectively, affording the desired products in moderate to good yields.

Palladium-catalyzed ortho-acylation of 2-arylbenzoxazoles

Zhang, Qian,Li, Chao,Yang, Fan,Li, Jingya,Wu, Yangjie

supporting information, p. 320 - 326 (2013/01/15)

An efficient and facile catalytic protocol for benzoxazole-directed ortho-acylation of 2-arylbenzoxazoles has been described using aldehydes as the easily accessible acyl source. This catalytic system was performed in the presence of tert-butyl hydroperoxide (TBHP) as the oxidant in chlorobenzene, affording the acylated 2-arylbenzoxazoles in moderate to good yields. The acylation exhibited high regioselectivity for the substrates containing a meta-substituent in the benzene ring and typically occurred at the less sterically hindered ortho-C-H bond of the directing group.

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