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(benzotriazol-1-yl)(3-methyl-2-hydroxyphenyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

888487-61-4

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888487-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 888487-61-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,8,4,8 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 888487-61:
(8*8)+(7*8)+(6*8)+(5*4)+(4*8)+(3*7)+(2*6)+(1*1)=254
254 % 10 = 4
So 888487-61-4 is a valid CAS Registry Number.

888487-61-4Relevant academic research and scientific papers

Synthesis of aliphatic hydroxyaryl ketones or (hetero)aryl hydroxyaryl ketones by acylation of organometallic reagents

Katritzky, Alan R.,Le, Khanh N. B.,Mohapatra, Prabhu P.

, p. 3141 - 3146 (2007)

Diverse hydroxyarenecarboxylic acids afford stable N-(hydroxyaroyl) benzotriazoles that react with heteroaryl, alkyl, and aryl Grignard or lithium reagents to give the corresponding hydroxyaryl ketones in 51-94% yields. Georg Thieme Verlag Stuttgart.

Direct synthesis of esters and amides from unprotected hydroxyaromatic and -aliphatic carboxylic acids

Katritzky, Alan R.,Singh, Sanjay K.,Cai, Chunming,Bobrov, Sergey

, p. 3364 - 3374 (2007/10/03)

A facile method for the activation of hydroxy-substituted carboxylic acids using benzotriazole chemistry without prior protection of the hydroxy substituents is presented. The N-acylbenzotriazole intermediates 2a-g, 6a-d, and 9a-c have been used for high-yielding synthesis of both aliphatic (3a-1) and aromatic (7a-h, 10a-f) hydroxy carboxamides. High yields of aromatic hydroxy esters 12a-h and 13a-i were obtained using either neat alcohols in neutral microwave conditions or nucleophilic alkoxides and the intermediate N-(arylacyl)benzotriazoles. Moderate yields were obtained in the case of aliphatic hydroxy esters 11a,b and thiolesters 11e-g from the intermediates 2a-c.

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