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3-Nitrobenzoic acid phenacyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55153-32-7

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55153-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55153-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,5 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55153-32:
(7*5)+(6*5)+(5*1)+(4*5)+(3*3)+(2*3)+(1*2)=107
107 % 10 = 7
So 55153-32-7 is a valid CAS Registry Number.

55153-32-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name phenacyl 3-nitrobenzoate

1.2 Other means of identification

Product number -
Other names 3-nitro-benzoic acid phenacyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:55153-32-7 SDS

55153-32-7Relevant academic research and scientific papers

Effect of binary aqueous-organic solvents on the reaction of phenacyl bromide with nitrobenzoic acid(s) in the presence of triethylamine

Nallu,Subramanian,Vembu,Hussain, A. Akber

, p. 401 - 409 (2004)

Second-order rate constants (k2) of the reaction between phenacyl bromide and equimolar mixture of nitrobenzoic acid(s)-triethylamine have been determined in dimethyl-formamide (DMF)/acetonitrile (ACN)/acetone and aqueous mixtures of these solv

Convenient syntheses of 2-alkyl(Aryl)-4,5-diphenyloxazoles and 2-alkyl(Aryl)-4-phepyloxazoles

Pei, Weiwei,Li, Shaohui,Nie, Xiaoping,Li, Yiwei,Pei, Jian,Chen, Bingzi,Wu, Jie,Ye, Xiulin

, p. 1298 - 1304 (2007/10/03)

The synthetic methods to prepare 2-alkyl(aryl)-4,5-diphenyloxazoles and 2-alkyl(aryl)-4-phenyloxazoles were improved on the basis of a mechanistic study of oxazole formation from α-hydroxy ketones (carboxylic esters of benzoin and phenacyl alcohols). By these methods, seven trisubstituted oxazoles and twelve disubstituted oxazoles of the title compounds were prepared.

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