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Benzoic acid, 4-methyl-, 2-acetyl-4-chlorophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88952-03-8

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88952-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88952-03-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,5 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88952-03:
(7*8)+(6*8)+(5*9)+(4*5)+(3*2)+(2*0)+(1*3)=178
178 % 10 = 8
So 88952-03-8 is a valid CAS Registry Number.

88952-03-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-acetyl-4-chlorophenyl) 4-methylbenzoate

1.2 Other means of identification

Product number -
Other names 2-acetyl-4-chlorophenyl 4-methylbenzoate

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:88952-03-8 SDS

88952-03-8Relevant academic research and scientific papers

Directing group assisted copper-catalyzed chemoselective O-aroylation of phenols and enols using alkylbenzenes

Rout, Saroj Kumar,Guin, Srimanta,Banerjee, Arghya,Khatun, Nilufa,Gogoi, Anupal,Patel, Bhisma K.

supporting information, p. 4106 - 4109 (2013/09/12)

By using alkylbenzenes as aroyl surrogates, copper(II) catalyzed chemoselective O-aroylations of 1,3-dicarbonyl compounds and phenolic-OH ortho to carbonyl (-CHO,-COR) groups have been achieved. A dual mechanism operating in tandem for these transformations has been supported by a crossover experiment.

The Synthesis and Spectroscopic Properties of Flavones: Special Mass Spectral Characteristics of 3-Methylflavones

Letcher, Roy M.

, p. 2901 - 2929 (2007/10/02)

The synthesis of twenty one methyl-, methoxy-, nitro- and halogen-substituted 3-methylflavones is described, and their spectroscopic characteristics are reported.In contrast to the mass spectra of 3-unsubstituted flavones, the most abundant ion exhibited

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