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152849-72-4

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152849-72-4 Usage

General Description

BENZOIC ACID, 5-BROMO-2,4-DIMETHYL-, METHYL ESTER is a chemical compound used in various industries, including pharmaceuticals, fragrances, and agrochemicals. It is a methyl ester derivative of 5-Bromo-2,4-dimethylbenzoic acid, which is known for its antimicrobial and antifungal properties. The methyl ester form is often used as a flavoring agent and preservative in food and beverages. It is also utilized as an intermediate in the production of other chemical compounds. The compound should be handled and stored with caution, as it may pose health and environmental risks if not managed properly.

Check Digit Verification of cas no

The CAS Registry Mumber 152849-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,8,4 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 152849-72:
(8*1)+(7*5)+(6*2)+(5*8)+(4*4)+(3*9)+(2*7)+(1*2)=154
154 % 10 = 4
So 152849-72-4 is a valid CAS Registry Number.

152849-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 5-bromo-2,4-dimethylbenzoate

1.2 Other means of identification

Product number -
Other names 5-Brom-2,4-dimethyl-benzoesaeure-methylester

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:152849-72-4 SDS

152849-72-4Relevant articles and documents

Synthesis of Sterically Hindered 1,3-Connected Polyarylmethanes

Rajca, Andrzej,Janicki, Slawomir

, p. 7099 - 7107 (2007/10/02)

Sterically hindered 1,3-connected polyarylmethanes were prepared by repetitive additions of aryllithiums to carbonyl compounds.Synthetic routes with various degree of convergence were used.Variable temperature NMR spectroscopy, in conjunction with other t

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