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112930-39-9

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112930-39-9 Usage

General Description

3-Bromo-5-isopropylbenzoic acid is a compound with the molecular formula C10H11BrO2. It is a derivative of benzoic acid, with a bromine atom and an isopropyl group attached to the benzene ring. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential anti-inflammatory and antimicrobial properties. The presence of the bromine atom in its structure makes 3-Bromo-5-isopropylbenzoic acid a valuable building block for the synthesis of diverse organic compounds. Overall, this compound has important applications in the fields of medicine, pharmaceuticals, and organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 112930-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,3 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112930-39:
(8*1)+(7*1)+(6*2)+(5*9)+(4*3)+(3*0)+(2*3)+(1*9)=99
99 % 10 = 9
So 112930-39-9 is a valid CAS Registry Number.

112930-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-5-propan-2-ylbenzoic acid

1.2 Other means of identification

Product number -
Other names 3-Bromo-5-isopropylbenzoic acid

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:112930-39-9 SDS

112930-39-9Upstream product

112930-39-9Relevant articles and documents

Steric Effects. Internal Rotation of 1-Aryl-8-phenylnaphthalenes

Cosmo, Robert,Sternhell, Sever

, p. 1107 - 1126 (2007/10/02)

A general, albeit low-yielding, synthesis of 1-aryl-8-phenylnaphthalenes was devised and used to prepare three 1-(3'-X-5'-isopropylphenyl)-8-phenylnaphthalenes (X = H, F, Br).Activation parameters for the rotation of the 3'-X-5'-isopropylphenyl group were

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