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855473-50-6

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855473-50-6 Usage

Uses

Methyl 2-(1-Bromomethylcyclopropyl)acetate is a reactant in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 855473-50-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,4,7 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 855473-50:
(8*8)+(7*5)+(6*5)+(5*4)+(4*7)+(3*3)+(2*5)+(1*0)=196
196 % 10 = 6
So 855473-50-6 is a valid CAS Registry Number.

855473-50-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-bromomethyl-cyclopropyl)-acetic acid methyl ester

1.2 Other means of identification

Product number -
Other names 2-(1-BROMIDEMETHYL-CYCLOPROPYL)ACETIC ACID METHYL 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:855473-50-6 SDS

855473-50-6Relevant articles and documents

Montelukast side chain intermediate and preparing method thereof

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Paragraph 0051; 0052, (2016/11/24)

The invention belongs to the field of medical chemistry, and particularly relates to a montelukast side chain intermediate and a preparing method thereof. A provided intermediate compound is 6-halogenated methyl-5,7-dioxaspiro[2,5] octane, wherein 1,1-cyclopropyl dimethyl carbinol serving as a starting material and 2-halogeno-1,1-dimethoxyethane are subjected to a transacetalation reaction under solid acid catalysis to obtain 6-halogenated methyl-5,7-dioxaspiro[2,5] octane, the intermediate is treated with organic alkali and then hydrolyzed with a water solution containing acetic acid to obtain monoacetylated protected diol. The problems that monoacetylated protected diol is poor in selectivity, and diol loss is serious are solved, the availability of the raw materials is improved, and the montelukast side chain intermediate can be synthesized economically and conveniently.

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