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58553-54-1

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58553-54-1 Usage

General Description

Ethyl 3-(chloromethyl)isonicotinate is a chemical compound with the molecular formula C10H11ClNO2. It is a pale yellow liquid with a molecular weight of 211.65 g/mol. ETHYL 3-(CHLOROMETHYL)ISONICOTINATE is commonly used in the synthesis of pharmaceuticals and agrochemicals. The chloromethyl group in the molecule makes it useful for introducing the isonicotinic acid moiety into various organic molecules. Ethyl 3-(chloromethyl)isonicotinate has been studied for its potential antitumor and antimicrobial properties. It is important to handle this compound with care, as it is considered to be harmful if swallowed or inhaled, and can cause skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 58553-54-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,5 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58553-54:
(7*5)+(6*8)+(5*5)+(4*5)+(3*3)+(2*5)+(1*4)=151
151 % 10 = 1
So 58553-54-1 is a valid CAS Registry Number.

58553-54-1SDS

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 ethyl 3-(chloromethyl)pyridine-4-carboxylate

1.2 Other means of identification

Product number -
Other names 3-chloromethyl-4-pyridine carboxylic acid ethyl 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:58553-54-1 SDS

58553-54-1Relevant articles and documents

Preparation of some Thiopyranopyridine Derivatives

Clarke, Kenneth,Goulding, John,Scrowston, Richard M.

, p. 1501 - 1505 (2007/10/02)

In the first systematic study of thiopyranopyridines in which the sulphur atom is separated from the pyridine ring by one carbon atom, the four isomeric enol esters, ethyl 5-hydroxy-8H-thiopyranopyridine-6-carboxylate (4b), ethyl 8-hydroxy-5H-thiopyranopyridine-7-carboxylate (5b), and ethyl 4-hydroxy-1H-thiopyrano- and pyridine-3-carboxylate (6b) and (7b), have been synthesised.Improved methods for the preparation of their pyridine precursors are described.With phenylhydrazine, the enol esters (4b) - (7b) give condensed pyrazole derivatives (15) - (18), which have dipolar structures; with hot mineral acid they undergo decarboxylative hydrolysis, to give the corresponding oxothiopyranopyridines (4a) - (7a).

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