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178421-21-1

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178421-21-1 Usage

General Description

Ethyl 6-chloro-5-methylpicolinate is a chemical compound with the molecular formula C8H9NO2Cl. It is a derivative of picolinic acid and is commonly used in organic synthesis as a building block for the production of pharmaceuticals and agrochemicals. The compound contains a chlorine atom and a methyl group attached to a pyridine ring, making it a valuable intermediate in the development of various compounds with biological activity. Ethyl 6-chloro-5-methylpicolinate is known for its versatile reactivity and is used as a key starting material in the synthesis of pyridine-based heterocycles, which have potential applications in medicinal chemistry research.

Check Digit Verification of cas no

The CAS Registry Mumber 178421-21-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,4,2 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 178421-21:
(8*1)+(7*7)+(6*8)+(5*4)+(4*2)+(3*1)+(2*2)+(1*1)=141
141 % 10 = 1
So 178421-21-1 is a valid CAS Registry Number.

178421-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 6-chloro-5-methylpyridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-ethoxycarbonyl-5-methyl-6-chloro-pyridine

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:178421-21-1 SDS

178421-21-1Relevant articles and documents

A new pathway to substituted 6-chloro-2-pyridinecarboxylic acid derivatives from the reaction of 4,6-dichloro-2-oxa-5-azabicyclo[2.2.2]oct-5-en-3-ones with nucleophiles

Dubois, Kristof J.,Hoornaert, Georges J.

, p. 6997 - 7002 (1996)

Reaction of alcohols or amines with 4,6-dichloro-2-oxa-5-azabicyclo[2.2.2]oct-5-en-3-ones gives direct conversion into (3,(4,))5-substituted 6-chloro-2-pyridinecarboxylic acid derivatives via selective lactone cleavage followed by rapid elimination of HCl and H2O in the presence of DBU. Copyright

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