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Methyl 5-chloro-6-methoxynicotinate is a chemical compound that is a derivative of nicotinic acid, known for its various biological and pharmacological activities. It is characterized by the presence of a chlorine atom at the 5th position and a methoxy group at the 6th position of the nicotinic acid molecule.
Used in Pharmaceutical Industry:
Methyl 5-chloro-6-methoxynicotinate is used as an intermediate in the synthesis of various pharmaceuticals for its potential as an anti-inflammatory and analgesic agent.
Used in Agrochemical Industry:
Methyl 5-chloro-6-methoxynicotinate is used as an insecticide and fungicide due to its insecticidal and fungicidal properties.
Used in Chemical Synthesis:
Methyl 5-chloro-6-methoxynicotinate is used as a valuable building block for the development of new compounds with potential therapeutic and agricultural applications, owing to its unique structure and properties.

220656-93-9

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220656-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220656-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,6,5 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 220656-93:
(8*2)+(7*2)+(6*0)+(5*6)+(4*5)+(3*6)+(2*9)+(1*3)=119
119 % 10 = 9
So 220656-93-9 is a valid CAS Registry Number.

220656-93-9SDS

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 methyl 5-chloro-6-methoxypyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 5-chloro-6-methoxynicotinate

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:220656-93-9 SDS

220656-93-9Relevant academic research and scientific papers

Selective alkoxycarbonylation of 2,3-dichloropyridines

Bessard, Yves,Roduit, Jean Paul

, p. 393 - 404 (2007/10/03)

2,3-Dichloropyridines undergo a motto- or a dicarbonylation in the presence of carbon monoxide, an alcohol and a palladium catalyst, affording selectively either alkyl 3-chloropicolinates, or dialkyl pyridine-2,3- dicarboxylates in good yields, depending on the reaction conditions.

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