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4-Chloro-6-Methoxy-pyridine-2-carboxylic acid is a pyridine derivative with the molecular formula C7H6ClNO3. It features a chloro and methoxy group on the 4th and 6th carbon atoms, respectively, and a carboxylic acid functionality on the 2nd carbon atom of the pyridine ring. This chemical compound is widely recognized for its potential biological activities and is frequently utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as a building block in the creation of various organic compounds.

204378-34-7

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204378-34-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-6-Methoxy-pyridine-2-carboxylic acid is used as an intermediate in the synthesis of pharmaceuticals for its potential biological activities. It plays a crucial role in the development of new drugs, contributing to the advancement of medicine and healthcare.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Chloro-6-Methoxy-pyridine-2-carboxylic acid is employed as an intermediate in the synthesis of agrochemicals. Its involvement in the production of these chemicals helps to improve agricultural yields and protect crops from pests and diseases.
Used in Organic Synthesis:
4-Chloro-6-Methoxy-pyridine-2-carboxylic acid is used as a building block in the synthesis of various organic compounds. Its unique structure and functional groups make it a valuable component in the creation of a wide range of organic molecules for diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 204378-34-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,3,7 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 204378-34:
(8*2)+(7*0)+(6*4)+(5*3)+(4*7)+(3*8)+(2*3)+(1*4)=117
117 % 10 = 7
So 204378-34-7 is a valid CAS Registry Number.

204378-34-7SDS

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 4-chloro-6-methoxypyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-chloro-6-methoxy-pyridine-2-carboxylate

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:204378-34-7 SDS

204378-34-7Relevant academic research and scientific papers

PIPERAZINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLU5 RECEPTORS

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, (2013/07/05)

This invention relates to compounds of formula (I) their use as positive allosteric modulators of mGlu5 receptor activity, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of neurological and psychiatric disorders associated with glutamate dysfunction such as schizophrenia or cognitive decline such as dementia or cognitive impairment. R1, R2, R3, R4, Q have meanings given in the description.

NOVEL COMPOUNDS

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, (2013/06/28)

This invention relates to compounds of formula I their use as positive allosteric modulators of mGlu5 receptor activity, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of neurological and psychiatric disorders associated with glutamate dysfunction such as schizophrenia or cognitive decline such as dementia or cognitive impairment. R1, R2, R3, R4, Q have meanings given in the description.

N-(phenylsulfonyl)picolinamide derivatives, process for producing the same, and herbicide

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, (2008/06/13)

A herbicide containing as the active ingredient an N-(henylsulfonyl)picolinamide derivative represented by general formula (I) wherein X reprcsents a halogeno, a C1-4 alkyl, a C1-4 haloalkyl, a C1-4 alkoxy, a C1-4 haloalkoxy, a (C1-4 alkoxy)carbonyl, a [di(C1-4 alkyl)amino]sulfonyl, an [N—(C1-4 alkyl)-N—(C1-4 alkoxy)amino]sulfonyl, a (C1-4 alkylamino)sulfonyl, a C1-4 alkylthio, a C1-4 alkylsulfinyl, a C1-4 alkylsulfonyl, or nitro; n is an integer of 0 to 5; Y represets a halogeno, a C1-4 alkyl, a C1-4 haloalkyl, a C1-4 alkoxy, C1-4 haloalkoxy, a C1-4 alkylthio, a C1-4 haloalkylthio, amino, a C1-4 alkylamino, a di(C1-4 alkyl)amino, a (C1-4 alkoxy) C1-4 alkyl, a (C1-4 alkylthio) C1-4 alkyl, or nitro; and m is an integer of 0 to 4. This active ingredient is synthesized by condensing a substituted picolinic acid with a substituted benzenesulfonamide under dehydration, or by reacting the phenyl ester of a substituted picolinic acid with a substituted benzenesulfonamide in the presence of a basic compound.

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