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324028-95-7

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324028-95-7 Usage

Uses

6-Chloro-4-methylpyridine-2-carboxylic acid

Check Digit Verification of cas no

The CAS Registry Mumber 324028-95-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,4,0,2 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 324028-95:
(8*3)+(7*2)+(6*4)+(5*0)+(4*2)+(3*8)+(2*9)+(1*5)=117
117 % 10 = 7
So 324028-95-7 is a valid CAS Registry Number.

324028-95-7 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H63584)  6-Chloro-4-methylpyridine-2-carboxylic acid, 95%   

  • 324028-95-7

  • 250mg

  • 326.0CNY

  • Detail
  • Alfa Aesar

  • (H63584)  6-Chloro-4-methylpyridine-2-carboxylic acid, 95%   

  • 324028-95-7

  • 1g

  • 980.0CNY

  • Detail
  • Alfa Aesar

  • (H63584)  6-Chloro-4-methylpyridine-2-carboxylic acid, 95%   

  • 324028-95-7

  • 5g

  • 3920.0CNY

  • Detail

324028-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-CHLORO-4-METHYLPYRIDINE-2-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 6-chloro-4-methyl-pyridine-2-carboxylic acid

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:324028-95-7 SDS

324028-95-7Relevant articles and documents

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

-

, (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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