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885267-14-1

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885267-14-1 Usage

General Description

(6-chloropyridin-2-yl)acetic acid is a chemical compound with the molecular formula C7H6ClNO2. It is a derivative of pyridine and is commonly used in the pharmaceutical industry as an intermediate for the synthesis of various compounds. This chemical is known for its potential use in the treatment of various diseases and conditions, including inflammation and pain. Its structure and properties make it a useful building block for the development of new pharmaceutical drugs. Additionally, it has been studied for its potential antimicrobial and antiviral activities, making it a versatile and important compound in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 885267-14-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,6 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 885267-14:
(8*8)+(7*8)+(6*5)+(5*2)+(4*6)+(3*7)+(2*1)+(1*4)=211
211 % 10 = 1
So 885267-14-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClNO2/c8-6-3-1-2-5(9-6)4-7(10)11/h1-3H,4H2,(H,10,11)

885267-14-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(6-chloropyridin-2-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 6-chloro-2-pyridylacetic 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:885267-14-1 SDS

885267-14-1Relevant articles and documents

Catalytic asymmetric cyclopropanation of heteroaryldiazoacetates

Davies,Townsend

, p. 6595 - 6603 (2007/10/03)

Rh2(S-DOSP)4-catalyzed decomposition of heteroaryldiazoacetates in the presence of styrene results in highly diastereoselective and enantioselective cyclopropanations. Heteroaryldiazoacetates containing both electron-rich and electron-deficient heterocycles, such as thiophene, furan, pyridine, indole, oxazole, isoxazole, and benzoxazole, are effective in this chemistry. These studies broaden the range of diazo compounds containing both electron-withdrawing and electron-donating groups, which undergo highly diastereoselective cyclopropanations.

2-Pyridylhydrazides

-

, (2008/06/13)

2-Pyridylhydrazides useful as antiinflammatory agents.

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