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52833-93-9

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52833-93-9 Usage

General Description

2-Amino-5-chloropyridine-3-carboxylic acid is a chemical compound with the molecular formula C6H5ClN2O2. It is a derivative of pyridine and aminopyridine, containing both an amino group and a carboxylic acid group. 2-Amino-5-chloropyridine-3-carboxylic acid is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It has been studied for its potential antimicrobial and anticancer properties, making it a valuable molecule in the development of new drugs. 2-Amino-5-chloropyridine-3-carboxylic acid is a versatile chemical that is utilized in various fields, showcasing its importance in organic synthesis and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 52833-93-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,3 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52833-93:
(7*5)+(6*2)+(5*8)+(4*3)+(3*3)+(2*9)+(1*3)=129
129 % 10 = 9
So 52833-93-9 is a valid CAS Registry Number.

52833-93-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-5-chloropyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-azanyl-5-chloranyl-pyridine-3-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:52833-93-9 SDS

52833-93-9Downstream Products

52833-93-9Relevant articles and documents

Regioselective palladium-catalyzed Suzuki–Miyaura coupling reaction of 2,4,6-trihalogenopyrido[2,3-d]pyrimidines

Riadi, Yassine,Lazar, Sa?d,Guillaumet, Gérald

, p. 294 - 298 (2019/02/25)

An effective, regioselective, and novel strategy to the access of 2,4,6-trisubstituted pyrido[2,3-d]pyrimidines is developed from the corresponding 2,4,6-trihalogenopyrido[2,3-d]pyrimidine through a Suzuki–Miyaura coupling reaction involving a novel regioselective halogen discrimination.

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