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1000018-58-5

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1000018-58-5 Usage

General Description

2-Chloro-3,5-dibromo-6-methylpyridine is an organic compound with the molecular formula C6H4Br2ClN. It is a derivative of pyridine and contains chlorine and bromine atoms. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and properties make it a valuable building block for the production of various complex organic compounds. 2-Chloro-3,5-dibromo-6-methylpyridine is a versatile and important chemical compound with a wide range of industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1000018-58-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,0,1 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1000018-58:
(9*1)+(8*0)+(7*0)+(6*0)+(5*0)+(4*1)+(3*8)+(2*5)+(1*8)=55
55 % 10 = 5
So 1000018-58-5 is a valid CAS Registry Number.

1000018-58-5SDS

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 3,5-Dibromo-2-chloro-6-methylpyridine

1.2 Other means of identification

Product number -
Other names 2-Chloro-3,5-dibromo-6-methylpyridine

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:1000018-58-5 SDS

1000018-58-5Relevant articles and documents

P38 MAP kinase inhibitors. part 1: Design and development of a new class of potent and highly selective inhibitors based on 3,4-dihydropyrido[3,2-d]pyrimidone scaffold

Natarajan, Swaminathan R.,Wisnoski, David D.,Singh, Suresh B.,Stelmach, John E.,O'Neill, Edward A.,Schwartz, Cheryl D.,Thompson, Chris M.,Fitzgerald, Catherine E.,O'Keefe, Stephen J.,Kumar, Sanjeev,Hop, Cornelis E. C. A.,Zaller, Dennis M.,Schmatz, Dennis M.,Doherty, James B.

, p. 273 - 276 (2003)

A new class of p38 antagonists based on 3,4-dihydropyrido[3,2,-d]pyrimidine scaffold has been developed. These inhibitors exhibit unprecedented selectivity towards p38 over other very closely related kinases. Compounds 25, 33, and 34 were identified as be

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