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1000017-92-4 Usage

General Description

2-Chloro-3,5-dibromo-4-methylpyridine is a chemical compound often used in pharmaceuticals and organic synthesis due to its properties as a functionalized pyridine. This aromatic organic compound has three distinct substituent groups on its pyridine ring: a chlorine atom, a methyl group and two bromine atoms, which give it unique chemical reactivity. Its molecular formula is C6H4Br2ClN and it's characterized by its yellowish appearance. As with many organic chemicals, safety precautions must be followed while handling this compound to avoid any potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 1000017-92-4 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 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1000017-92:
54 % 10 = 4
So 1000017-92-4 is a valid CAS Registry Number.



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


1.1 GHS Product identifier

Product name 2-Chloro-3,5-dibromo-4-methylpyridine

1.2 Other means of identification

Product number -

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:1000017-92-4 SDS

1000017-92-4Downstream Products

1000017-92-4Relevant articles and documents

Iron(II)-Based Metalloradical Activation: Switch from Traditional Click Chemistry to Denitrogenative Annulation

Roy, Satyajit,Khatua, Hillol,Das, Sandip Kumar,Chattopadhyay, Buddhadeb

supporting information, p. 11439 - 11443 (2019/07/17)

A unique concept for the intermolecular denitrogenative annulation of 1,2,3,4-tetrazoles and alkynes was discovered by using a catalytic amount of Fe(TPP)Cl and Zn dust. The reaction precludes the traditional, more favored click reaction between an organic azide and alkynes, and instead proceeds by an unprecedented metalloradical activation. The method is anticipated to advance access to the construction of important basic nitrogen heterocycles, which will in turn enable discoveries of new drug candidates.

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