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853179-74-5

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853179-74-5 Usage

General Description

2-Bromo-6-methylpyridine-3-carboxaldehyde is a chemical compound with the formula C8H7BrNO. It is a derivative of pyridine and is commonly used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. 2-Bromo-6-methylpyridine-3-carboxaldehyde is known for its strong odor and is typically handled and stored with caution due to its potential hazards. It is also used in the manufacturing of dyes, pigments, and flavor and fragrance compounds. The presence of the bromine atom in its structure provides unique reactivity and properties, making it a valuable building block in the synthesis of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 853179-74-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,1,7 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 853179-74:
(8*8)+(7*5)+(6*3)+(5*1)+(4*7)+(3*9)+(2*7)+(1*4)=195
195 % 10 = 5
So 853179-74-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H6BrNO/c1-5-2-3-6(4-10)7(8)9-5/h2-4H,1H3

853179-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-6-methylpyridine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-Pyridinecarboxaldehyde,2-bromo-6-methyl

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:853179-74-5 SDS

853179-74-5Relevant articles and documents

A new approach to the 1,10-phenanthroline core

Chelucci, Giorgio,Addis, Daniele,Baldino, Salvatore

, p. 3359 - 3362 (2008/02/12)

A protocol for the synthesis of substituted 1,10-phenanthrolines is reported. The phenanthroline scaffold has been obtained constructing the central cycle starting from two pyridine rings. The method is hinged upon the intramolecular coupling of cis-1,2-di(2-bromo-3-pyridyl)ethenes that are in turn obtained from the Wittig reaction of 2-bromonicotinaldehydes with phosphonium salts prepared from 2-bromo-3-(bromomethyl)pyridines. Yields up to 75% have been obtained.

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