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65996-18-1

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65996-18-1 Usage

General Description

2-Bromo-5-Methylnicotinonitrile is a chemical compound with the molecular formula C8H6BrN2. It is a derivative of nicotinonitrile, which is a type of pyridine compound. This chemical is commonly used in pharmaceutical industry for the synthesis of various pharmaceutical compounds. It is an important intermediate in the production of nicotinamide riboside chloride, which has shown potential in the treatment of conditions like obesity and diabetes. 2-Bromo-5-Methylnicotinonitrile is also used as a building block in the synthesis of other important organic compounds and is an important reagent in organic chemistry. This chemical has a bromine atom and a nitrile group, making it a valuable component in the creation of diverse chemical structures.

Check Digit Verification of cas no

The CAS Registry Mumber 65996-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,9 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65996-18:
(7*6)+(6*5)+(5*9)+(4*9)+(3*6)+(2*1)+(1*8)=181
181 % 10 = 1
So 65996-18-1 is a valid CAS Registry Number.

65996-18-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-5-methylpyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-Brom-5-methyl-nicotinnitril

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:65996-18-1 SDS

65996-18-1Downstream Products

65996-18-1Relevant articles and documents

Synthesis and Reactivity Profile of Ylidenemalononitrile Enamines and Their Ester Analogs Towards Electrophiles and Nucleophiles

Longstreet, Ashley R.,Rivalti, Daniel,McQuade, D. Tyler

, p. 8583 - 8596 (2015/09/15)

Herein, we describe the synthesis and reactivity of enamines derived from ylidenemalononitriles and ylidenecyanoacetates. The enamine scope was expanded by (1) increasing yields of aldehyde-derived ylidenemalononitriles, (2) incorporating silyl functional

DIRECT SUBSTITUTION OF A METHOXY GROUP BY BROMINE IN 2-METHOXYPYRIDINE-3-CARBONITRILES: A SYNTHESIS OF 2-BROMOPYRIDINE-3-CARBONITRILES

Victory, P.,Borrell, J. I.,Castejon, P.,Martinez-Teipel, B.,Vidal-Ferran, A.

, p. 625 - 628 (2007/10/02)

The treatment of a wide variety of 2-methoxypyridine-3-carbonitriles with phosphorus oxytribromide in the presence of pyridinium hydrobromide and phosphoric acid yields directly the corresponding pyridine system in which the methoxy group has been substit

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