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5407-86-3

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5407-86-3 Usage

General Description

2-Amino-3,5-dibromo-4,6-dimethylpyridine is a chemical compound with the molecular formula C7H8Br2N2. It is a pyridine derivative and belongs to the class of organic compounds known as aminopyridines. 2-Amino-3,5-dibromo-4,6-dimethylpyridine is primarily used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It is also used as a building block in the production of agrochemicals and as a reagent in chemical research. 2-Amino-3,5-dibromo-4,6-dimethylpyridine is a highly reactive compound and should be handled with caution due to its potential toxicity and environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 5407-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5407-86:
(6*5)+(5*4)+(4*0)+(3*7)+(2*8)+(1*6)=93
93 % 10 = 3
So 5407-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H8Br2N2/c1-3-5(8)4(2)11-7(10)6(3)9/h1-2H3,(H2,10,11)

5407-86-3SDS

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-4,6-dimethylpyridin-2-amine

1.2 Other means of identification

Product number -
Other names 6-amino-3,5-dibromo-2,4-lutidine

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:5407-86-3 SDS

5407-86-3Relevant articles and documents

-

Mariella,Belcher

, p. 1916,1918 (1952)

-

Regio- and stereoselective syntheses of the natural product CCR5 antagonist anibamine and its three olefin isomers

Zhang, Feng,Zaidi, Saheem,Haney, Kendra M.,Kellogg, Glen E.,Zhang, Yan

experimental part, p. 7945 - 7952 (2011/11/30)

The syntheses of the natural product anibamine and its three olefin isomers have been achieved concisely and efficiently via highly regio- and stereoselective reactions. The crucial steps included a regioselective palladium-catalyzed alkynylation by Sonogashira coupling and a stereoselective Suzuki coupling. Further conformation analyses and in vitro calcium mobilization studies were carried out to characterize the compounds' biological properties.

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