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126325-53-9

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126325-53-9 Usage

Description

3-AMINO-2-BROMO-6-PICOLINE is an organic compound that serves as a crucial intermediate in the synthesis of various chemical compounds. It is characterized by its unique molecular structure, which features an amino group, a bromine atom, and a picoline ring. This versatile compound is known for its potential applications across different industries due to its chemical properties.

Uses

Used in Organic Synthesis:
3-AMINO-2-BROMO-6-PICOLINE is used as a key intermediate for the synthesis of various organic compounds. Its unique structure allows it to be a valuable building block in the creation of new molecules with specific properties and functions.
Used in Agrochemical Industry:
In the agrochemical industry, 3-AMINO-2-BROMO-6-PICOLINE is used as a raw material for the development of new pesticides and other agricultural chemicals. Its incorporation into these products can enhance their effectiveness in protecting crops from pests and diseases.
Used in Pharmaceutical Industry:
3-AMINO-2-BROMO-6-PICOLINE is utilized as an intermediate in the synthesis of various pharmaceutical compounds. Its unique molecular structure can be manipulated to create new drugs with specific therapeutic properties, potentially leading to the development of novel treatments for various medical conditions.
Used in Dye Industry:
In the dye industry, 3-AMINO-2-BROMO-6-PICOLINE is used as a raw material for the production of different types of dyes. Its chemical properties make it suitable for the creation of dyes with specific color characteristics and stability, which can be applied in various industries such as textiles, plastics, and printing.

Check Digit Verification of cas no

The CAS Registry Mumber 126325-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,3,2 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126325-53:
(8*1)+(7*2)+(6*6)+(5*3)+(4*2)+(3*5)+(2*5)+(1*3)=109
109 % 10 = 9
So 126325-53-9 is a valid CAS Registry Number.

126325-53-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H64301)  3-Amino-2-bromo-6-methylpyridine, 98%   

  • 126325-53-9

  • 250mg

  • 196.0CNY

  • Detail
  • Alfa Aesar

  • (H64301)  3-Amino-2-bromo-6-methylpyridine, 98%   

  • 126325-53-9

  • 1g

  • 588.0CNY

  • Detail
  • Alfa Aesar

  • (H64301)  3-Amino-2-bromo-6-methylpyridine, 98%   

  • 126325-53-9

  • 5g

  • 2352.0CNY

  • Detail

126325-53-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-6-methylpyridin-3-amine

1.2 Other means of identification

Product number -
Other names 2-bromo-6-methylpyridin-3-amine

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:126325-53-9 SDS

126325-53-9Upstream product

126325-53-9Relevant articles and documents

Substituent-Controlled Tailoring of Chalcogen-Bonded Supramolecular Nanoribbons in the Solid State

Biot, Nicolas,Romito, Deborah,Bonifazi, Davide

, p. 536 - 543 (2020/12/21)

In this work, we design and synthesize supramolecular 2,5-substituted chalcogenazolo[5,4-β]pyridine (CGP) synthons arranging in supramolecular ribbons at the solid state. A careful choice of the combination of substituents at the 2- and 5-positions on the

Bromination of Pyridines. II. Bromination of Aminopicolines

Dunn, A. D.,Currie, A.,Hayes, L. E.

, p. 369 - 374 (2007/10/02)

The bromination of all ten possible aminopicolines 1-10 was investigated.In general, the major brominated product was that corresponding to electrophilic attack at the sites para or ortho to the amino group.

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