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2-bromo-N-methylpyridin-3-amine is a chemical compound characterized by its molecular formula C6H7BrN2. It is a pyridine derivative, featuring a six-membered heterocyclic aromatic ring with one nitrogen atom, to which a bromine atom and a methyl group are attached at the 3 position. 2-bromo-N-methylpyridin-3-amine is recognized for its structural properties and reactivity, making it a valuable intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries.

872492-60-9

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872492-60-9 Usage

Uses

Used in Pharmaceutical Industry:
2-bromo-N-methylpyridin-3-amine is utilized as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of biologically active compounds. Its unique structural features and reactivity allow for the creation of new drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-bromo-N-methylpyridin-3-amine serves as an intermediate in the production of agrochemicals, aiding in the development of compounds that can be used in pest control and crop protection, thereby enhancing agricultural productivity.
Used in Medicinal Chemistry and Drug Discovery:
2-bromo-N-methylpyridin-3-amine is employed as a building block in medicinal chemistry and drug discovery due to its potential to form biologically active molecules. Its functional groups and structural versatility facilitate the design and synthesis of novel compounds with specific pharmacological properties.
Used in the Development of Novel Materials and Chemical Processes:
Beyond its applications in synthesis, 2-bromo-N-methylpyridin-3-amine is also used in the development of new materials and chemical processes, capitalizing on its functional groups to create innovative products and improve existing chemical technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 872492-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,4,9 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 872492-60:
(8*8)+(7*7)+(6*2)+(5*4)+(4*9)+(3*2)+(2*6)+(1*0)=199
199 % 10 = 9
So 872492-60-9 is a valid CAS Registry Number.
InChI:InChI=1S/C6H7BrN2/c1-8-5-3-2-4-9-6(5)7/h2-4,8H,1H3

872492-60-9SDS

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-N-methylpyridin-3-amine

1.2 Other means of identification

Product number -
Other names (2-BROMO-PYRIDIN-3-YL)-METHYL-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:872492-60-9 SDS

872492-60-9Relevant academic research and scientific papers

Practical way to imidazo[4,5-b] and [4,5-c]pyridine-2-ones via cascade ureidation/palladium-catalyzed cyclization

Lach, Franck,Koza, Patrice

, p. 491 - 495 (2012/10/29)

We developed an efficient one-pot tandem carbamoyl chloride amination and palladium-catalyzed intramolecular urea cyclization, which furnished high-throughput access to imidazo[4,5-b]pyridine-2-one and related imidazo[4,5-c]pyridine-2-one ring systems. Mo

A valuable synthesis of pyrrolo[1,2-a]quinoxalines, indolo[1,2-a] quinoxalines and their aza-analogues by palladium-catalyzed intramolecular carbon-nitrogen bond formation

Abbiati, Giorgio,Beccalli, Egle M.,Broggini, Gianluigi,Paladino, Giuseppe,Rossi, Elisabetta

, p. 2881 - 2886 (2007/10/03)

A novel and efficient method for the construction of pyrrolo[1,2-a] quinoxalines, indolo[1,2-a]quinoxalines and their aza-analogues is described. The reaction involves a Pd-catalyzed intramolecular cyclization as the key step and provides the desired prod

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