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3-Amino-4,6-dibromopyridine is a pyridine derivative with the molecular formula C5H4Br2N2, featuring two bromine atoms and an amino group attached to the pyridine ring. This chemical compound has potential applications in pharmaceuticals and agrochemicals, serving as a building block in the synthesis of various organic compounds and as an intermediate in the production of active pharmaceutical ingredients and agrochemicals. Its potential biological activities have garnered interest among researchers in medicinal chemistry and chemical biology.

50786-37-3

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50786-37-3 Usage

Uses

Used in Pharmaceutical Industry:
3-Amino-4,6-dibromopyridine is used as a building block for the synthesis of various organic compounds, contributing to the development of new pharmaceuticals. Its unique structure allows for the creation of diverse molecules with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 3-Amino-4,6-dibromopyridine is utilized as an intermediate in the production of active ingredients for pesticides and other agrochemical products. Its presence in these compounds can enhance their effectiveness in controlling pests and diseases in agriculture.
Used in Medicinal Chemistry Research:
3-Amino-4,6-dibromopyridine is used as a research compound in medicinal chemistry, where its potential biological activities are studied. Researchers explore its interactions with biological targets to understand its therapeutic potential and develop new drugs based on its structure.
Used in Chemical Biology Studies:
In the field of chemical biology, 3-Amino-4,6-dibromopyridine is employed as a tool compound to investigate biological processes and mechanisms. Its unique chemical properties allow researchers to probe and manipulate biological systems, contributing to a deeper understanding of life sciences.

Check Digit Verification of cas no

The CAS Registry Mumber 50786-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,8 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 50786-37:
(7*5)+(6*0)+(5*7)+(4*8)+(3*6)+(2*3)+(1*7)=133
133 % 10 = 3
So 50786-37-3 is a valid CAS Registry Number.

50786-37-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dibromopyridin-3-amine

1.2 Other means of identification

Product number -
Other names 4,6-dibromo-pyridin-3-ylamine

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:50786-37-3 SDS

50786-37-3Downstream Products

50786-37-3Relevant academic research and scientific papers

COMPOUND HAVING BET INHIBITORY ACTIVITY AND PREPARATION METHOD AND USE THEREFOR

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Paragraph 0258, (2020/12/22)

The invention relates to the field of pharmaceutical chemistry. Specifically, the present invention relates to a series of BET (bromodomain and extra-terminal domain) inhibitors having a novel structure, particularly inhibitors targeting BRD4 (Bromodomain-containing protein 4), and a preparation method and use therefor. The structure thereof is shown in the following general formula (I). Said compounds or a stereoisomer, racemate, geometric isomer, tautomer, prodrug, hydrate, solvate, or crystal form thereof, or a pharmaceutically acceptable salt thereof, and the pharmaceutical compsosition thereof can be used for the treatment and/or prevention of related diseases mediated by bromodomain proteins.

HETEROARYL COMPOUNDS USEFUL AS RAF KINASE INHIBITORS

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Page/Page column 136, (2010/08/04)

The present invention provides compounds of formula (I) useful as inhibitors of Raf protein kinase. The present invention also provides compositions thereof, and methods of treating Raf -mediated diseases.

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