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Product Information

Product Name
2-Amino-3-chloropyridine
Brand Name
Chem Impex
Product Number
17023
CAS
39620-04-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
693267
IUPAC Name
3-chloropyridin-2-amine
InChI Key
RZJPBQGRCNJYBU-UHFFFAOYSA-N
SMILES
C1=CC(=C(N=C1)N)Cl

Application

2-Amino-3-chloropyridine is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and antimicrobial agents.

Agricultural Chemicals: It is used in the formulation of agrochemicals, contributing to the development of herbicides and pesticides that help improve crop yields and protect plants from pests.

Material Science: The compound is explored in the creation of novel materials, such as polymers and coatings, which can enhance durability and resistance to environmental factors.

Research in Organic Chemistry: It acts as a building block in organic synthesis, allowing chemists to create more complex molecules for various applications, including dyes and pigments.

Biochemical Research: 2-Amino-3-chloropyridine is investigated for its potential role in enzyme inhibition studies, aiding researchers in understanding metabolic pathways and disease mechanisms.

References

Development of Nurr1 agonists from amodiaquine by scaffold hopping and fragment growing

Publication Name: Communications Chemistry
Publication Date: 2024-06-29
DOI: 10.1038/s42004-024-01224-0

BMS794833 inhibits macrophage efferocytosis by directly binding to MERTK and inhibiting its activity

Publication Name: Experimental & Molecular Medicine
Publication Date: 2022-09-02
DOI: 10.1038/s12276-022-00840-x

Modern methods for the synthesis of δ-carbolines

Publication Name: Russian Chemical Bulletin
Publication Date: 2019-04
DOI: 10.1007/s11172-019-2475-6

Pushing the Limits of Detection of Weak Binding Using Fragment-Based Drug Discovery: Identification of New Cyclophilin Binders

Publication Name: Journal of Molecular Biology
Publication Date: 2017-08-04
DOI: 10.1016/j.jmb.2017.06.016

Oxyfunctionalization of pyridine derivatives using whole cells of Burkholderia sp. MAK1

Publication Name: Scientific Reports
Publication Date: 2016-12-16
DOI: 10.1038/srep39129