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Sku CI27934_25_G
Chem Impex
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Product Information

Product Name
2-Amino-4-ethylpyridine
Brand Name
Chem Impex
Product Number
27934
CAS
33252-32-3
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
118425
IUPAC Name
4-ethylpyridin-2-amine
InChI Key
SJWHILBZPGQBJE-UHFFFAOYSA-N
SMILES
CCC1=CC(=NC=C1)N

Description

2-Amino-4-ethylpyridine is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in developing drugs targeting neurological disorders.

Catalysis: It is used as a ligand in catalytic processes, enhancing reaction efficiency in organic synthesis, which is crucial for producing fine chemicals and pharmaceuticals.

Material Science: The compound is incorporated into polymer formulations to improve thermal stability and mechanical properties, making it valuable in the production of advanced materials.

Agricultural Chemicals: It plays a role in the formulation of agrochemicals, contributing to the development of more effective pesticides and herbicides, thereby supporting sustainable agriculture.

Analytical Chemistry: Utilized as a reagent in various analytical techniques, it aids in the detection and quantification of other substances, enhancing laboratory efficiency and accuracy.

References Data Source From Pubchem

Targeting ubiquitin specific proteases (USPs) in cancer immunotherapy: from basic research to preclinical application

Publication Name: Journal of experimental & clinical cancer research : CR
Publication Date: 2023-09-01
DOI: 10.1186/s13046-023-02805-y

N-Oxidation of Pyridines

Publication Name: Science of Synthesis
Publication Date: 2016

“Virtual Fragment Linking”: An Approach To Identify Potent Binders from Low Affinity Fragment Hits

Publication Name: Journal of Medicinal Chemistry
Publication Date: 2008-03-22
DOI: 10.1021/jm701314u

The Chichibabin Reaction and Related Processes

Publication Name: Science of Synthesis
Publication Date: 2006

2-Aminopyridines as Highly Selective Inducible Nitric Oxide Synthase Inhibitors. Differential Binding Modes Dependent on Nitrogen Substitution

Publication Name: Journal of Medicinal Chemistry
Publication Date: 2004-05-07
DOI: 10.1021/jm031035n