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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

Application

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

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