137642-06-9

Basic information

• Product Name: (N-phenyl)-1-(pyridin-3-yl)ethanamine
• Synonyms: (N-phenyl)-1-(pyridin-3-yl)ethanamine;(S)-1-(pyridin-3-yl)ethanaMine;3-PyridineMethanaMine, a-Methyl-N-phenyl-
• CAS NO: 137642-06-9
• Molecular Formula: C13H14N2
• Molecular Weight: 198.27
• Mol File: 137642-06-9.mol

Chemical Properties

• Boiling Point: 341.2±17.0 °C(Predicted)
• Appearance: /
• Density: 1.101±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 5.63±0.11(Predicted)
• CAS DataBase Reference: (N-phenyl)-1-(pyridin-3-yl)ethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: (N-phenyl)-1-(pyridin-3-yl)ethanamine(137642-06-9)
• EPA Substance Registry System: (N-phenyl)-1-(pyridin-3-yl)ethanamine(137642-06-9)

Safety Data

• Hazardous Substances Data: 137642-06-9(Hazardous Substances Data)

Usage

Uses

(N-phenyl)-1-(pyridin-3-yl)ethanamine is used as a chemical intermediate in the synthesis of various organic compounds. Its unique structure, which includes both a phenyl and a pyridin-3-yl group, allows it to be a versatile building block for the creation of more complex molecules. Although it does not have many common applications related to its nature and properties, its potential use in the development of new compounds and materials is significant. This makes it a valuable compound for researchers and chemists working in the field of organic chemistry and related industries.

Upstream product

• 1121-55-7 3-vinylpyridine 
• 62-53-3 aniline 

Relevant articles and documents

Structural models of vanadate-dependent haloperoxidases, their reactivity, immobilization on polymer support and catalytic activities

The design of structural and functional models of enzymes vanadate-dependent haloperoxidases (VHPO) and the isolation and/or generation of species having {VO(H2O)}, {VO2}, {VO(OH)} and {VO(O 2)} cores, proposed as intermediate(s) during catalytic action, in solution have been studied. Catalytic potential of these complexes have been tested for oxo-transfer as well as oxidative bromination and sulfide oxidation reactions. Some of the oxidovanadium(IV) and dioxidovanadium(V) complexes have been immobilized on polymer support in order to improve their recycle ability during catalytic activities and turn over number. The formulations of the polymer-anchored complexes are based on the respective neat complexes and conclusions drawn from the various characterization studies. These catalysts have successfully been used for all catalytic reactions mentioned above. These catalysts are stable and recyclable. Indian Academy of Sciences.