1488-20-6

Basic information

• Product Name: 3-[(2-phenylethyl)amino]propanenitrile
• Synonyms: 3-[(2-phenylethyl)amino]propanenitrile
• CAS NO: 1488-20-6
• Molecular Formula: C₁₁H₁₄N₂
• Molecular Weight: 174
• Mol File: 1488-20-6.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 3-[(2-phenylethyl)amino]propanenitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[(2-phenylethyl)amino]propanenitrile(1488-20-6)
• EPA Substance Registry System: 3-[(2-phenylethyl)amino]propanenitrile(1488-20-6)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 1488-20-6(Hazardous Substances Data)

Usage

General Description

3-[(2-phenylethyl)amino]propanenitrile is a chemical compound with the molecular formula C11H13N. It is a nitrile compound that contains a phenethylamine moiety, with a nitrile group attached to the third carbon of the propane chain. 3-[(2-phenylethyl)amino]propanenitrile is often used in pharmaceutical and research settings, where it may be utilized for its potential as an intermediate in the synthesis of various organic compounds. Additionally, 3-[(2-phenylethyl)amino]propanenitrile may have potential applications in medicinal chemistry due to its structural similarities to other biologically active compounds. However, as with any chemical compound, proper handling and safety precautions should be observed when working with this substance.

Upstream product

• 64-04-0 phenethylamine 
• 107-13-1 acrylonitrile 

Downstream Products

• 3936-51-4 N-(2-phenylethyl)-1,3-propanediamine 

Relevant articles and documents

Cadmium chloride (CdCl2): An efficient catalyst for conjugate addition of amines to electron-poor alkenes

Electron-deficient olefins undergo rapid Aza-Michael reaction with a wide range of amines catalyzed by cadmium chloride at room temperature. Copyright Taylor & Francis Group, LLC.

Ruthenium (II) β-diketimine as hydroamination catalyst, crystal structure and DFT computations

A new half-sandwich ruthenium (II) complex containing β-diketiminate ligand has been synthesized and used for hydroamination of acrylonitrile with aromatic and aliphatic amines. The catalytic activity of prepared complex was compared with a series of ruthenium complexes of β-diketiminate ligands, and the effect of electronic and steric properties of these ligands on catalytic activity of their complexes was investigated. Replacement of H atom in α position of β-diketiminate with (CF3) as an electron-withdrawing group leads to decreasing the reaction yield, and on the other hand, electron-donating group (CH3) has the opposite effect. In addition, crystal structure of [Ru(p-cymen)Cl(LH,Cl)] was determined by single X-ray crystallography. Hirshfeld surface analysis has been performed to determine the dominate interactions in molecular crystal. Furthermore, density functional, QTAIM and energy calculations have been carried out, to get the detailed insight into electronic and bonding characteristics of titled compound.

Aminocarbonyl-substituted benzimidazoles having tryptase-inhibitory activity

A method for treating diseases in which tryptase inhibitors may be of thereapeutic value, which comprises the administration of a thereapeutic amount of a compound of the formula ? The invention also comprises novel compounds of the formula (I). Exemplary is 2-[2-(4-amidinophenyl)ethyl]-1-methyl-benzimidazol-5-yl-carboxylic acid-N-(pyridin-3-yl-methyl)-N-methyl-amide-hydrochloride.