782-87-6

Basic information

• Product Name: 3-[BENZYL-(2-CYANO-ETHYL)-AMINO]-PROPIONITRILE
• Synonyms: 3-[BENZYL-(2-CYANO-ETHYL)-AMINO]-PROPIONITRILE;3,3'-[(phenylmethyl)imino]bisPropanenitrile
• CAS NO: 782-87-6
• Molecular Formula: C₁₃H₁₅N₃
• Molecular Weight: 213.28
• Mol File: 782-87-6.mol
• Article Data: 21

Chemical Properties

• Boiling Point: 429.3 °C at 760 mmHg
• Flash Point: 195.3 °C
• Appearance: /
• Density: 1.072 g/cm³
• CAS DataBase Reference: 3-[BENZYL-(2-CYANO-ETHYL)-AMINO]-PROPIONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[BENZYL-(2-CYANO-ETHYL)-AMINO]-PROPIONITRILE(782-87-6)
• EPA Substance Registry System: 3-[BENZYL-(2-CYANO-ETHYL)-AMINO]-PROPIONITRILE(782-87-6)

Safety Data

• Hazardous Substances Data: 782-87-6(Hazardous Substances Data)

Usage

General Description

3-[Benzyl-(2-cyano-ethyl)-amino]-propionitrile is a chemical compound with the molecular formula C15H16N2. It is a propionitrile derivative that contains a benzyl group and a 2-cyano-ethyl-amino group. 3-[BENZYL-(2-CYANO-ETHYL)-AMINO]-PROPIONITRILE is used in organic synthesis and pharmaceutical research as a starting material for the preparation of various drugs and biologically active molecules. It is also used in the production of dyes, pigments, and other chemical intermediates. 3-[Benzyl-(2-cyano-ethyl)-amino]-propionitrile is considered a valuable building block in the chemical industry due to its versatility and potential applications in various fields.

Upstream product

• 107-13-1 acrylonitrile 
• 100-46-9 benzylamine 
• 706-03-6 3-(benzylamino)propionitrile 
• 111-94-4 3,3'-Iminodipropionitrile 
• 100-39-0 benzyl bromide 
• 620-05-3 iodomethylbenzene 
• 100-44-7 benzyl chloride 

Downstream Products

• 66128-33-4 N,N-bis(3-(N,N-bis(3-aminopropyl)amino)propyl)benzylamine 
• 66128-32-3 3-[[3-(benzyl-{3-[bis-(2-cyano-ethyl)-amino]-propyl}-amino)-propyl]-(2-cyano-ethyl)-amino]-propionitrile 
• 1030328-96-1 (±)-4-amino-1-benzylpiperidine-3-carbonitrile 
• 3518-88-5 3,3'-imino-di-propionic acid diethyl ester 
• 6938-07-4 N,N-bis(2-ethoxycarbonylethyl)benzylamine 
• 108442-14-4 9-benzyl-2-(3-fluorophenyl)-7,8,9,10-tetrahydropyrido[3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one 
• 116798-99-3 9-benzyl-2(2-chlorophenyl)-7,8,9,10-tetrahydropyrido[3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one 
• 108442-23-5 9-benzyl-2-(2-fluorophenyl)-7,8,9,10-tetrahydropyrido[3,4-e][1,2,4]triazolo [1,5-c]pyrimidin-5(6H)one 
• 116799-00-9 9-benzyl-2-(2-pyridyl)-7,8,9,10-tetrahydropyrido[3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one 
• 108461-24-1 9-benzyl-2-(4-chlorophenyl)-7,8,9,10-tetrahydropyrido [3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one 
• 108442-26-8 8-Benzyl-2-(4-fluoro-phenyl)-6,7,8,9-tetrahydro-5H-1,3,3a,5,8-pentaaza-cyclopenta[a]naphthalen-4-one 
• 135481-50-4 8-Benzyl-2-(1H-pyrrol-2-yl)-6,7,8,9-tetrahydro-5H-1,3,3a,5,8-pentaaza-cyclopenta[a]naphthalen-4-one 
• 108442-13-3 9-benzyl-2-phenyl-7,8,9,10-tetrahydropyrido[3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one 
• 135481-58-2 4-<<(2-fluorophenyl)methyl>amino>-5,6,7,8-tetrahydro-6-(phenylmethyl)pyrido<3,4-d>pyrimidin-2(1H)-one 

Relevant articles and documents

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Cultivation of a Cu/HMPC catalyst from a hyperaccumulating mustard plant for highly efficient and selective coupling reactions under mild conditions

Cu-containing activated carbon (eco-catalyst, Cu/HMPC, where 'C' defines 'carbon') was derived from a metal-hyperaccumulating mustard plant (HMP) by a simple chemical activation method. Transmission electron microscopy/selected area diffraction (HRTEM/SAED) results revealed that the Cu/HMPC has mainly three types of morphology [sheet-like morphology (2D), hollow-spheres (3D) and needle-like structures (1D)] which are interconnected. HRTEM-SAED, Raman and X-ray photoelectron spectroscopy (XPS) results confirmed the existence of Cu oxide species in Cu/HMPC. Content of Cu in Cu/HMPC was determined to be 1.03 wt%. The quality of graphitization in Cu/HMPC was discussed by using Raman and XRD results. The BET surface area of Cu/HMPC was determined to be 620.8 m2 g-1. The Cu/HMPC actively transformed a wide range of amines to imines under very mild reaction conditions. The catalyst Cu/HMPC gave products in excellent yields (98-61%) with very high TON/TOF values (1512/339-833/35 h-1). To the best of our knowledge, this is the most efficient Cu-based heterogeneous eco-catalyst for the synthesis of imines among those reported to date. The Cu can be recovered from used Cu/HMPC by a simple HCl treatment. Versatility, heterogeneity and reusability of Cu/HMPC were tested. A possible mechanism has been proposed.

Convergent synthesis of polynitrile and/or polyamine dendrimers through hydroaminomethylation and Michael addition

A general concept for a versatile convergent synthesis ofpolynitrile and/or polyamine dendrimers has been developed by applying Voegtle's procedure in combination with thetandem hydroformylation/reductive amination sequence, known as hydroaminomethylation