5766-79-0

Basic information

• Product Name: 2-PHENYL-2-PIPERIDINOACETONITRILE
• Synonyms: LABOTEST-BB LT00454898;2-PHENYL-2-PIPERIDINOACETONITRILE;1-(1-Cyanobenzyl)piperidine;1-(a-Cyanobenzyl)-piperidine;2-phenyl-2-piperidino-acetonitril;Acetonitrile, 2-phenyl-2-piperidino-;alpha-(1-Piperidyl)-alpha-tolunitrile;alpha-phenyl-1-piperidineacetonitril
• CAS NO: 5766-79-0
• Molecular Formula: C₁₃H₁₆N₂
• Molecular Weight: 200.28
• EINECS: 227-291-9
• Mol File: 5766-79-0.mol
• Article Data: 37

Chemical Properties

• Melting Point: 62 °C
• Boiling Point: 296.1°Cat760mmHg
• Flash Point: 118.1°C
• Appearance: /
• Density: 1.074g/cm³
• Vapor Pressure: 0.00147mmHg at 25°C
• Refractive Index: 1.56
• CAS DataBase Reference: 2-PHENYL-2-PIPERIDINOACETONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHENYL-2-PIPERIDINOACETONITRILE(5766-79-0)
• EPA Substance Registry System: 2-PHENYL-2-PIPERIDINOACETONITRILE(5766-79-0)

Safety Data

• Hazardous Substances Data: 5766-79-0(Hazardous Substances Data)

Usage

Uses

Phenylpiperidinoacetonitrile, is a building block used in various chemical synthesis.

InChI:InChI=1/C13H16N2/c14-11-13(12-7-3-1-4-8-12)15-9-5-2-6-10-15/h1,3-4,7-8,13H,2,5-6,9-10H2

Upstream product

• 110-89-4 piperidine 
• 100-52-7 benzaldehyde 
• 78-67-1 2,2'-azobis(isobutyronitrile) 
• 2905-56-8 N-Benzylpiperidine 
• 2591-86-8 N-Formylpiperidine 
• 7677-24-9 trimethylsilyl cyanide 
• 100-58-3 phenylmagnesium bromide 
• 108-88-3 toluene 
• 98-88-4 benzoyl chloride 
• 776-75-0 N-benzoylpiperidine 
• 3010-03-5 piperidin-1-yl-acetonitrile 
• 108-90-7 chlorobenzene 
• 532-28-5 (RS)-mandelonitrile 
• 75-86-5 2-hydroxy-2-methylpropanenitrile 

Downstream Products

• 107416-50-2 2-phenyl-2-(piperidin-1-yl)acetic acid hydrochloride 
• 72219-09-1 1-benzylpyrrolidine-2-carbonitrile 
• 1025-56-5 N-benzyl-2-phenyl-pyrrolidine 
• 1260380-74-2 1-benzyl-2-butylpyrrolidine 
• 14182-01-5 (2E)-2-methyl-1,3-diphenylprop-2-en-1-one 
• 7529-63-7 1-(1-phenylethyl)piperidine 
• 776-75-0 N-benzoylpiperidine 
• 7114-36-5 phenyl-piperidin-1-yl-acetaldehyde 
• 97295-28-8 2-Phenyl-2-piperidin-1-yl-malononitrile 
• 116858-54-9 C₂₆H₃₂N₂ 
• 123784-18-9 2-(piperidinobenzyl)pyridine 
• 116858-57-2 3-Ethoxy-2-phenyl-2-piperidin-1-yl-but-3-enenitrile 
• 116858-51-6 (Z)-2,3,5-Triphenyl-2,5-di-piperidin-1-yl-pent-4-enenitrile 
• 128407-28-3 (Z)-2,4-Diphenyl-2-piperidino-3-butenenitrile 

Relevant articles and documents

Electrochemically promoted oxidative α-cyanation of tertiary and secondary amines using cheap AIBN

The electrochemical α-cyanation of tertiary and secondary amines has been developed by using a cheap cyanide reagent, azobisisobutyronitrile (AIBN). The CN radical, generated throughn-Bu4NBr-meidated electrochemical oxidation, participates in a novel α-cyanation reaction under exogenous oxidant-free conditions.

A carbon dioxide-promoted three-component Strecker reaction

A three-component Strecker reaction of aldehydes, amines and KCN has been performed for the first time in supercritical carbon dioxide. In the proposed procedure, non-toxic and non-flammable carbon dioxide acts not only as an environmentally benign reaction medium but also as a reaction promoter via in situ formation of carbonic acid which provides a gradual release of the true cyanating agent (HCN) from available KCN. The reaction conditions (pressure, temperature, and concentrations of reagents) were optimized, and various aromatic and aliphatic amines and aldehydes were transformed into valuable α-amino nitriles including prospective pharmacological substances. The equimolar amount of used cyanogen reagent, carrying out the process in a sealed autoclave in a 'green' solvent medium under mild conditions (90 bar, 35 °C) along with the high yields of products and the scalability of the developed procedure make it suitable for sustainable industrial applications. This journal is

A unique combination of KI/ZnFe2O4 as a catalyst for oxidative Strecker reaction

α-Aminonitriles as key intermediates for the preparation of α-amino acid derivatives, amides, diamines, peptides, proteins and heterocycles were synthesized through methylarene oxidation in the Strecker reaction using a unique combination of KI/ZnFe2O4 as the best catalyst and aqueous tert-butyl hydroperoxide as oxidant. A wide range of amines and methylarenes were converted to the corresponding products. Operational simplicity, short reaction time and recyclability of the catalyst are advantages of this protocol.