14377-99-2

Basic information

• Product Name: 1,2,3-triphenyl-1,3-propanedicarbonitrile
• Synonyms: 1,2,3-triphenyl-1,3-propanedicarbonitrile
• CAS NO: 14377-99-2
• Molecular Weight: 322.409
• Mol File: 14377-99-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2,3-triphenyl-1,3-propanedicarbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3-triphenyl-1,3-propanedicarbonitrile(14377-99-2)
• EPA Substance Registry System: 1,2,3-triphenyl-1,3-propanedicarbonitrile(14377-99-2)

Safety Data

• Hazardous Substances Data: 14377-99-2(Hazardous Substances Data)

Upstream product

• 6114-57-4 (Z)-2,3-diphenylacrylonitrile 
• 100-47-0 benzonitrile 
• 140-29-4 phenylacetonitrile 
• 100-52-7 benzaldehyde 

Downstream Products

• 127679-78-1 methyl (2S,4R)-2,3,4-triphenylpentanedioate 
• 127680-16-4 5-(4-methoxy-1-naphthyl)-5-oxo-2,3,4-triphenylpentanoic acid 
• 127680-14-2 5-(3,4-dimethoxyphenyl)-5-oxo-2,3,4-triphenylpentanoic acid 
• 127680-15-3 5-(4-ethoxyphenyl)-5-oxo-2,3,4-triphenylpentanoic acid 
• 127680-11-9 ((1R,2R)-3-Oxo-2-phenyl-indan-1-yl)-phenyl-acetic acid methyl ester 
• 127680-10-8 2,3-dihydro-1-oxo-2,α-diphenyl-1H-indene-3-acetic acid 
• 127680-09-5 2,3,4-triphenylpentanedioic anhydride 
• 127680-08-4 (2S,4R) 2,3,4-triphenylpentanedioic acid 
• 127680-09-5 2,3,4-triphenyl-glutaric acid-anhydride 
• 74-90-8 hydrogen cyanide 
• 64-04-0 phenethylamine 
• 103-29-7 1,1'-(1,2-ethanediyl)bisbenzene 
• 127680-08-4 2,3,4-triphenyl-glutaric acid 
• 16610-80-3 (E)-2,3-diphenylacrylonitrile 

Relevant articles and documents

Solvent-free condensation of arylacetonitrile with aldehydes

The condensation of a series of arylacetonitriles with aldehydes can be carried out by mixing equivalent amounts of reagents with neat powdered KOH at room temperature for 3-60 min depending on the aldehyde steric hindrance. At higher temperature (110°C), yields were generally higher and purity increased within very short reaction times (1-5 min). With pentamethylphenylacetonitrile, a phase transfer agent was necessary to give a satisfactory yield.

Studies in Friedel-Crafts reaction: Part V - Preparation and the Friedel-Crafts reaction of 2,3,4-triphenylpentanedioic anhydride

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