62071-27-6

Basic information

• Product Name: 5-oxo-2,3,5-triphenylpentanenitrile
• Synonyms: gamma-Benzoyl-alpha,beta-diphenylbutyronitrile
• CAS NO: 62071-27-6
• Molecular Formula: C₂₃H₁₉NO
• Molecular Weight: 325.4031
• Mol File: 62071-27-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 522.1°C at 760 mmHg
• Flash Point: 269.5°C
• Density: 1.134g/cm³
• Vapor Pressure: 5.36E-11mmHg at 25°C
• Refractive Index: 1.607
• CAS DataBase Reference: 5-oxo-2,3,5-triphenylpentanenitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 5-oxo-2,3,5-triphenylpentanenitrile(62071-27-6)
• EPA Substance Registry System: 5-oxo-2,3,5-triphenylpentanenitrile(62071-27-6)

Safety Data

• Hazardous Substances Data: 62071-27-6(Hazardous Substances Data)

Upstream product

• 140-29-4 phenylacetonitrile 
• 94-41-7 benzalacetophenone 
• 614-47-1 1,3-diphenyl-propen-3-one 

Downstream Products

• 854446-22-3 3-benzoyl-4-oxo-1,2,6-triphenyl-cyclohexanecarbonitrile 
• 3298-21-3 5-Oximino-2,3,5-triphenyl-pentansaeure-amid 
• 3298-26-8 5-Oximino-2,3,5-triphenyl-pentansaeure-hydroxyimidat 
• 502187-52-2 2-bromo-3,4,6-triphenyl-pyridine 
• 70028-35-2 3,4,6-triphenyl-3,4-dihydro-1H-pyridin-2-one 
• 95812-77-4 2-bromo-5-oxo-2,3,5-triphenyl-valeronitrile 
• 6323-01-9 5-oxo-2-(3-oxo-1,3-diphenyl-propyl)-2,3,5-triphenyl-valeronitrile 
• 872272-73-6 2,4,5-triphenyl-piperidine 
• 6341-61-3 4-oxo-1,2,6-triphenyl-cyclohexanecarbonitrile 
• 58305-72-9 3,5-dibenzyliden-4-oxo-1,2,6-triphenyl-cyclohexanecarbonitrile 

Relevant articles and documents

Access to 2-Amino-3-Arylthiophenes by Base-Catalyzed Redox Condensation Reaction Between Arylacetonitriles, Chalcones, and Elemental Sulfur

A straightforward access to 2-amino-3-arylthiophenes has been developed via one-pot two-step three-component reaction of arylacetonitriles, chalcones and elemental sulfur. The first step consists of a DBU-catalyzed formation of Michael adduct between aryl

Water-soluble calixarenes as new inverse phase-transfer catalysts. Their application to aldol-type condensation and Michael addition reactions in water

Aldol-type condensation and Michael addition reactions of activated methyl and methylene compounds in aqueous NaOH solution have been developed without the need for any added organic solvents. The water-soluble calix[n]arenes, which contain trimethylammon

CONJUGATE ADDITION IN PHASE TRANSFER CATALYSIS CONDITIONS: REACTIONS OF α ENONES WITH ARYLACETONITRILES

Conjugate addition of arylacetonitriles 1-3 to α-enones 4-6 can be performed in liquid-liquid PTC conditions (toluene-saturated aqueous K2CO3 solution).The reaction is too slow with isophorone or mesityloxide to be synthetically useful.