3597-67-9

Basic information

• Product Name: 2-amino-3,3-diphenylcyclopent-1-ene-1-carbonitrile
• CAS NO: 3597-67-9
• Molecular Formula: C₁₈H₁₆N₂
• Molecular Weight: 260.333
• Mol File: 3597-67-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 483.5°C at 760 mmHg
• Flash Point: 246.2°C
• Density: 1.17g/cm³
• Vapor Pressure: 1.66E-09mmHg at 25°C
• Refractive Index: 1.647
• CAS DataBase Reference: 2-amino-3,3-diphenylcyclopent-1-ene-1-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-3,3-diphenylcyclopent-1-ene-1-carbonitrile(3597-67-9)
• EPA Substance Registry System: 2-amino-3,3-diphenylcyclopent-1-ene-1-carbonitrile(3597-67-9)

Safety Data

• Hazardous Substances Data: 3597-67-9(Hazardous Substances Data)

Usage

Chemical compound

2-amino-3,3-diphenylcyclopent-1-ene-1-carbonitrile

Molecular structure

Contains an amino group, two phenyl groups, a carbonitrile group, and a cyclopentene ring

Potential applications

Medicinal chemistry and organic synthesis

Need for further research

To fully understand potential uses and effects

Upstream product

• 6727-73-7 4-iodobutyronitrile 
• 86-29-3 Diphenylacetonitrile 
• 5332-06-9 4-bromobutanenitrile 
• 15144-62-4 2,2-diphenylhexane-1,6-dinitrile 

Downstream Products

• 1353573-88-2 5-{[4-(2-methoxyphenyl)piperazin-1-yl]methyl}-2,2-diphenylcyclopentan-1-one oxalate 
• 1353573-85-9 5-({[2-(2-methoxyphenoxy)ethyl]amino}methyl)-2,2-diphenylcyclopentan-1-one oxalate 
• 1353573-77-9 5-({[2-(2-methoxyphenoxy)ethyl]amino}methyl)-2,2-diphenylcyclopentan-1-one 
• 1353573-81-5 5-{[(2-phenoxyethyl)amino]methyl}-2,2-diphenylcyclopentan-1-one oxalate 
• 1353573-75-7 5-{[(2-phenoxyethyl)amino]methyl}-2,2-diphenylcyclopentan-1-one 
• 111357-61-0 2,2-diphenyl-adipic acid-1-methyl ester 
• 112116-43-5 2,2-diphenyl-adipic acid dimethyl ester 
• 15324-42-2 2,2-diphenylcyclopentanone 

Relevant articles and documents

Synthesis, biological evaluation, and docking studies of tetrahydrofuran-cyclopentanone-and cyclopentanol-based ligands acting at adrenergic α1- and serotonine 5-HT1A receptors

A series of aralkylphenoxyethylamine and aralkylmethoxyphenylpiperazine compounds was synthesized and their in vitro pharmacological profile at both 5-HT1A receptors and α1-adrenoceptor subtypes was measured by binding assay and func

Nitroalkene Inter /Intra Tandem Cycloadditions. 7. Application of (R)-(-)-2,2-Diphenylcyclopentanol as the Chiral Auxiliary

Chiral enol ethers derived from (R)-(-)-2,2-diphenylcyclopentanol ((-)3) have been found to provide high levels of asymmetric induction in tandem inter /intra nitroalkene cycloadditions.The chiral auxiliary (>97percent ee) is readily prepar