5666-18-2

Basic information

• Product Name: 3,3-diphenylprop-2-en-1-amine
• Synonyms: 3,3-Diphenyl-2-propen-1-amine
• CAS NO: 5666-18-2
• Molecular Formula: C₁₅H₁₅N
• Molecular Weight: 209.2863
• Mol File: 5666-18-2.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 360°C at 760 mmHg
• Flash Point: 174.8°C
• Density: 1.043g/cm³
• Vapor Pressure: 2.29E-05mmHg at 25°C
• Refractive Index: 1.601
• CAS DataBase Reference: 3,3-diphenylprop-2-en-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3-diphenylprop-2-en-1-amine(5666-18-2)
• EPA Substance Registry System: 3,3-diphenylprop-2-en-1-amine(5666-18-2)

Safety Data

• Hazardous Substances Data: 5666-18-2(Hazardous Substances Data)

Upstream product

• 3531-24-6 3,3-diphenylacrylonitrile 
• 4320-44-9 3-hydroxy-3,3-diphenyl-propylamine 
• 119-61-9 benzophenone 
• 1061242-67-8 1-Aza-1,3-bis(triphenylphosphoranylidene)propane 
• 3531-23-5 3-hydroxy-3,3-diphenylpropanenitrile 
• 4801-14-3 3,3-diphenylprop-2-en-1-ol 
• 4801-15-4 3-bromo-1,1-diphenyl-1-propene 
• 108-86-1 bromobenzene 
• 3923-52-2 1,1-diphenyl-2-propyn-1-ol 

Downstream Products

• 138354-37-7 N-(3,3-diphenyl-2-propenyl)indole-2-carboxamide 
• 138354-45-7 Quinoline-2-carboxylic acid (3,3-diphenyl-allyl)-amide 
• 138354-46-8 Quinoline-3-carboxylic acid (3,3-diphenyl-allyl)-amide 
• 138384-12-0 Naphthalene-1-carboxylic acid (3,3-diphenyl-allyl)-amide 
• 138354-48-0 5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinoline-2-carboxylic acid (3,3-diphenyl-allyl)-amide 
• 138354-43-5 3,4-Dichloro-N-(3,3-diphenyl-allyl)-benzamide 
• 138354-40-2 N-(4-chlorophenyl)-N'-(3,3-diphenyl-2-propenyl)urea 
• 89482-39-3 N-benzoyl-3,3-diphenylprop-2-en-1-ylamine 
• 138354-47-9 Quinoline-4-carboxylic acid (3,3-diphenyl-allyl)-amide 
• 115129-81-2 N-benzoyl-N'-(3,3-diphenylprop-2-enyl)thiourea 
• 138354-42-4 4-Chloro-N-(3,3-diphenyl-allyl)-benzamide 
• 138354-44-6 Naphthalene-2-carboxylic acid (3,3-diphenyl-allyl)-amide 
• 112779-54-1 1,5-diphenyl-3H-2-benzazepine 
• 115129-87-8 N-(3,3-diphenylprop-2-enyl)thiourea 

Relevant articles and documents

Cascade reaction of propargylic alcohols with hydroxylamine hydrochloride: facile synthesis of α,β-unsaturated oximes and nitriles

We have developed an easy and practical method for the synthesis of α,β-unsaturated oximes and nitriles from readily available propargylic alcohols with hydroxylamine hydrochloride (NH2OH·HCl) under metal-free conditions. By using or not using p-toluenesulfonyl chloride (p-TsCl) as the dehydrating promoter, the desired nitriles or oximes could be obtained, respectively via a three-step one-pot or two-step one-pot process in moderate to excellent yields with good functional group compatibility.

A catalytic asymmetric chlorocyclization of unsaturated amides

The asymmetric chlorocyclization of unsaturated amides catalyzed by (DHQD)2PHAL yields oxazoline and dihydrooxazine derivatives (see scheme). The reaction is operationally simple and employs 1-2 mol % of the commercially available (DHQD)2PHAL (hydroquinidine 1,4-phthalazinediyl diether) catalyst. Different substitution patterns of the olefin as well as aromatic and aliphatic olefin substituents are well tolerated. DCDPH=N,N-dichloro-5,5-diphenylhydantoin. Copyright

Design and synthesis of N-(3,3-diphenylpropenyl)alkanamides as a novel class of high-affinity MT2-selective melatonin receptor ligands

A novel series of melatonin receptor ligands was discovered by opening the cyclic scaffolds of known classes of high affinity melatonin receptor antagonists, while retaining the pharmacophore elements postulated by previously described 3D-QSAR and recepto