50485-27-3

Basic information

• Product Name: 2-benzyl-1,3-diphenyl-1-propene
• Synonyms: 2-benzyl-1,3-diphenyl-1-propene
• CAS NO: 50485-27-3
• Molecular Weight: 284.401
• Mol File: 50485-27-3.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 2-benzyl-1,3-diphenyl-1-propene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzyl-1,3-diphenyl-1-propene(50485-27-3)
• EPA Substance Registry System: 2-benzyl-1,3-diphenyl-1-propene(50485-27-3)

Safety Data

• Hazardous Substances Data: 50485-27-3(Hazardous Substances Data)

Upstream product

• 6712-97-6 tribenzylcarbinol 
• 75-36-5 acetyl chloride 
• 1449-46-3 benzyltriphenylphosphonium bromide 
• 102-04-5 1,3-Diphenylpropanone 
• 110-05-4 di-tert-butyl peroxide 
• 3582-84-1 (2-phenylethyl)diphenylphosphine oxide 
• 100-39-0 benzyl bromide 
• 100-52-7 benzaldehyde 
• 6921-34-2 benzylmagnesium chloride 
• 101-97-3 Ethyl 2-phenylethanoate 
• 124992-97-8 2-(1,3-diphenylpropyl) phenyl sulfone 
• 3112-85-4 methylphenylsulfonate 
• 925-90-6 ethylmagnesium bromide 
• 4742-03-4 2-benzyl-2-bromo-1,3-diphenyl-propane 

Downstream Products

• 6624-04-0 2-benzyl-1,3-diphenyl-propan-1-one 
• 24547-82-8 2-benzyl-1,3-diphenylpropan-1-ol 
• 4742-04-5 2-benzyl-1,3-diphenyl-propane 
• 719282-85-6 (C₆H₅CHSn(C₆H₅)3)2CCHC₆H₅ 
• 24547-83-9 2,4-Diphenyl-3-benzyl-butyraldehyd 
• 24547-84-0 2,4-Diphenyl-3-benzyl-1-butanol 
• 24547-85-1 2,4-Diphenyl-3-benzyl-1-buten 

Relevant articles and documents

NOVEL VINYLBENZENE COMPOUND AND PHOTOSENSITIVE PHOTORESIST COMPOSITION COMPRISING THE SAME

Provided is a photocurable composition comprising: (A) a photocurable compound; and (B) a vinylbenzene-containing monomer having a structure represented by chemical formula 1. In the chemical formula 1, X, R1, R2, R3, L, L1, L2 and L3 are the same as defi

Modern Friedel-Crafts chemistry. Part-29. Cyclialkylation of some triphenylated propane, butane and pentane substrates to diphenylated indans under Friedel-Crafts conditions

Reactions under Friedel-Crafts cyclialkylation conditions produced : isomeric 1,2-diphenylindans from 1,2,3-triphenyl-(1- or 2-)propanol and 1-chloro-2,3,3-triphenylpropane, trans-2-benzyl-1-phenylindan from 2-benzyl-1,3-diphenyl-2-propanol, isomeric 1-me

Alkene synthesis: Elimination of arenesulfinic acid from alkyl aryl sulfones using potassium trimethylsilanolate as base

The use of potassium trimethylsilanolate as base to induce elimination of potassium arenesulfinate from alkyl aryl sulfones to produce E-alkenes is described. The reaction was appropriate for substrates containing a benzyl or allyl group α to the sulfone