1334158-43-8

Basic information

• Product Name: (E)-3,4-diphenylbut-3-en-1-ol
• Synonyms: (E)-3,4-diphenylbut-3-en-1-ol
• CAS NO: 1334158-43-8
• Molecular Weight: 224.302
• Mol File: 1334158-43-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (E)-3,4-diphenylbut-3-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3,4-diphenylbut-3-en-1-ol(1334158-43-8)
• EPA Substance Registry System: (E)-3,4-diphenylbut-3-en-1-ol(1334158-43-8)

Safety Data

• Hazardous Substances Data: 1334158-43-8(Hazardous Substances Data)

Upstream product

• 451-40-1 phenyl benzyl ketone 
• 1332458-92-0 2-benzyl-2-phenyloxetane 
• 22927-23-7 4-phenyl-2,3-dihydrofuran 
• 100-58-3 phenylmagnesium bromide 
• 10229-11-5 4-phenyl-but-3-yn-1-ol 
• 98-80-6 phenylboronic acid 
• 591-50-4 iodobenzene 

Downstream Products

• 7694-30-6 cis-1,2-diphenylcyclobutane 
• 67966-93-2 (1-benzylcyclopropyl)benzene 

Relevant articles and documents

Catalytic Regioselective Isomerization of 2,2-Disubstituted Oxetanes to Homoallylic Alcohols

The selective isomerization of strained heterocyclic compounds is an important tool in organic synthesis. An unprecedented regioselective isomerization of 2,2-disubstituted oxetanes into homoallylic alcohols is described. The use of tris(pentafluorophenyl

Ni-catalyzed stereoselective arylation of inert C-O bonds at low temperatures

A Ni-catalyzed arylation of inert C-O bonds that operates at temperatures as low as -40 C is described. Unlike other methods for C-O bond cleavage utilizing organometallic species, this protocol operates at low temperatures, thus allowing the presence of sensitive functional groups with exquisite site-selectivity and stereoselectivity.