Phenol, 4-(2-bromo-1,2-diphenylethenyl)-, (Z)-

Base Information

• Chemical Name: Phenol, 4-(2-bromo-1,2-diphenylethenyl)-, (Z)-
• CAS No.: 61923-53-3
• Molecular Formula: C20H15BrO
• Molecular Weight: 351.2365
• Mol file: 61923-53-3.mol

Synonyms:Phenol, 4-(2-bromo-1,2-diphenylethenyl)-, (Z)-;(E,Z)-1-BROMO-1,2-DIPHENYL-2-(4-HYDROXYPHENYL)ETHENE;(Z)-4-(2-Bromo-1,2-diphenylethenyl)phenol;61923-53-3;874504-11-7;C20-H15-Br-O

Chemical Property of Phenol, 4-(2-bromo-1,2-diphenylethenyl)-, (Z)-

Chemical Property:

• Vapor Pressure: 2.59E-08mmHg at 25°C
• Boiling Point: 438.9°Cat760mmHg
• Flash Point: 219.2°C
• Density: 1.382g/cm³
• XLogP3: 6.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 350.03063
• Heavy Atom Count: 22
• Complexity: 369

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(=C(C2=CC=CC=C2)Br)C3=CC=C(C=C3)O
• Isomeric SMILES: C1=CC=C(C=C1)/C(=C(\C2=CC=CC=C2)/Br)/C3=CC=C(C=C3)O

Technology Process of Phenol, 4-(2-bromo-1,2-diphenylethenyl)-, (Z)-

There total 4 articles about Phenol, 4-(2-bromo-1,2-diphenylethenyl)-, (Z)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

(+/-)-[1-(4-hydroxyphenyl)]-1,2-diphenylethanol (355803-76-8) → E,Z-1-bromo-1,2-diphenyl-2-(4-hydroxyphenyl)ethene (61923-53-3,97151-00-3)

Guidance literature:

With tetrachloromethane; bromine;

Reference yield:

4-Hydroxybenzophenone (1137-42-4) → E,Z-1-bromo-1,2-diphenyl-2-(4-hydroxyphenyl)ethene (61923-53-3,97151-00-3)

Guidance literature:

Multi-step reaction with 2 steps

1: diethyl ether

2: tetrachloromethane; bromine

With tetrachloromethane; diethyl ether; bromine;

Reference yield:

benzylmagnesium chloride (6921-34-2) → E,Z-1-bromo-1,2-diphenyl-2-(4-hydroxyphenyl)ethene (61923-53-3,97151-00-3)

Guidance literature:

Multi-step reaction with 2 steps

1: diethyl ether

2: tetrachloromethane; bromine

With tetrachloromethane; diethyl ether; bromine;

upstream raw materials:

(+/-)-[1-(4-hydroxyphenyl)]-1,2-diphenylethanol

tetrachloromethane

bromine

4-Hydroxybenzophenone

Downstream raw materials:

trans-(E)-1-bromo-2-<4-<2-(dimethylamino)ethoxy>phenyl>-1,2-diphenylethene

cis-(Z)-1-bromo-2-<4-<2-(dimethylamino)ethoxy>phenyl>-1,2-diphenylethene

(E/Z)-1-bromo-2-(p-methoxyphenyl)-1,2-diphenylethene

E,Z-1-<4-<2-(dimethylamino)ethoxy>phenyl>-1,2-diphenylethene