1,1'-(2-Bromobuta-1,3-diene-1,1-diyl)dibenzene

Base Information

Chemical Name:1,1'-(2-Bromobuta-1,3-diene-1,1-diyl)dibenzene
CAS No.:51752-41-1
Molecular Formula:C₁₆H₁₃Br
Molecular Weight:285.183
Hs Code.:
DSSTox Substance ID:DTXSID80522316
Mol file:51752-41-1.mol

Synonyms:51752-41-1;1,1'-(2-Bromobuta-1,3-diene-1,1-diyl)dibenzene;DTXSID80522316

Suppliers and Price of 1,1'-(2-Bromobuta-1,3-diene-1,1-diyl)dibenzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1,1'-(2-Bromobuta-1,3-diene-1,1-diyl)dibenzene

Chemical Property:

XLogP3:5.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:3
Exact Mass:284.02006
Heavy Atom Count:17
Complexity:258

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C=CC(=C(C1=CC=CC=C1)C2=CC=CC=C2)Br

Technology Process of 1,1'-(2-Bromobuta-1,3-diene-1,1-diyl)dibenzene

There total 3 articles about 1,1'-(2-Bromobuta-1,3-diene-1,1-diyl)dibenzene 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: 62.0%

: 30979-49-8
1,1-dibromo-2,2-diphenyl-3-methylcyclopropane

: 51752-41-1
1,1-Diphenyl-2-bromo-1,3-butadien

Guidance literature:: With quinoline; at 130 - 140 ℃;

Reference yield:

: 51752-40-0
2,4-dibromo-1,1-diphenylbut-1-ene

: 51752-41-1
1,1-Diphenyl-2-bromo-1,3-butadien

Guidance literature:: With potassium hydroxide; In methanol; Ambient temperature;

Reference yield:

: 7632-57-7
diphenylmethylenecyclopropene

: 51752-41-1
1,1-Diphenyl-2-bromo-1,3-butadien

Guidance literature:: Multi-step reaction with 2 steps

1: Br₂ / CH₂Cl₂

2: KOH / methanol / Ambient temperature

With potassium hydroxide; bromine; In methanol; dichloromethane;