4-(1-Bromoethyl)benzophenone

Base Information

Chemical Name:4-(1-Bromoethyl)benzophenone
CAS No.:79316-80-6
Molecular Formula:C15H13BrO
Molecular Weight:289.172
Hs Code.:
DSSTox Substance ID:DTXSID60451438
Nikkaji Number:J1.942.390E

Synonyms:4-(1-Bromoethyl)benzophenone;79316-80-6;AGN-PC-0NE7YO;SCHEMBL677887;DTXSID60451438

Suppliers and Price of 4-(1-Bromoethyl)benzophenone

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of 4-(1-Bromoethyl)benzophenone

Chemical Property:

XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:288.01498
Heavy Atom Count:17
Complexity:250

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 4-(1-Bromoethyl)benzophenone

There total 4 articles about 4-(1-Bromoethyl)benzophenone 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: 82.0%

: 18220-90-1
4-ethylbenzophenone

: 79316-80-6
[4-(1-bromoethyl)phenyl](phenyl)methanone

Guidance literature:: With N-Bromosuccinimide; In tetrachloromethane; Heating;
DOI:10.1081/SCC-120023419

Reference yield:

: 100-41-4,27536-89-6
ethylbenzene

: 79316-80-6
[4-(1-bromoethyl)phenyl](phenyl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / AlCl₃ / CH₂Cl₂ / 4 h / 0 - 30 °C

2: 82 percent / N-bromosuccinimide / CCl₄ / Heating

With N-Bromosuccinimide; aluminium trichloride; In tetrachloromethane; dichloromethane; 1: Friedel-Crafts benzoylation;
DOI:10.1081/SCC-120023419

Reference yield:

: 98-88-4
benzoyl chloride

: 79316-80-6
[4-(1-bromoethyl)phenyl](phenyl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / AlCl₃ / CH₂Cl₂ / 4 h / 0 - 30 °C

2: 82 percent / N-bromosuccinimide / CCl₄ / Heating

With N-Bromosuccinimide; aluminium trichloride; In tetrachloromethane; dichloromethane; 1: Friedel-Crafts benzoylation;
DOI:10.1081/SCC-120023419