3,4-Dibromo-1-oxo-1,3-diphenylbutan-2-yl benzoate

Base Information

Chemical Name:3,4-Dibromo-1-oxo-1,3-diphenylbutan-2-yl benzoate
CAS No.:7472-85-7
Molecular Formula:C₂₃H₁₈Br₂O₃
Molecular Weight:502.202
Hs Code.:
NSC Number:402000
DSSTox Substance ID:DTXSID20331227

Synonyms:7472-85-7;NSC402000;DTXSID20331227;NSC-402000;3,4-Dibromo-1-oxo-1,3-diphenylbutan-2-yl benzoate

Suppliers and Price of 3,4-Dibromo-1-oxo-1,3-diphenylbutan-2-yl benzoate

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 5 raw suppliers

Chemical Property of 3,4-Dibromo-1-oxo-1,3-diphenylbutan-2-yl benzoate

Chemical Property:

Vapor Pressure:5.32E-15mmHg at 25°C
Boiling Point:613.8°Cat760mmHg
Flash Point:325°C
Density:1.547g/cm³
XLogP3:6.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:8
Exact Mass:501.96022
Heavy Atom Count:28
Complexity:520

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)C(C(CBr)(C2=CC=CC=C2)Br)OC(=O)C3=CC=CC=C3

Technology Process of 3,4-Dibromo-1-oxo-1,3-diphenylbutan-2-yl benzoate

There total 2 articles about 3,4-Dibromo-1-oxo-1,3-diphenylbutan-2-yl benzoate 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:

: 19513-91-8,23265-28-3,23265-29-4,70292-05-6,138451-21-5,138451-22-6
(E)-4-bromo-2,3-epoxy-1,3-diphenyl-1-butanone

: 7472-85-7
(2RS,3SR)-2-benzoyloxy-3,4-dibromo-1,3-diphenyl-butan-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether; HBr

With diethyl ether; hydrogen bromide;
DOI:10.1021/jo01083a010