5-(Bromomethyl)-3-phenyl-1,3-oxazolidin-2-one

Base Information

Chemical Name:5-(Bromomethyl)-3-phenyl-1,3-oxazolidin-2-one
CAS No.:98963-12-3
Molecular Formula:C10H10BrNO2
Molecular Weight:256.099
Hs Code.:2934999090
Mol file:98963-12-3.mol

Synonyms:KE-0706;5-(bromomethyl)-3-phenyloxazolidin-2-one;bromomethylphenyloxazolidinone;

Suppliers and Price of 5-(Bromomethyl)-3-phenyl-1,3-oxazolidin-2-one

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

Matrix Scientific
5-(Bromomethyl)-3-phenyl-1,3-oxazolidin-2-one >95%
1g
$ 228.00

Matrix Scientific
5-(Bromomethyl)-3-phenyl-1,3-oxazolidin-2-one >95%
500mg
$ 181.00

Crysdot
5-(Bromomethyl)-3-phenyloxazolidin-2-one 95+%
5g
$ 425.00

AK Scientific
5-(Bromomethyl)-3-phenyl-1,3-oxazolidin-2-one
100mg
$ 197.00

Total 7 raw suppliers

Chemical Property of 5-(Bromomethyl)-3-phenyl-1,3-oxazolidin-2-one

Chemical Property:

PSA：29.54000
LogP:2.47170

Purity/Quality:

97% ^*data from raw suppliers

5-(Bromomethyl)-3-phenyl-1,3-oxazolidin-2-one >95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 5-(Bromomethyl)-3-phenyl-1,3-oxazolidin-2-one

There total 2 articles about 5-(Bromomethyl)-3-phenyl-1,3-oxazolidin-2-one 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: 99.0%

: 169268-95-5
tert-butyl allyl(phenyl)carbamate

: 98963-12-3
5-(bromomethyl)-3-phenyloxazolidin-2-one

Guidance literature:: With N-Bromosuccinimide; In acetonitrile; at 20 ℃; for 24h; Reagent/catalyst; Solvent; Time; chemoselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2017.04.063