2-Oxazolidinone, 3-cyclohexyl-5-phenyl-

Base Information

Chemical Name:2-Oxazolidinone, 3-cyclohexyl-5-phenyl-
CAS No.:56805-21-1
Molecular Formula:C15H19NO2
Molecular Weight:245.321
Hs Code.:
DSSTox Substance ID:DTXSID40340997
Nikkaji Number:J117.088K
Mol file:56805-21-1.mol

Synonyms:2-Oxazolidinone, 3-cyclohexyl-5-phenyl-;56805-21-1;3-Cyclohexyl-5-phenyl-1,3-oxazolidin-2-one;DTXSID40340997;3-cyclohexyl-5-phenyloxazolidin-2-one;3-Cyclohexyl-5-phenyl-2-oxazolidinone;3-Cyclohexyl-5-phenyl-1,3-oxazolidin-2-one #

Suppliers and Price of 2-Oxazolidinone, 3-cyclohexyl-5-phenyl-

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 2-Oxazolidinone, 3-cyclohexyl-5-phenyl-

Chemical Property:

PSA：29.54000
LogP:3.45050
XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:245.141578849
Heavy Atom Count:18
Complexity:293

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(CC1)N2CC(OC2=O)C3=CC=CC=C3

Technology Process of 2-Oxazolidinone, 3-cyclohexyl-5-phenyl-

There total 8 articles about 2-Oxazolidinone, 3-cyclohexyl-5-phenyl- 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: 95.0%

: 27159-37-1
2-phenyl-1-cyclohexylcycloethylimine

: 124-38-9,18923-20-1
carbon dioxide

: 56805-21-1
N-cyclohexyl-5-phenyloxazolidin-2-one

Guidance literature:: With L-histidine; at 110 ℃; for 36h; under 60006 Torr; regioselective reaction; Autoclave; neat (no solvent);
DOI:10.1016/j.tetlet.2009.12.031

Reference yield: 54.0%

: 96-09-3
styrene oxide

: 3712-40-1
tert-butyl cyclohexylcarbamate

: 56805-21-1
N-cyclohexyl-5-phenyloxazolidin-2-one

Guidance literature:: With potassium tert-butylate; In N,N-dimethyl-formamide; at 20 ℃; for 48h;

Reference yield:

: 27159-37-1
2-phenyl-1-cyclohexylcycloethylimine

: 124-38-9,18923-20-1
carbon dioxide

: 56805-21-1
N-cyclohexyl-5-phenyloxazolidin-2-one

: N-cyclohexyl-4-phenyloxazolidin-2-one

Guidance literature:: With dmap; [N,N'-bis(3,5-ditBuC₆H₂CH-2-O-)-1,2-diN-cyclohexan]ClCr(III); In dichloromethane; at 100 ℃; for 16h; under 20685.9 Torr;
DOI:10.1021/ol049689t