(R)-4-Phenyloxazolidine-2,5-dione

Base Information

Chemical Name:(R)-4-Phenyloxazolidine-2,5-dione
CAS No.:3412-49-5
Molecular Formula:C9H7 N O3
Molecular Weight:177.159
Hs Code.:2934999090
DSSTox Substance ID:DTXSID701298073
Nikkaji Number:J2.261.986A
Mol file:3412-49-5.mol

Synonyms:(R)-4-PHENYLOXAZOLIDINE-2,5-DIONE;3412-49-5;(4R)-4-phenyl-1,3-oxazolidine-2,5-dione;MFCD04039341;DTXSID701298073;AC5945;(4R)-4-Phenyl-2,5-oxazolidinedione;AKOS024387418;2,5-Oxazolidinedione, 4-phenyl-, D-;(4R)-4alpha-Phenyloxazolidine-2,5-dione;2,5-Oxazolidinedione, 4-phenyl-, (R)-

Suppliers and Price of (R)-4-Phenyloxazolidine-2,5-dione

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

American Custom Chemicals Corporation
(R)-4-PHENYLOXAZOLIDINE-2,5-DIONE 95.00%
1G
$ 671.86

AK Scientific
(R)-4-Phenyloxazolidine-2,5-dione
5g
$ 728.00

AK Scientific
(R)-4-Phenyloxazolidine-2,5-dione
10g
$ 1342.00

Activate Scientific
(R)-4-Phenyloxazolidine-2,5-dione 95+% ee
5 g
$ 760.00

Activate Scientific
(R)-4-Phenyloxazolidine-2,5-dione 95+% ee
1 g
$ 239.00

Total 10 raw suppliers

Chemical Property of (R)-4-Phenyloxazolidine-2,5-dione

Chemical Property:

Melting Point:123-126°C
PSA：55.40000
LogP:1.32290
XLogP3:1.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:177.042593085
Heavy Atom Count:13
Complexity:233

Purity/Quality:

97% ^*data from raw suppliers

(R)-4-PHENYLOXAZOLIDINE-2,5-DIONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 22-24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2C(=O)OC(=O)N2
Isomeric SMILES:C1=CC=C(C=C1)[C@@H]2C(=O)OC(=O)N2

Technology Process of (R)-4-Phenyloxazolidine-2,5-dione

There total 2 articles about (R)-4-Phenyloxazolidine-2,5-dione 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: 80.8%

: 17609-52-8
Z-D-phenylglycine

: 3412-49-5
N-carboxy-(R)-phenylglycine anhydride

Guidance literature:: With thionyl chloride; In benzene; at 45 ℃; for 3h;
DOI:10.1246/bcsj.67.748

Reference yield:

: 75-44-5
phosgene

: 875-74-1
(R)-phenylglycine

: 3412-49-5
N-carboxy-(R)-phenylglycine anhydride

Guidance literature:: In 1,4-dioxane;
DOI:10.1021/jo01032a505

Reference yield: 44.0%

: 371-96-0,37468-00-1
(E)-3,3,3-trifluoro-1-nitroprop-1-ene

: 3412-49-5
N-carboxy-(R)-phenylglycine anhydride

: (R)-Phenyl-(2,2,2-trifluoro-1-nitromethyl-ethylamino)-acetic acid

Guidance literature:: N-carboxy-(R)-phenylglycine anhydride; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃;

(E)-3,3,3-trifluoro-1-nitroprop-1-ene; In tetrahydrofuran; hexane; at -78 ℃;
DOI:10.1016/j.tetlet.2005.10.116