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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-Oxazolidineacetic acid, 2-oxo-4-phenyl-, (4S)-

OC(=O)CN1C(=O)OC[C@@H]1c1ccccc1 Request for Quotation
Chemical Name: 3-Oxazolidineacetic acid, 2-oxo-4-phenyl-, (4S)-
CAS Number: 99333-54-7
Product Number: AG0065ZB(AGN-PC-0OP4KH)
Synonyms:
MDL No:
Molecular Formula: C11H11NO4
Molecular Weight: 221.2093

Identification/Properties

Properties
MP:
103-105 °C(lit.)
BP:
516.4°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
221.212g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
221.069g/mol
Monoisotopic Mass:
221.069g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
286
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-2-(2-oxo-4-phenyloxazolidin-3-yl)acetic acid serves as a crucial building block in chemical synthesis processes due to its chirality and versatile reactivity. Its unique molecular structure lends itself to a variety of applications, particularly in the field of asymmetric synthesis. By incorporating this compound into reaction schemes, chemists can achieve stereochemical control in the formation of complex molecules.This compound can act as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals where precise stereochemistry is essential. The presence of the oxazolidinone moiety allows for selective reactions with nucleophiles or electrophiles, enabling the synthesis of enantiopure compounds. Furthermore, the phenyl group provides additional functionalization opportunities, enhancing the molecule's adaptability in diverse synthetic pathways.Overall, the (S)-2-(2-oxo-4-phenyloxazolidin-3-yl)acetic acid is a valuable tool for chemists seeking to design efficient and stereocontrolled synthetic routes for the production of complex organic molecules with high enantiomeric purity.