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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)-

2-Oxazolidinone, 3-(3-methyl-1-oxobutyl)-4-(phenylmethyl)-, (4S)-

CC(CC(=O)N1C(=O)OC[C@@H]1Cc1ccccc1)C Request for Quotation
Chemical Name: 2-Oxazolidinone, 3-(3-methyl-1-oxobutyl)-4-(phenylmethyl)-, (4S)-
CAS Number: 104266-90-2
Product Number: AG00864N(AGN-PC-0NVQ10)
Synonyms:
MDL No:
Molecular Formula: C15H19NO3
Molecular Weight: 261.3163

Identification/Properties

Computed Properties
Molecular Weight:
261.321g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
261.136g/mol
Monoisotopic Mass:
261.136g/mol
Topological Polar Surface Area:
46.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
334
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-4-Benzyl-3-(3-methylbutanoyl)oxazolidin-2-one, also known as $name$, is a key compound in chemical synthesis due to its versatile applications. It serves as a chiral auxiliary in asymmetric synthesis, particularly in the formation of enantiopure compounds. By utilizing $name$ as a chiral building block, chemists can control the stereochemistry of reactions, leading to the selective formation of desired enantiomers. This compound plays a crucial role in the production of pharmaceuticals, agrochemicals, and fine chemicals where chirality is essential for biological activity or product performance. Its unique structure enables the precise manipulation of stereochemistry, making it a valuable tool in the hands of synthetic chemists.