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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, 4-(1H-indol-3-ylmethyl)-, (4S)-

O=C1OC[C@@H](N1)Cc1c[nH]c2c1cccc2 Request for Quotation
Chemical Name: 2-Oxazolidinone, 4-(1H-indol-3-ylmethyl)-, (4S)-
CAS Number: 152153-01-0
Product Number: AG006UC8(AGN-PC-0O4BYK)
Synonyms:
MDL No:
Molecular Formula: C12H12N2O2
Molecular Weight: 216.2359

Identification/Properties

Properties
MP:
157-160°C(lit.)
BP:
544.4°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-4-((1H-Indol-3-yl)methyl)oxazolidin-2-one is a versatile compound commonly utilized in chemical synthesis due to its unique structure and reactivity. This chiral oxazolidinone derivative serves as a valuable building block in the preparation of various biologically active molecules and pharmaceutical compounds.In chemical synthesis, (S)-4-((1H-Indol-3-yl)methyl)oxazolidin-2-one can function as a key intermediate in asymmetric synthesis strategies. Its oxazolidinone moiety facilitates the formation of enantioselective carbon-carbon and carbon-nitrogen bonds, making it an essential component in the creation of complex organic molecules with high optical purity.Furthermore, the presence of the indole group in the structure of this compound imparts additional functionality and versatility, enabling further derivatization to access a wide range of molecular scaffolds with potential biological activity.Overall, the application of (S)-4-((1H-Indol-3-yl)methyl)oxazolidin-2-one in chemical synthesis offers significant potential for the efficient and selective construction of structurally diverse compounds, making it a valuable tool for synthetic chemists in the development of novel pharmaceuticals, agrochemicals, and other fine chemicals.