1. Home
  2. 2-Oxazolidinone, 4-(2-methylpropyl)-, (4S)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-(2-methylpropyl)-, (4S)-

CC(C[C@H]1COC(=O)N1)C Request for Quotation
Chemical Name: 2-Oxazolidinone, 4-(2-methylpropyl)-, (4S)-
CAS Number: 17016-85-2
Product Number: AG00ACA3(AGN-PC-0O4TB5)
Synonyms:
MDL No:
Molecular Formula: C7H13NO2
Molecular Weight: 143.1836

Identification/Properties

Properties
BP:
300.9±9.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


(4S)-4-(2-Methylpropyl)-2-oxazolidinone, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it a valuable building block in the creation of various complex organic molecules. In chemical synthesis, $name$ serves as a chiral auxiliary, facilitating asymmetric synthesis by controlling the stereochemistry of reactions. This compound is particularly valuable in the preparation of pharmaceutical compounds, agrochemicals, and fine chemicals where precise stereochemical control is crucial for biological activity and efficiency. Moreover, $name$ can be utilized as a key intermediate in the synthesis of diverse compounds due to its reactivity and stability under various reaction conditions. Its utility extends across multiple synthetic methodologies, making it an indispensable tool for the efficient and selective creation of important molecules in the field of organic chemistry.