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Catalog Number:
16615
CAS Number:
99395-88-7
S-(+)-4-Phenyl-2-oxazolidinone
Purity:
≥ 99% (HPLC)
Synonym(s):
(S-(+)-4-Phenyloxazolidin-2-one, L-(+)-4-(4S-Phenyloxazolidinone
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Product Information

(S)-(+)-4-Phenyl-2-oxazolidinone is a versatile chiral auxiliary widely utilized in organic synthesis and pharmaceutical development. This compound is recognized for its ability to facilitate asymmetric synthesis, making it invaluable in the production of enantiomerically pure compounds. Its unique oxazolidinone structure allows for selective reactions, which are crucial in the synthesis of various bioactive molecules, including pharmaceuticals and agrochemicals. Researchers appreciate its role in enhancing reaction efficiency and yield, particularly in the synthesis of amino acids and other chiral intermediates.

In addition to its synthetic applications, (S)-(+)-4-Phenyl-2-oxazolidinone is also employed in the development of novel drug candidates, where its chiral properties can influence biological activity and pharmacokinetics. Its use in medicinal chemistry has led to the discovery of compounds with improved efficacy and reduced side effects. With its proven track record in enhancing the quality of synthetic processes, this compound stands out as a critical tool for chemists aiming to innovate and optimize their research and development efforts.

Synonyms
(S-(+)-4-Phenyloxazolidin-2-one, L-(+)-4-(4S-Phenyloxazolidinone
CAS Number
99395-88-7
Purity
≥ 99% (HPLC)
Molecular Formula
C9H9NO2
Molecular Weight
163.17
MDL Number
MFCD00043396
PubChem ID
349728
Melting Point
134-137?C.
Appearance
White or off-white crystalline powder
Conditions
Store at 0-8 °C
General Information
Synonyms
(S-(+)-4-Phenyloxazolidin-2-one, L-(+)-4-(4S-Phenyloxazolidinone
CAS Number
99395-88-7
Purity
≥ 99% (HPLC)
Molecular Formula
C9H9NO2
Molecular Weight
163.17
MDL Number
MFCD00043396
PubChem ID
349728
Melting Point
134-137?C.
Appearance
White or off-white crystalline powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-(+)-4-Phenyl-2-oxazolidinone is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a chiral auxiliary in the synthesis of various pharmaceuticals, enhancing the production of enantiomerically pure drugs, which is crucial for efficacy and safety.
  • Asymmetric Synthesis: It plays a significant role in asymmetric synthesis, allowing chemists to create specific molecular configurations that are essential in developing targeted therapies.
  • Biochemical Research: Researchers use this compound in studies related to enzyme catalysis and reaction mechanisms, helping to understand biological processes at a molecular level.
  • Material Science: It is applied in the development of novel materials, particularly in creating polymers with unique properties, which can be used in various industrial applications.
  • Chiral Resolution: This chemical is effective in the chiral resolution of racemic mixtures, providing a method to separate and purify desired enantiomers, which is vital in many chemical and pharmaceutical processes.

Citations