Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
29273
CAS Number:
145589-03-3
R -3-(3-Metilbutanoil)-4-benciloxazolidin-2-ona
Documents
$201.60 /100 mg
Tamaño
Request Bulk Quote
Product Information

(R)-3-(3-Methylbutanoyl)-4-benzyloxazolidin-2-one is a versatile compound with significant applications in pharmaceutical research and development. This chiral oxazolidinone derivative is recognized for its potential as a building block in the synthesis of bioactive molecules, particularly in the creation of novel antibiotics and other therapeutic agents. Its unique structure allows for the introduction of various functional groups, making it an invaluable tool for medicinal chemists aiming to enhance the efficacy and selectivity of drug candidates.

The compound's stability and compatibility with a range of reaction conditions further bolster its utility in organic synthesis. Researchers have utilized (R)-3-(3-Methylbutanoyl)-4-benzyloxazolidin-2-one in the development of chiral ligands and catalysts, which are crucial in asymmetric synthesis processes. Its ability to facilitate the formation of complex molecular architectures positions it as a key player in advancing drug discovery and development, particularly in the search for innovative treatments in infectious diseases.

CAS Number
145589-03-3
Molecular Formula
C15H19Nº3
Molecular Weight
261.32
MDL Number
MFCD10566718
PubChem ID
15597773
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
145589-03-3
Molecular Formula
C15H19Nº3
Molecular Weight
261.32
MDL Number
MFCD10566718
PubChem ID
15597773
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R)-3-(3-Methylbutanoyl)-4-benzyloxazolidin-2-one is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a valuable intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Chiral Synthesis: Its chiral nature makes it an essential component in asymmetric synthesis, allowing researchers to create more effective and selective drug molecules.
  • Biochemical Research: It is used in studies related to enzyme inhibition and protein interactions, providing insights into biological mechanisms and potential therapeutic targets.
  • Material Science: This compound can be incorporated into polymer formulations, enhancing their properties for applications in coatings and adhesives.
  • Cosmetic Formulations: Its stability and compatibility with various ingredients make it suitable for use in cosmetic products, contributing to improved texture and performance.

Citas