1252686-51-3

Basic information

• Product Name: 1-[(4R)-4-(1-Methylethyl)-2-thioxo-3-oxazolidinyl]-
• Synonyms: 1-[(4R)-4-(1-Methylethyl)-2-thioxo-3-oxazolidinyl]-;1-[(4R)-4-(1-Methylethyl)-2-thioxo-3-oxazolidinyl]-1-pro panone;1-[(4R)-4-Isopropyl-2-thioxo-3-oxazolidinyl]-1-propanone,99%e.e.;1-[(4R)-4-Isopropyl-2-thioxo-3-oxazolidinyl]-1-propanone
• CAS NO: 1252686-51-3
• Molecular Formula: C9H15NO2S
• Molecular Weight: 201.29
• Mol File: 1252686-51-3.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-[(4R)-4-(1-Methylethyl)-2-thioxo-3-oxazolidinyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[(4R)-4-(1-Methylethyl)-2-thioxo-3-oxazolidinyl]-(1252686-51-3)
• EPA Substance Registry System: 1-[(4R)-4-(1-Methylethyl)-2-thioxo-3-oxazolidinyl]-(1252686-51-3)

Safety Data

• Hazardous Substances Data: 1252686-51-3(Hazardous Substances Data)

Usage

Molecular structure

The compound has a thioxo-oxazolidinyl ring and a 1-methylethyl group attached to a chiral center.

Chirality

The presence of a chiral center (4R) in the molecule indicates that it has stereoisomers, which can have different biological activities.

Pharmaceutical applications

It is commonly used as a building block in the synthesis of various pharmaceuticals, including antibiotics and antiviral medications.

Biological activity

The compound has potential biological activity and is studied for its antibacterial and antifungal properties.

Drug development

Its unique structure makes it a valuable starting material for creating new drug molecules with improved efficacy and reduced side effects.

Chemical properties

The thioxo-oxazolidinyl ring and the 1-methylethyl group contribute to the compound's reactivity and its ability to form various derivatives.

Stereochemistry

The stereochemistry of the chiral center (4R) plays a crucial role in determining the compound's biological activity and its interactions with target molecules.

Synthesis

The compound can be synthesized through various chemical reactions, allowing for the exploration of different synthetic routes and optimization of the process.

Structural diversity

The presence of a chiral center and the thioxo-oxazolidinyl ring allows for the generation of a wide range of structurally diverse analogs with potential applications in drug discovery.

Research focus

The compound is a subject of ongoing research, with scientists investigating its potential applications in the development of new therapeutic agents and understanding its mode of action.