161384-85-6

Basic information

• Product Name: (2S,4S)-2-Methyl-4-(thiophen-3-yl)oxan-4-ol
• Synonyms: (2S,4S)-2-Methyl-4-(thiophen-3-yl)oxan-4-ol;161384-85-6;DTXSID20724650
• CAS NO: 161384-85-6
• Molecular Formula: C10H14O2S
• Molecular Weight: 198.28
• Mol File: 161384-85-6.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: (2S,4S)-2-Methyl-4-(thiophen-3-yl)oxan-4-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,4S)-2-Methyl-4-(thiophen-3-yl)oxan-4-ol(161384-85-6)
• EPA Substance Registry System: (2S,4S)-2-Methyl-4-(thiophen-3-yl)oxan-4-ol(161384-85-6)

Safety Data

• Hazardous Substances Data: 161384-85-6(Hazardous Substances Data)

Usage

Description

(2S,4S)-2-Methyl-4-(thiophen-3-yl)oxan-4-ol is a chiral organic compound characterized by a carbon backbone and a thiophenyl group. It has a molecular formula of C9H12OS and a molecular weight of 180.25 g/mol. As a stereoisomer, it possesses two stereocenters, and its IUPAC name is (2S,4S)-2-Methyl-4-(3-thienyl)tetrahydro-2H-pyran-4-ol. This unique structure endows it with potential applications in various fields.

Uses

Used in Organic Chemistry Research:
(2S,4S)-2-Methyl-4-(thiophen-3-yl)oxan-4-ol is utilized as a key intermediate in the synthesis of complex organic molecules. Its unique structure allows for the development of novel chemical reactions and the exploration of its reactivity, contributing to the advancement of organic chemistry.
Used in Pharmaceutical Development:
(2S,4S)-2-Methyl-4-(thiophen-3-yl)oxan-4-ol is employed as a lead compound in drug discovery. Its potential pharmacological properties make it a promising candidate for the development of new therapeutic agents. Researchers can use this compound to design and optimize drugs targeting specific biological pathways or diseases.
Used in Chiral Chemistry:
As a chiral molecule with two stereocenters, (2S,4S)-2-Methyl-4-(thiophen-3-yl)oxan-4-ol is used in the study of stereochemistry and its effects on chemical and biological processes. This knowledge can be applied to improve the selectivity and efficacy of chiral drugs and to understand the role of stereochemistry in biological systems.
Used in Material Science:
The unique structure of (2S,4S)-2-Methyl-4-(thiophen-3-yl)oxan-4-ol can be exploited in the development of new materials with specific properties. For example, it can be used to create chiral materials with applications in sensors, catalysts, or optoelectronics.