1217833-86-7

Basic information

• Product Name: (2S)-2-(2,6-DIFLUOROPHENYL)PYRROLIDINE
• Synonyms: (2S)-2-(2,6-DIFLUOROPHENYL)PYRROLIDINE
• CAS NO: 1217833-86-7
• Molecular Formula: C10H11F2N
• Molecular Weight: 183.2
• Mol File: 1217833-86-7.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2S)-2-(2,6-DIFLUOROPHENYL)PYRROLIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-2-(2,6-DIFLUOROPHENYL)PYRROLIDINE(1217833-86-7)
• EPA Substance Registry System: (2S)-2-(2,6-DIFLUOROPHENYL)PYRROLIDINE(1217833-86-7)

Safety Data

• Hazardous Substances Data: 1217833-86-7(Hazardous Substances Data)

Usage

Description

(2S)-2-(2,6-DIFLUOROPHENYL)PYRROLIDINE is a chiral pyrrolidine derivative with the molecular formula C10H12F2N. It features a 2,6-difluorophenyl group and possesses the (2S) configuration, indicating its stereochemistry. (2S)-2-(2,6-DIFLUOROPHENYL)PYRROLIDINE is valued in the pharmaceutical industry for its versatile chemical properties and potential biological activity, making it a useful building block in organic synthesis and a starting material for creating pharmacologically active compounds.

Uses

Used in Pharmaceutical Industry:
(2S)-2-(2,6-DIFLUOROPHENYL)PYRROLIDINE is used as a chiral building block for the synthesis of various drugs. Its unique stereochemistry and the presence of the 2,6-difluorophenyl group contribute to the development of molecules with specific therapeutic effects.
Used in Organic Synthesis:
In the field of organic synthesis, (2S)-2-(2,6-DIFLUOROPHENYL)PYRROLIDINE serves as a starting material for the preparation of complex organic compounds. Its versatile chemical properties allow for multiple synthetic pathways, leading to the creation of a wide range of molecules with potential applications in various industries.
Used in Drug Development:
(2S)-2-(2,6-DIFLUOROPHENYL)PYRROLIDINE is utilized in drug development as a precursor for the production of pharmacologically active compounds. Its role in creating molecules with specific biological activities makes it an essential component in the discovery and development of new medications.