1196886-62-0

Basic information

• Product Name: BOC-(S)-ALPHA-(3-FLUOROBENZYL)-PROLINE
• Synonyms: BOC-(S)-ALPHA-(3-FLUOROBENZYL)-PROLINE;Boc-(S)-a-(3-fluorobenzyl)proline;(S)-1-(tert-Butoxycarbonyl)-2-(3-fluorobenzyl)-pyrrolidine-2-carboxylic acid;Boc-(S)-α-(3-fluorobenzyl)-proline;(Tert-Butoxy)Carbonyl (S)-Alpha-(3-fluoro-benzyl)-Pro
• CAS NO: 1196886-62-0
• Molecular Formula: C17H22FNO4
• Molecular Weight: 323.36
• Product Categories: Alpha-Substituted Proline Analogs
• Mol File: 1196886-62-0.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: BOC-(S)-ALPHA-(3-FLUOROBENZYL)-PROLINE(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-(S)-ALPHA-(3-FLUOROBENZYL)-PROLINE(1196886-62-0)
• EPA Substance Registry System: BOC-(S)-ALPHA-(3-FLUOROBENZYL)-PROLINE(1196886-62-0)

Safety Data

• Hazardous Substances Data: 1196886-62-0(Hazardous Substances Data)

Usage

Description

BOC-(S)-ALPHA-(3-FLUOROBENZYL)-PROLINE is a chemical compound that belongs to the class of proline derivatives. It contains a BOC (tert-butyloxycarbonyl) protecting group, an S configuration at the alpha carbon, and a 3-fluorobenzyl moiety. Its unique structure makes it a valuable building block for creating diverse molecular structures with potential biological activity.

Uses

Used in Pharmaceutical Industry:
BOC-(S)-ALPHA-(3-FLUOROBENZYL)-PROLINE is used as a key intermediate in the synthesis and development of pharmaceuticals, particularly in the design of proline-based drugs and peptidomimetics. Its unique structure allows for the creation of diverse molecular structures with potential biological activity.
Used in Drug Discovery:
BOC-(S)-ALPHA-(3-FLUOROBENZYL)-PROLINE has been studied for its potential applications in drug discovery, where it can be used to develop new compounds with therapeutic properties.
Used in Protein Engineering:
BOC-(S)-ALPHA-(3-FLUOROBENZYL)-PROLINE can be utilized in protein engineering to modify the structure and function of proteins, potentially leading to the development of novel biotherapeutics.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
BOC-(S)-ALPHA-(3-FLUOROBENZYL)-PROLINE serves as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of enantiomerically pure compounds, which is crucial in the production of pharmaceuticals and other chiral molecules.