319009-76-2

Basic information

• Product Name: (R)-BoroSer(OBn)-(+)-Pinanediol-HCl
• Synonyms: (R)-BoroSer(OBn)-(+)-Pinanediol-HCl;(R)-BoroSer(Bzl)-(+)-Pinanediol-HCl
• CAS NO: 319009-76-2
• Molecular Formula: C19H29BClNO3
• Molecular Weight: 365.70246
• Mol File: 319009-76-2.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R)-BoroSer(OBn)-(+)-Pinanediol-HCl(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-BoroSer(OBn)-(+)-Pinanediol-HCl(319009-76-2)
• EPA Substance Registry System: (R)-BoroSer(OBn)-(+)-Pinanediol-HCl(319009-76-2)

Safety Data

• Hazardous Substances Data: 319009-76-2(Hazardous Substances Data)

Usage

Description

(R)-BoroSer(OBn)-(+)-Pinanediol-HCl is a chemical compound that consists of a boron-substituted serine amino acid derivative and pinanediol hydrochloride. It is commonly used as a catalyst in organic synthesis, particularly in asymmetric reactions. (R)-BoroSer(OBn)-(+)-Pinanediol-HCl is known for its ability to facilitate enantioselective transformations, making it a valuable tool in the production of chiral pharmaceuticals and fine chemicals. Its unique structure and properties allow for efficient and precise control over the stereochemistry of chemical reactions, making it an important component in the development of new synthetic methods and drug discovery.

Uses

Used in Pharmaceutical Industry:
(R)-BoroSer(OBn)-(+)-Pinanediol-HCl is used as a catalyst for enantioselective transformations in the production of chiral pharmaceuticals. Its ability to control the stereochemistry of chemical reactions is crucial for the synthesis of biologically active compounds with desired chiral properties.
Used in Fine Chemicals Industry:
(R)-BoroSer(OBn)-(+)-Pinanediol-HCl is used as a catalyst in the synthesis of fine chemicals, where the precise control of stereochemistry is essential for the development of high-quality products with specific applications.
Used in Research and Development:
(R)-BoroSer(OBn)-(+)-Pinanediol-HCl is used as a research tool for the development of new synthetic methods and drug discovery. Its unique properties make it an important component in the exploration of novel chemical reactions and the creation of innovative pharmaceutical compounds.