273401-69-7

Usage

Uses

Used in Pharmaceutical Industry:
(S)-2-amino-3-(tritylthio)propan-1-ol is used as a key building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of complex molecules with specific stereochemistry, which is crucial for the development of effective and targeted drugs.
Used in Agrochemical Industry:
In the agrochemical sector, (S)-2-amino-3-(tritylthio)propan-1-ol serves as an essential component in the synthesis of pesticides and other chemical products. Its ability to form a wide range of chemical bonds enables the development of innovative and efficient agrochemicals.
Used in Material Science:
(S)-2-amino-3-(tritylthio)propan-1-ol is used as a component in the research and development of novel materials. Its unique properties and bonding capabilities make it a promising candidate for the creation of advanced materials with specific characteristics and applications.
Used in Organic Synthesis Methodology:
This chiral compound is used as a key component in the development of new chemical reactions and methodologies in organic synthesis. Its versatility in forming various chemical bonds allows researchers to explore new pathways and techniques for synthesizing complex molecules.

Upstream product

• 2799-07-7 S-trityl-L-cysteine 
• 921-01-7 D-cysteine 
• 76-83-5 trityl chloride 
• 125509-78-6 (R)-cysteinol 

Relevant academic research and scientific papers

TRICYCLIC COMPOUNDS

The present invention provides a compound of formula I or a pharmaceutically acceptable salt thereof; and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

Selective inhibitors of EG5 motors and methods of use

Embodiments of the present invention comprises a compound of formula I or its enantiomer, diastereomer, stereoisomer or its pharmaceutically acceptable salt, methods of use and methods of synthesis.

Synthesis and characterization of tritylthioethanamine derivatives with potent KSP inhibitory activity

Assembly of a bipolar mitotic spindle requires the action of class 5 kinesins, and inhibition or depletion of this motor results in mitotic arrest and apoptosis. S-Trityl-l-cysteine is an allosteric inhibitor of vertebrate Kinesin Spindle Protein (KSP) th

Aminosulf(ox)ides as Ligands for Iridium(I)-Catalyzed Asymmetric Transfer Hydrogenation

A new class of efficient catalysts was developed for the asymmetric transfer hydrogenation of unsymmetrical ketones. A series of chiral N,S-chelates (6-22) was synthesized to serve as ligands in the iridium(I)-catalyzed reduction of ketones. Both formic a