339531-50-9

Basic information

• Product Name: (4S,5R)-3-(FMOC-ILE)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID
• Synonyms: (4S,5R)-3-(FMOC-ILE)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID;FMOC-ILE-THR(PSIME,MEPRO)-OH;Fmoc-L-Leu-L-Ser[PSI(Me,Me)Pro]-OH;(4S)-3-[(2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-methyl-1-oxopentyl]-2,2-dimethyl-4-oxazolidinecarboxylic acid;(S)-3-[N-(9-Fluorenylmethyloxycarbonyl)-L-leucinyl]-2,2-dimethyloxazolidine-4-carboxylic acid;Fmoc-Leu-Ser[Psi(Me,Me)Pro]-OH≥ 99% (HPLC);(S)-3-(N-Fmoc-L-leucinyl)-2,2-dimethyloxazolidine-4-carboxylic acid;(9H-Fluoren-9-yl)MethOxy]Carbonyl Leu-SerPsi(Me,Me)Pro-OH
• CAS NO: 339531-50-9
• Molecular Formula: C32H43N3O6
• Molecular Weight: 565.7
• Product Categories: peptide
• Mol File: 339531-50-9.mol
• Article Data: 0

Chemical Properties

• Appearance: /Solid
• Storage Temp.: -15°C
• CAS DataBase Reference: (4S,5R)-3-(FMOC-ILE)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5R)-3-(FMOC-ILE)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID(339531-50-9)
• EPA Substance Registry System: (4S,5R)-3-(FMOC-ILE)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID(339531-50-9)

Safety Data

• Hazardous Substances Data: 339531-50-9(Hazardous Substances Data)

Usage

Description

(4S,5R)-3-(FMOC-ILE)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is a chiral compound characterized by its specific stereochemistry, with the 4S,5R configuration. It is a white to off-white powder and is known for its potential applications in various fields due to its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
(4S,5R)-3-(FMOC-ILE)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is used as a building block for the synthesis of various pharmaceutical compounds. Its chiral nature and unique structure make it a valuable component in the development of new drugs with improved efficacy and selectivity.
Used in Chemical Synthesis:
(4S,5R)-3-(FMOC-ILE)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is used as an intermediate in the synthesis of complex organic molecules. Its specific stereochemistry allows for the creation of enantiomerically pure compounds, which are essential in various chemical reactions and applications.
Used in Research and Development:
(4S,5R)-3-(FMOC-ILE)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is used as a research tool for studying the properties and behavior of chiral compounds. Its unique structure provides insights into the development of new synthetic methods and the understanding of stereoselective reactions.