850996-84-8

Basic information

• Product Name: (2S,4R)-5-BENZYLOXYCARBONYLAMINO-2-TERT-BUTOXYCARBONYLAMINO-4-TRIISOPROPYLSILANYLOXY-PENTANOIC ACID
• Synonyms: (2S,4R)-5-BENZYLOXYCARBONYLAMINO-2-TERT-BUTOXYCARBONYLAMINO-4-TRIISOPROPYLSILANYLOXY-PENTANOIC ACID;BOC-L-ORN(4R-OTIPS, 5-Z)-OH;(2S,4R)-5-BENZYLOXYCARBONYLAMINO-2-T-BUTOXYCARBONYLAMINO-4-TRIISOPROPYLSILANYLOXY-PENTANOIC ACID
• CAS NO: 850996-84-8
• Molecular Formula: C₂₇H₄₆N₂O₇Si
• Molecular Weight: 538.75
• Mol File: 850996-84-8.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2S,4R)-5-BENZYLOXYCARBONYLAMINO-2-TERT-BUTOXYCARBONYLAMINO-4-TRIISOPROPYLSILANYLOXY-PENTANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,4R)-5-BENZYLOXYCARBONYLAMINO-2-TERT-BUTOXYCARBONYLAMINO-4-TRIISOPROPYLSILANYLOXY-PENTANOIC ACID(850996-84-8)
• EPA Substance Registry System: (2S,4R)-5-BENZYLOXYCARBONYLAMINO-2-TERT-BUTOXYCARBONYLAMINO-4-TRIISOPROPYLSILANYLOXY-PENTANOIC ACID(850996-84-8)

Safety Data

• Hazardous Substances Data: 850996-84-8(Hazardous Substances Data)

Usage

Description

(2S,4R)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-4-triisopropylsilanyloxy-pentanoic acid is a complex amino acid derivative with a unique structure and functional groups. It contains benzyloxycarbonyl, tert-butoxycarbonyl, and triisopropylsilane groups, which contribute to its potential applications in various fields.

Uses

Used in Peptide Synthesis:
(2S,4R)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-4-triisopropylsilanyloxy-pentanoic acid is used as a building block for peptide synthesis due to its amine and carboxylic acid groups. These functional groups are essential for forming peptide bonds, making it a valuable component in the creation of new peptide-based compounds.
Used in Chemical and Biological Research:
(2S,4R)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-4-triisopropylsilanyloxy-pentanoic acid is used as a research tool in the fields of chemical and biological research. Its intricate structure and functional groups make it a valuable asset for studying peptide chemistry and exploring its potential applications in various industries.

Upstream product

• 850996-92-8 (2S,4R)-1-hydroxy-4-triisopropylsilanyloxy-5-benzyloxycarbonylaminopent-2-ylaminocarboxylic acid tert-butyl ester 
• 850996-87-1 (4S)-4-[2-(1-methoxy-1-methylethoxy)ethyl]-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 850996-90-6 (4S)-[(2R)-3-benzyloxycarbonylamino-2-triisopropylsilanyloxypropyl]-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 80522-42-5 triisopropylsilyl trifluoromethanesulfonate 
• 128427-10-1 (S)-2-(tert-butoxycarbonylamino)-1,4-butanediol 
• 128427-09-8 (S)-N-tert-butoxycarbonyl-aspartic acid diethyl ester 
• 147959-18-0 (4S)-2,2-dimethyl-4-(2-hydroxyethyl)oxazolidine-3-carboxylic acid tert-butyl ester 
• 147959-19-1 (4S)-2,2-dimethyl-3-(t-butoxycarbonyl)-4-(formylmethyl)-1,3-oxazolidine 

Downstream Products

• 329912-53-0 (3S,5R)-[5-(benzyloxycarbonylaminomethyl)-2-oxotetrahydrofuran-3-yl]carbamic acid tert-butyl ester 

Relevant articles and documents

IMPROVED PROCEDURE FOR THE PREPARATION OF (4S)- OR (4R)-2,2-DIMETHYL-4-(2-HYDROXETHYL)OXAZOLIDINE-3-CARBOXYLIC ACID ALKYL ESTERS

The present invention is directed to a process for the preparation of (4S)- or (4R)-2,2-dimethyl-4-(2-hydroxethyl)oxazolidine-3-carboxylic acid alkyl esters. The invention is further directed to an intermediate product from which those alkyl esters may be obtained.