790305-00-9

Basic information

• Product Name: (S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid
• Synonyms: (S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid;(S)-2-((tert-Butoxycarbonyl)aMino)-3-(pent-4-en-1-yloxy)propanoic acid
• CAS NO: 790305-00-9
• Molecular Formula: C₁₃H₂₃NO₅
• Molecular Weight: 273.32542
• Mol File: 790305-00-9.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 412.9±45.0 °C(Predicted)
• Appearance: /
• Density: 1.084±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 3.54±0.10(Predicted)
• CAS DataBase Reference: (S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid(790305-00-9)
• EPA Substance Registry System: (S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid(790305-00-9)

Safety Data

• Hazardous Substances Data: 790305-00-9(Hazardous Substances Data)

Usage

Description

(S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid is a complex organic compound characterized by a propanoic acid core, with a tert-butoxycarbonylamino group and a pent-4-enyloxy side chain. The presence of a chiral center in its structure indicates the existence of stereoisomers, with the (S)-enantiomer being specifically denoted. (S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid is likely to have applications in medicinal and pharmaceutical chemistry due to the known anti-inflammatory and analgesic properties of propanoic acids, and the boc-protected amino group suggests its potential use in peptide synthesis or drug delivery systems.

Uses

Used in Pharmaceutical Industry:
(S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid is used as a pharmaceutical intermediate for the development of new drugs, leveraging its anti-inflammatory and analgesic properties inherent to propanoic acids.
Used in Peptide Synthesis:
In the field of organic chemistry, (S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid serves as a building block in peptide synthesis, where the boc-protected amino group is crucial for the stepwise assembly of peptide chains.
Used in Drug Delivery Systems:
(S)-2-(tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid is utilized in the design of drug delivery systems to improve the bioavailability and targeting of therapeutic agents, taking advantage of its structural features to enhance drug efficacy and reduce side effects.

Upstream product

• 2766-43-0 N-tert-butyloxycarbonyl-L-serine methyl ester 
• 1119-51-3 bromopentene 
• 3262-72-4 (S)-N-(tert-butoxycarbonyl)serine 
• 790304-99-3 2-tert-butoxycarbonylamino-3-pent-4-enyloxypropionic acid methyl ester 

Downstream Products

• 1338650-05-7 1-{[4-(4-bromobenzenesulfonyloxy)-1-(2-cyclopentyloxycarbonylamino-3-pent-4-enyloxypropionyl)pyrrolidine-2-carbonyl]amino}-2-vinylcyclopropanecarboxylic acid ethyl ester 
• 790304-99-3 2-tert-butoxycarbonylamino-3-pent-4-enyloxypropionic acid methyl ester 

Relevant articles and documents

Water-soluble poly(l -serine)s with elongated and charged side-chains: Synthesis, conformations, and cell-penetrating properties

Water-soluble poly(l-serine)s bearing long side-chain with terminal charge groups were synthesized via ring-opening polymerization of O-pentenyl-l-serine N-carboxyanhydride followed by thiol-ene reactions. These side-chain modified poly(l-serine)s adopt β

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Inhibitors of Hepatitis C Virus

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