Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
15239
CAS Number:
218608-84-5
Boc-(S-3-amino-5-phenylpentanoic acid
Purity:
≥ 98%
Synonym(s):
Boc-β-Nva(5-phenyl)-OH
Documents
$65.40 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-(S)-3-amino-5-phenylpentanoic acid is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an excellent choice for various applications in organic synthesis. Its unique structure allows for the selective incorporation of the amino acid into peptides, facilitating the development of novel therapeutics and biologically active compounds. Researchers appreciate its role in the synthesis of complex molecules, particularly in the fields of medicinal chemistry and drug discovery.

Additionally, Boc-(S)-3-amino-5-phenylpentanoic acid serves as a valuable building block for the preparation of bioactive peptides and can be employed in the design of enzyme inhibitors or receptor ligands. Its compatibility with standard coupling reagents and methodologies streamlines the synthesis process, making it a preferred choice among chemists. With its robust performance and application potential, this compound stands out as a key ingredient in advancing research and development in the pharmaceutical industry.

Synonyms
Boc-β-Nva(5-phenyl)-OH
CAS Number
218608-84-5
Purity
≥ 98%
Molecular Formula
C16H23NO4
Molecular Weight
293.36
MDL Number
MFCD01076264
PubChem ID
6915689
Appearance
White powder
Optical Rotation
[a]20D = -2.4 ± 1 º (C=1 in Ethanol)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-β-Nva(5-phenyl)-OH
CAS Number
218608-84-5
Purity
≥ 98%
Molecular Formula
C16H23NO4
Molecular Weight
293.36
MDL Number
MFCD01076264
PubChem ID
6915689
Appearance
White powder
Optical Rotation
[a]20D = -2.4 ± 1 º (C=1 in Ethanol)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(S)-3-amino-5-phenylpentanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions and improving yields in complex organic synthesis.
  • Drug Development: It plays a crucial role in the design of pharmaceutical compounds, particularly in creating bioactive peptides that can lead to new therapeutic agents.
  • Biotechnology: Used in the modification of proteins, enhancing their stability and activity, which is vital for biopharmaceutical applications.
  • Research in Neuroscience: Its derivatives are explored for potential neuroprotective effects, contributing to studies on neurodegenerative diseases.
  • Material Science: This compound is investigated for its potential in developing new materials with specific properties, such as improved biocompatibility for medical devices.

Citations