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Catalog Number:
15413
CAS Number:
270596-39-9
Boc-3-chloro-L-β-homophenylalanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-L-β-HomoPhe(3-Cl)-OH, Boc-(S)-3-amino-4-(3-chlorophenyl)butyric acid
Documents
$72.31 /100MG
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Product Information

Boc-3-chloro-L-b-homophenylalanine is a valuable 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 synthetic applications. Its unique structure, characterized by the presence of a chlorine atom on the aromatic ring, allows for selective modifications that can lead to the development of novel therapeutic agents. Researchers often employ Boc-3-chloro-L-b-homophenylalanine in the design of bioactive peptides, particularly in studies focused on drug delivery systems and protein engineering.

The compound's ability to serve as a building block in the synthesis of complex peptides positions it as a crucial tool in medicinal chemistry and biochemistry. Its compatibility with various coupling reactions further expands its utility in the development of peptide-based drugs. With its favorable properties and versatile applications, Boc-3-chloro-L-b-homophenylalanine stands out as a key ingredient for researchers aiming to innovate in the fields of drug discovery and development.

Synonyms
Boc-L-β-HomoPhe(3-Cl)-OH, Boc-(S)-3-amino-4-(3-chlorophenyl)butyric acid
CAS Number
270596-39-9
Purity
≥ 98% (HPLC)
Molecular Formula
C15H20ClNO4
Molecular Weight
313.78
MDL Number
MFCD01860999
PubChem ID
53398002
Melting Point
150 - 156 ºC
Appearance
White powder
Optical Rotation
[a]D25 = -13 ± 2 º (C=1 in EtOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-β-HomoPhe(3-Cl)-OH, Boc-(S)-3-amino-4-(3-chlorophenyl)butyric acid
CAS Number
270596-39-9
Purity
≥ 98% (HPLC)
Molecular Formula
C15H20ClNO4
Molecular Weight
313.78
MDL Number
MFCD01860999
PubChem ID
53398002
Melting Point
150 - 156 ºC
Appearance
White powder
Optical Rotation
[a]D25 = -13 ± 2 º (C=1 in EtOH)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-3-chloro-L-b-homophenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, particularly in the creation of modified peptides that can enhance therapeutic efficacy.
  • Drug Development: It is used in the pharmaceutical industry to develop new drugs, especially those targeting specific biological pathways, owing to its unique structural properties.
  • Bioconjugation: The compound is valuable in bioconjugation processes, allowing researchers to attach biomolecules to drugs, improving their delivery and targeting capabilities.
  • Research on Protein Interactions: It aids in studying protein interactions and functions, providing insights into cellular mechanisms that can lead to new therapeutic strategies.
  • Custom Synthesis: Many laboratories utilize this compound for custom synthesis projects, benefiting from its versatility in creating diverse chemical entities for various applications.

Citations