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Catalog Number:
15230
CAS Number:
190190-49-9
Boc-(1-naphtyl)-D-β-homoalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-D-β-HomoAla(1-naphtyl)-OH, Acide boc-( R -3-amino-4-(1-naphtyl)butyrique
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$127.79 /250 mg
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Product Information

Boc-(1-naphthyl)-D-b-homoalanine is a versatile amino acid derivative that plays a significant role in peptide synthesis and drug development. This compound features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for researchers working on complex peptide sequences. Its unique structure, characterized by the naphthyl group, not only contributes to its hydrophobic properties but also facilitates interactions in biological systems, making it valuable in medicinal chemistry and biochemistry applications.

This compound is particularly useful in the synthesis of bioactive peptides and can be employed in the development of pharmaceuticals targeting various diseases. Its ability to serve as a building block for more complex molecules allows researchers to explore new therapeutic avenues. Additionally, Boc-(1-naphthyl)-D-b-homoalanine's compatibility with various coupling reagents and its ease of deprotection make it a preferred choice for chemists aiming to streamline their synthesis processes. With its unique properties and practical applications, this compound is an essential tool for professionals in the fields of drug discovery and peptide research.

Synonyms
Boc-D-β-HomoAla(1-naphtyl)-OH, Acide boc-( R -3-amino-4-(1-naphtyl)butyrique
CAS Number
190190-49-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 19 H 234
Molecular Weight
329.4
MDL Number
MFCD01076281
PubChem ID
53397913
Appearance
Solide blanc
Optical Rotation
[a] D 25 = + 66 ± 2 º (C=1 dans l'éthanol)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Boc-D-β-HomoAla(1-naphtyl)-OH, Acide boc-( R -3-amino-4-(1-naphtyl)butyrique
CAS Number
190190-49-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 19 H 234
Molecular Weight
329.4
MDL Number
MFCD01076281
PubChem ID
53397913
Appearance
Solide blanc
Optical Rotation
[a] D 25 = + 66 ± 2 º (C=1 dans l'éthanol)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-(1-naphthyl)-D-b-homoalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids, which is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: Its unique structure makes it valuable in the design of new drugs, particularly in targeting specific biological pathways, enhancing efficacy, and reducing side effects.
  • Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules to create targeted therapies, such as antibody-drug conjugates, which improve treatment precision in cancer therapy.
  • Research in Neuroscience: It plays a role in studying neuropeptides and their receptors, contributing to the understanding of neurological disorders and potential treatments.
  • Material Science: The compound is explored in the development of novel materials with specific properties, such as enhanced stability or bioactivity, useful in various industrial applications.

Citations