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Catalog Number:
02587
CAS Number:
76985-10-9
Boc-3-(2-naphthyl)-D-alanine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-D-Ala(2-naphthyl)-OH, Boc-(R-2-amino-3-(naphthalen-2-yl)propanoic acid
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Product Information

Boc-3-(2-naphthyl)-D-alanine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is characterized by its unique structure, which includes a naphthalene moiety that enhances its hydrophobic properties, making it particularly useful in the design of bioactive peptides. Its Boc (tert-butyloxycarbonyl) protecting group allows for easy manipulation during synthesis, providing researchers with a reliable tool for creating complex peptide sequences.

In pharmaceutical research, Boc-3-(2-naphthyl)-D-alanine is often utilized in the development of peptide-based therapeutics, especially in studies targeting specific receptors or pathways. Its ability to mimic natural amino acids while providing distinct properties makes it an attractive candidate for drug design. Additionally, this compound has shown potential in the field of materials science, where it can be incorporated into polymeric systems to enhance mechanical properties. With its diverse applications, Boc-3-(2-naphthyl)-D-alanine stands out as a valuable asset for researchers and industry professionals seeking innovative solutions in peptide chemistry and beyond.

Synonyms
Boc-D-Ala(2-naphthyl)-OH, Boc-(R-2-amino-3-(naphthalen-2-yl)propanoic acid
CAS Number
76985-10-9
Purity
≥ 99% (HPLC)
Molecular Formula
C18H21NO4
Molecular Weight
315.2
MDL Number
MFCD00076900
PubChem ID
3645897
Melting Point
96-103 ?C
Appearance
White solid
Optical Rotation
[a]D20 = -43 ± 2 º (C=1.049 in ethanol)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-Ala(2-naphthyl)-OH, Boc-(R-2-amino-3-(naphthalen-2-yl)propanoic acid
CAS Number
76985-10-9
Purity
≥ 99% (HPLC)
Molecular Formula
C18H21NO4
Molecular Weight
315.2
MDL Number
MFCD00076900
PubChem ID
3645897
Melting Point
96-103 ?C
Appearance
White solid
Optical Rotation
[a]D20 = -43 ± 2 º (C=1.049 in ethanol)
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-(2-naphthyl)-D-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in creating modified peptides that can enhance biological activity.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for developing new drugs, especially those targeting specific receptors due to its structural properties.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the functionality of drugs and diagnostics.
  • Research in Neuroscience: Its unique structure makes it useful in studies related to neurotransmitter activity, helping researchers understand brain function and develop treatments for neurological disorders.
  • Material Science: The compound is also explored in the development of novel materials, particularly in creating polymers with specific properties for applications in coatings and adhesives.

Citations