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Catalog Number:
07412
CAS Number:
268733-63-7
Fmoc-3-(9-anthryl)-D-alanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-3-D-Ala(9-anthryl)-OH
Documents
$95.60 /25 mg
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Product Information

Fmoc-3-(9-anthryl)-D-alanine is a specialized amino acid derivative that plays a significant role in peptide synthesis and drug development. This compound features a unique anthracene moiety, which enhances its photophysical properties, making it particularly valuable in the fields of biochemistry and materials science. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection during peptide synthesis, facilitating the creation of complex peptide sequences with high purity and yield. Researchers utilize Fmoc-3-(9-anthryl)-D-alanine in the development of fluorescent probes, as well as in the study of protein interactions and conformational changes due to its ability to act as a chromophore.

In addition to its applications in research, this compound is also relevant in the pharmaceutical industry, where it can be used to design novel therapeutics with enhanced bioactivity. Its unique structural features provide advantages over similar compounds, particularly in terms of stability and solubility, making it an ideal choice for various applications. Whether you are involved in academic research or industrial applications, Fmoc-3-(9-anthryl)-D-alanine offers a versatile tool for advancing your projects.

Synonyms
Fmoc-3-D-Ala(9-anthryl)-OH
CAS Number
268733-63-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 32 H 354
Molecular Weight
487.55
MDL Number
MFCD02094462
PubChem ID
4225821
Melting Point
240 - 244 ºC (déc.)
Appearance
Poudre/solide jaunâtre clair à jaune
Optical Rotation
[a] D 20 = 35 ± 2 º (C = 1 dans DMF) D 25 = 30 ± 1 º (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-3-D-Ala(9-anthryl)-OH
CAS Number
268733-63-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 32 H 354
Molecular Weight
487.55
MDL Number
MFCD02094462
PubChem ID
4225821
Melting Point
240 - 244 ºC (déc.)
Appearance
Poudre/solide jaunâtre clair à jaune
Optical Rotation
[a] D 20 = 35 ± 2 º (C = 1 dans DMF) D 25 = 30 ± 1 º (C = 1 dans DMF)
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

Fmoc-3-(9-anthryl)-D-alanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide structures with high purity.
  • Fluorescent Probes: Its unique anthracene moiety makes it an excellent candidate for developing fluorescent probes, which are used in biological imaging to track cellular processes.
  • Drug Development: The compound is explored in the pharmaceutical industry for designing novel drug candidates, leveraging its ability to enhance the bioactivity of therapeutic peptides.
  • Material Science: It is applied in the development of advanced materials, particularly in organic electronics and photonic devices, due to its favorable electronic properties.
  • Bioconjugation: The compound facilitates bioconjugation techniques, enabling researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.

Citations