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Catalog Number:
16786
CAS Number:
1217637-40-5
Fmoc-D-3-carbamoylphénylalanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Acide Fmoc-(2 R -2-amino-3-(3-carbamoylphényl)propanoïque
Documents
$72.31 /100 mg
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Product Information

Fmoc-D-3-carbamoylphenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which facilitates the selective coupling of amino acids during solid-phase peptide synthesis. Its unique structure, characterized by the carbamoyl group on the phenylalanine side chain, enhances its stability and solubility, making it an ideal choice for researchers focused on developing complex peptides and biologically active compounds.

In pharmaceutical research, Fmoc-D-3-carbamoylphenylalanine serves as a crucial building block for synthesizing peptide-based therapeutics, including those targeting specific receptors or enzymes. Its application extends to the development of novel drug candidates with improved efficacy and reduced side effects. Additionally, this compound can be employed in the study of protein interactions and the design of biomaterials, showcasing its relevance across various fields, including medicinal chemistry and biochemistry.

Synonyms
Acide Fmoc-(2 R -2-amino-3-(3-carbamoylphényl)propanoïque
CAS Number
1217637-40-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C25H22N2O5
Molecular Weight
430.45
MDL Number
MFCD06659136
PubChem ID
53398424
Melting Point
194-200 ºC
Appearance
Solide blanc
Optical Rotation
[a] D 25 = +30 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Acide Fmoc-(2 R -2-amino-3-(3-carbamoylphényl)propanoïque
CAS Number
1217637-40-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C25H22N2O5
Molecular Weight
430.45
MDL Number
MFCD06659136
PubChem ID
53398424
Melting Point
194-200 ºC
Appearance
Solide blanc
Optical Rotation
[a] D 25 = +30 ± 2º (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-D-3-carbamoylphenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides with high purity and yield.
  • Drug Development: Its unique structure enhances the design of peptide-based drugs, particularly in targeting specific biological pathways, making it valuable in pharmaceutical research.
  • Bioconjugation: The chemical is used in bioconjugation techniques to attach peptides to other biomolecules, facilitating the development of targeted therapies and diagnostic tools.
  • Protein Engineering: It plays a role in modifying proteins to improve their stability and functionality, which is essential in biotechnology and enzyme engineering.
  • Research on Cancer Therapeutics: This compound is being explored for its potential in developing novel cancer treatments, as it can be tailored to interact with specific cancer cell receptors.

Citations