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Catalog Number:
16787
CAS Number:
1217610-39-3
Fmoc-D-4-carbamoilfenilalanina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido Fmoc-(2 R )-2-amino-3-(4-carbamoilfenil)propanoico
Documents
$60.00 /100 mg
Tamaño
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Product Information

Fmoc-D-4-carbamoylphenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during solid-phase peptide synthesis. Its unique structure, characterized by the presence of a carbamoyl group on the phenylalanine side chain, enhances the compound's stability and solubility, making it an excellent choice for researchers focused on developing complex peptides and biologically active compounds.

In practical applications, Fmoc-D-4-carbamoylphenylalanine is particularly valuable in the fields of medicinal chemistry and biochemistry, where it is employed in the synthesis of peptide-based therapeutics and in the study of protein interactions. Its ability to facilitate the incorporation of non-standard amino acids into peptides allows for the exploration of novel therapeutic agents with improved efficacy and specificity. Researchers appreciate its compatibility with various coupling reagents and its effectiveness in generating high-purity peptides, making it a preferred choice in both academic and industrial laboratories.

Synonyms
Ácido Fmoc-(2 R )-2-amino-3-(4-carbamoilfenil)propanoico
CAS Number
1217610-39-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C25H22N2O5
Molecular Weight
430.45
MDL Number
MFCD06659137
PubChem ID
6915696
Melting Point
239 - 245 °C (Literatura)
Appearance
Polvo/sólido blanco
Optical Rotation
[a] D 25 = 22 - 26 ° (C=1 en DMF) (Lit.)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido Fmoc-(2 R )-2-amino-3-(4-carbamoilfenil)propanoico
CAS Number
1217610-39-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C25H22N2O5
Molecular Weight
430.45
MDL Number
MFCD06659137
PubChem ID
6915696
Melting Point
239 - 245 °C (Literatura)
Appearance
Polvo/sólido blanco
Optical Rotation
[a] D 25 = 22 - 26 ° (C=1 en DMF) (Lit.)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-D-4-carbamoylphenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for various biological studies.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, particularly those targeting specific receptors or enzymes.
  • Bioconjugation: The chemical is used in bioconjugation processes, enabling the attachment of biomolecules to therapeutic agents, enhancing their efficacy and targeting capabilities.
  • Research in Cancer Therapy: It plays a role in developing targeted therapies for cancer, where specific peptide sequences can be designed to interact with cancer cells.
  • Protein Engineering: This compound aids in the modification of proteins, allowing scientists to study protein interactions and functions more effectively.

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