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Catalog Number:
16784
CAS Number:
205126-71-2
Boc-L-4-carbamoylphénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide boc-(2 S -2-amino-3-(4-carbamoylphényl)propanoïque
Documents
$154.93 /250 mg
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Product Information

Boc-L-4-carbamoylphenylalanine is a versatile amino acid derivative that plays a significant role in peptide synthesis and drug development. This compound is particularly valued in the pharmaceutical industry for its ability to enhance the stability and bioavailability of peptides. Its unique structure, featuring a carbamoyl group, allows for improved interactions in biological systems, making it an excellent candidate for research in medicinal chemistry and biochemistry. Researchers utilize Boc-L-4-carbamoylphenylalanine in the design of novel therapeutics, especially in the development of peptide-based drugs that target specific biological pathways.

In addition to its applications in drug formulation, Boc-L-4-carbamoylphenylalanine is also used in the synthesis of complex biomolecules, where it serves as a building block for more intricate structures. Its ability to facilitate the formation of peptide bonds under mild conditions makes it a preferred choice for chemists looking to streamline their synthesis processes. The compound's stability and compatibility with various coupling reagents further enhance its utility in laboratory settings, providing researchers with a reliable tool for advancing their projects.

Synonyms
Acide boc-(2 S -2-amino-3-(4-carbamoylphényl)propanoïque
CAS Number
205126-71-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C15H20N2O5
Molecular Weight
308.33
MDL Number
MFCD01317030
PubChem ID
6915695
Melting Point
303-307 °C (déc.)
Appearance
Solide blanc
Optical Rotation
[α] D 25 = -18,0 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Acide boc-(2 S -2-amino-3-(4-carbamoylphényl)propanoïque
CAS Number
205126-71-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C15H20N2O5
Molecular Weight
308.33
MDL Number
MFCD01317030
PubChem ID
6915695
Melting Point
303-307 °C (déc.)
Appearance
Solide blanc
Optical Rotation
[α] D 25 = -18,0 ± 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

Boc-L-4-carbamoylphenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require specific amino acid modifications. Its unique structure allows for the incorporation of functional groups that enhance peptide stability and activity.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates, especially in the development of targeted therapies for various diseases, including cancer. Its ability to modify biological activity makes it valuable in medicinal chemistry.
  • Bioconjugation: The compound is employed in bioconjugation processes, where it can be linked to biomolecules such as antibodies or enzymes. This application is crucial in the creation of targeted drug delivery systems and diagnostic tools.
  • Protein Engineering: Researchers use it to engineer proteins with enhanced properties, such as increased solubility or stability. This is particularly important in the production of therapeutic proteins and enzymes.
  • Research in Neuroscience: Its derivatives are being explored for their potential roles in neurobiology, particularly in the study of neurotransmitter systems and neuroprotective agents.

Citations