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Catalog Number:
16780
CAS Number:
1213190-47-6
Boc-D-3-carbamoylphenylalanine
Purity:
≥ 99% (Assay by titration on dried basis)
Synonym(s):
Boc-(2R-2-amino-3-(3-carbamoylphenyl)propanoic acid
Documents
$72.31 /250MG
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Product Information

Boc-D-3-carbamoylphenylalanine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for researchers working on complex peptide sequences. Its unique structure allows for the incorporation of a carbamoyl group, which can significantly influence the biological activity of peptides, thereby expanding its applications in medicinal chemistry and biochemistry.

In practical applications, Boc-D-3-carbamoylphenylalanine is utilized in the synthesis of bioactive peptides, which are essential in pharmaceutical research for developing new therapeutic agents. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups makes it invaluable in the production of peptide-based drugs. Additionally, this compound can be employed in studies related to protein engineering and enzyme activity modulation, providing researchers with a powerful tool for exploring new avenues in drug discovery and development.

Synonyms
Boc-(2R-2-amino-3-(3-carbamoylphenyl)propanoic acid
CAS Number
1213190-47-6
Purity
≥ 99% (Assay by titration on dried basis)
Molecular Formula
C15H20N2O5
Molecular Weight
308.33
MDL Number
MFCD06659120
PubChem ID
22309167
Melting Point
146 - 150 °C
Appearance
Almost white powder
Optical Rotation
[a]25D = -15 ± 1 º (C=1 in C2H5OH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-(2R-2-amino-3-(3-carbamoylphenyl)propanoic acid
CAS Number
1213190-47-6
Purity
≥ 99% (Assay by titration on dried basis)
Molecular Formula
C15H20N2O5
Molecular Weight
308.33
MDL Number
MFCD06659120
PubChem ID
22309167
Melting Point
146 - 150 °C
Appearance
Almost white powder
Optical Rotation
[a]25D = -15 ± 1 º (C=1 in C2H5OH)
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-D-3-carbamoylphenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of therapeutic agents. Its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: Researchers leverage its unique structure to design and optimize new drugs, especially those targeting specific biological pathways. This can lead to more effective treatments with fewer side effects.
  • Bioconjugation: The compound is used in bioconjugation processes, where it can be linked to other biomolecules. This is particularly useful in creating targeted drug delivery systems, improving the efficacy of treatments.
  • Research in Cancer Therapeutics: Its application in cancer research is notable, as it can be incorporated into compounds that inhibit tumor growth, providing a pathway for developing novel cancer therapies.
  • Analytical Chemistry: Boc-D-3-carbamoylphenylalanine is also utilized in analytical methods to study protein interactions and stability, aiding in the understanding of complex biological systems.

Citations