🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
16783
CAS Number:
943449-15-8
Boc-L-3-carbamoylphenylalanine
Purity:
≥ 99.5% (Chiral HPLC)
Synonym(s):
Boc-(2S)-2-amino-3-(3-carbamoylphenyl)propanoic acid
Documents
$100.00 /250MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-L-3-carbamoylphenylalanine is a versatile amino acid derivative that plays a significant role in peptide synthesis and pharmaceutical research. 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, characterized by the 3-carbamoylphenyl group, allows for specific interactions in biological systems, which can be leveraged in drug development and therapeutic applications.

In the realm of medicinal chemistry, Boc-L-3-carbamoylphenylalanine is particularly valuable for the synthesis of bioactive peptides and compounds with potential anti-cancer and anti-inflammatory properties. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups makes it a preferred choice among chemists. Additionally, its applications extend to the development of novel drug delivery systems, where its properties can be utilized to enhance the efficacy and targeting of therapeutic agents.

Synonyms
Boc-(2S)-2-amino-3-(3-carbamoylphenyl)propanoic acid
CAS Number
943449-15-8
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C15H20N2O5
Molecular Weight
308.33
MDL Number
MFCD06659129
PubChem ID
22309167
Appearance
White solid
Optical Rotation
[a]D20 = -16 ± 2° (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-(2S)-2-amino-3-(3-carbamoylphenyl)propanoic acid
CAS Number
943449-15-8
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C15H20N2O5
Molecular Weight
308.33
MDL Number
MFCD06659129
PubChem ID
22309167
Appearance
White solid
Optical Rotation
[a]D20 = -16 ± 2° (C=1 in DMF)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-L-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 and biologically active compounds.
  • Drug Development: It plays a significant role in pharmaceutical research, especially in creating novel drugs that target specific biological pathways, enhancing the efficacy of treatments.
  • Bioconjugation: The chemical is used in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, improving their targeting and delivery.
  • Protein Engineering: It is applied in the field of protein engineering, where it aids in modifying proteins to enhance their stability and functionality for various applications.
  • Research in Cancer Therapeutics: The compound is being explored for its potential in cancer research, where it may contribute to the development of targeted therapies that can selectively attack cancer cells.

Citations