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Catalog Number:
16812
CAS Number:
1212864-47-5
Boc-D-2,4-dinitrophenylalanine
Synonym(s):
Boc-D-Phe(2,4-DiNO2)-OH, (R-Boc-2-amino-3-(2,4-dinitrophenyl)propionic acid
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$340.51 /1G
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Product Information

Boc-D-2,4-dinitrophenylalanine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and bioconjugation applications. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its unique dinitrophenyl group allows for selective labeling and detection in various assays, providing valuable insights in drug development and protein engineering.

In practical applications, Boc-D-2,4-dinitrophenylalanine is utilized in the synthesis of peptide-based therapeutics and as a building block in the creation of complex biomolecules. Its ability to facilitate the introduction of functional groups makes it a preferred choice for scientists looking to explore structure-activity relationships in drug design. Additionally, its compatibility with various coupling reactions ensures that it can be seamlessly integrated into existing workflows, enhancing efficiency and productivity in laboratory settings.

Synonyms
Boc-D-Phe(2,4-DiNO2)-OH, (R-Boc-2-amino-3-(2,4-dinitrophenyl)propionic acid
CAS Number
1212864-47-5
Molecular Formula
C14H17N3O8
Molecular Weight
355.3
MDL Number
MFCD08061617
PubChem ID
53398473
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-Phe(2,4-DiNO2)-OH, (R-Boc-2-amino-3-(2,4-dinitrophenyl)propionic acid
CAS Number
1212864-47-5
Molecular Formula
C14H17N3O8
Molecular Weight
355.3
MDL Number
MFCD08061617
PubChem ID
53398473
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-2,4-dinitrophenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of pharmaceuticals. Its unique structure allows for the introduction of specific functionalities that can enhance the biological activity of peptides.
  • Drug Development: In medicinal chemistry, it is used to create compounds with potential therapeutic effects. Researchers can modify its structure to improve drug efficacy and reduce side effects, making it a key player in drug discovery.
  • Protein Labeling: The dinitrophenyl group in this compound can be utilized for labeling proteins in biochemical assays. This application is crucial for studying protein interactions and functions, providing insights into cellular processes.
  • Analytical Chemistry: It is employed in various analytical techniques, such as chromatography and mass spectrometry, to identify and quantify amino acids and peptides. This helps in quality control and assurance in pharmaceutical manufacturing.
  • Bioconjugation: Boc-D-2,4-dinitrophenylalanine can be used in bioconjugation strategies to attach biomolecules to surfaces or other molecules. This is particularly beneficial in the development of targeted drug delivery systems and diagnostic tools.

Citations