Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
02723
CAS Number:
33305-77-0
Boc-4-nitro-L-phenylalanine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-Phe(4-NO2)-OH, Boc-p-nitro-L-Phe-OH, Boc-Phe(4-NO2)-OH
Documents
$18.53 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-4-nitro-L-phenylalanine is a versatile amino acid derivative widely utilized 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 nitro group not only contributes to its reactivity but also allows for specific modifications that can be leveraged in various biochemical applications.

In the pharmaceutical industry, Boc-4-nitro-L-phenylalanine serves as a crucial building block for the synthesis of bioactive peptides, which are essential in developing therapeutics for a range of diseases. Its applications extend to the fields of medicinal chemistry and biochemistry, where it is employed in the design of novel compounds with enhanced biological activity. Researchers appreciate its ability to facilitate the introduction of functional groups, thereby expanding the potential for creating innovative drug candidates.

Synonyms
Boc-L-Phe(4-NO2)-OH, Boc-p-nitro-L-Phe-OH, Boc-Phe(4-NO2)-OH
CAS Number
33305-77-0
Purity
≥ 99% (HPLC)
Molecular Formula
C14H18N2O6
Molecular Weight
310.3
MDL Number
MFCD00038128
PubChem ID
118071
Appearance
Faintly yellow powder
Optical Rotation
[a]D20 = +8 ± 1º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-Phe(4-NO2)-OH, Boc-p-nitro-L-Phe-OH, Boc-Phe(4-NO2)-OH
CAS Number
33305-77-0
Purity
≥ 99% (HPLC)
Molecular Formula
C14H18N2O6
Molecular Weight
310.3
MDL Number
MFCD00038128
PubChem ID
118071
Appearance
Faintly yellow powder
Optical Rotation
[a]D20 = +8 ± 1º (C=1 in MeOH)
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-4-nitro-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing chemists to selectively modify amino acids without affecting others, which is crucial for creating complex biomolecules.
  • Drug Development: Its unique properties make it a valuable intermediate in the development of pharmaceuticals, particularly in designing compounds that target specific biological pathways.
  • Bioconjugation: The nitro group can be used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: This compound can be employed in studies investigating neurotransmitter pathways, helping researchers understand the role of amino acids in brain function and disorders.
  • Analytical Chemistry: It is used as a standard in analytical methods to quantify amino acids in various samples, providing reliable data for researchers in food science and biochemistry.

Citations