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Catalog Number:
15203
CAS Number:
127106-71-2
Boc-4-nitro-L-β-homophénylalanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-β-HomoPhe(4-NO2)-OH, Acide boc-( S -3-amino-4-(4-nitrophényl)butyrique)
Documents
$120.88 /250 mg
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Product Information

Boc-4-nitro-L-b-homophenylalanine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its unique nitro group provides additional functionalization opportunities, allowing for the development of novel therapeutic agents.

In practical applications, Boc-4-nitro-L-b-homophenylalanine is utilized in the synthesis of peptides that target specific biological pathways, contributing to advancements in drug discovery and development. This compound is particularly valuable in the creation of peptide-based therapeutics, where its structural properties can be leveraged to improve efficacy and selectivity. Researchers appreciate its compatibility with various coupling reactions, making it a preferred choice for complex peptide assembly. With its robust profile, Boc-4-nitro-L-b-homophenylalanine stands out as a key building block for innovative pharmaceutical applications.

Synonyms
Boc-L-β-HomoPhe(4-NO2)-OH, Acide boc-( S -3-amino-4-(4-nitrophényl)butyrique)
CAS Number
127106-71-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C15H20N2O6
Molecular Weight
324.33
MDL Number
MFCD01076286
PubChem ID
14769462
Appearance
Poudre blanche
Optical Rotation
[α] D 25 = -22,0 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Boc-L-β-HomoPhe(4-NO2)-OH, Acide boc-( S -3-amino-4-(4-nitrophényl)butyrique)
CAS Number
127106-71-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C15H20N2O6
Molecular Weight
324.33
MDL Number
MFCD01076286
PubChem ID
14769462
Appearance
Poudre blanche
Optical Rotation
[α] D 25 = -22,0 ± 2º (C=1 dans EtOH)
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-4-nitro-L-b-homophenylalanine 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 novel therapeutic agents. Its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In pharmaceutical research, it is used to create compounds with potential anti-cancer properties. The nitro group can be modified to improve biological activity, making it a key player in drug discovery.
  • Bioconjugation: The compound is employed in bioconjugation processes, where it can be linked to other biomolecules. This application is crucial in creating targeted drug delivery systems, improving the efficacy of treatments.
  • Research on Amino Acid Analogues: It is used to study the effects of amino acid modifications on protein function and stability, providing insights into enzyme mechanisms and protein interactions.
  • Material Science: In the field of material science, Boc-4-nitro-L-b-homophenylalanine is explored for its potential in developing new materials with specific properties, such as enhanced biocompatibility for medical devices.

Citations