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Catalog Number:
15614
CAS Number:
499995-73-2
Acide boc-( S -3-amino-3-(4-nitrophényl)propionique)
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-β-Phe(4-NO2)-OH, ( S -Boc-4-nitro-β-phénylalanine
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$58.39 /100 mg
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Product Information

Boc-(S)-3-amino-3-(4-nitrophenyl)propionic acid is a versatile compound widely utilized in the fields of medicinal chemistry and pharmaceutical research. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal candidate for peptide synthesis and drug development. Its unique structure, characterized by the presence of a nitrophenyl group, allows for specific interactions in biological systems, facilitating the design of targeted therapies and novel drug candidates.

Researchers have effectively employed Boc-(S)-3-amino-3-(4-nitrophenyl)propionic acid in the synthesis of bioactive peptides, contributing to advancements in therapeutic agents for various diseases. Its ability to act as a building block in complex organic synthesis further underscores its relevance in developing innovative solutions in the pharmaceutical industry. With its favorable properties and applications, this compound stands out as a valuable resource for professionals seeking to enhance their research and development efforts.

Synonyms
Boc-L-β-Phe(4-NO2)-OH, ( S -Boc-4-nitro-β-phénylalanine
CAS Number
499995-73-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C14H18N2O6
Molecular Weight
310.31
MDL Number
MFCD03427894
PubChem ID
3786935
Melting Point
132-138 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 25 = -40 ± 3º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-L-β-Phe(4-NO2)-OH, ( S -Boc-4-nitro-β-phénylalanine
CAS Number
499995-73-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C14H18N2O6
Molecular Weight
310.31
MDL Number
MFCD03427894
PubChem ID
3786935
Melting Point
132-138 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 25 = -40 ± 3º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-(S)-3-amino-3-(4-nitrophenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in creating modified amino acids that enhance the stability and activity of therapeutic peptides.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for the development of new drugs, especially those targeting specific biological pathways, due to its unique structural properties.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to drugs or imaging agents, improving targeting and efficacy in treatments.
  • Research in Neuroscience: Its derivatives are studied for their potential effects on neurotransmitter systems, making it valuable in the development of treatments for neurological disorders.
  • Analytical Chemistry: This chemical is employed in various analytical methods, including chromatography and mass spectrometry, to help identify and quantify complex mixtures in biological samples.

Citations