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Catalog Number:
15452
CAS Number:
479064-97-6
Acide boc-( R -3-amino-3-(4-méthylphényl)propionique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-β-Phe(4-Me)-OH, ( R -Boc-4-méthyl-β-phénylalanine
Documents
$72.31 /100 mg
Taille
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Product Information

Boc-(R)-3-amino-3-(4-methylphenyl)propionic acid is a versatile amino acid derivative that plays a significant role in pharmaceutical and biochemical research. This compound is recognized for its unique structure, featuring a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an ideal candidate for peptide synthesis and drug development. Its chiral center allows for the exploration of enantiomer-specific biological activities, which is crucial in the design of targeted therapeutics.

Researchers and industry professionals utilize Boc-(R)-3-amino-3-(4-methylphenyl)propionic acid in the synthesis of bioactive peptides and as a building block in the development of novel pharmaceuticals. Its application extends to the fields of medicinal chemistry and biochemistry, where it aids in the creation of compounds with improved efficacy and reduced side effects. The compound's favorable properties, such as its ability to facilitate the formation of stable peptide bonds, make it a valuable asset in the advancement of drug discovery and development processes.

Synonyms
Boc-L-β-Phe(4-Me)-OH, ( R -Boc-4-méthyl-β-phénylalanine
CAS Number
479064-97-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C 15 H 214
Molecular Weight
279.34
MDL Number
MFCD03427935
PubChem ID
2756809
Melting Point
148-154 ºC
Appearance
Solide blanc
Optical Rotation
[a] D 25 = +49 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-L-β-Phe(4-Me)-OH, ( R -Boc-4-méthyl-β-phénylalanine
CAS Number
479064-97-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C 15 H 214
Molecular Weight
279.34
MDL Number
MFCD03427935
PubChem ID
2756809
Melting Point
148-154 ºC
Appearance
Solide blanc
Optical Rotation
[a] D 25 = +49 ± 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-(R)-3-amino-3-(4-methylphenyl)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 pharmaceutical research, allowing for the development of new therapeutic agents.
  • Drug Development: Its unique structure makes it valuable in the design of drugs targeting specific biological pathways, particularly in the field of oncology and neurology.
  • Bioconjugation: The compound can be used in bioconjugation processes, enabling the attachment of drugs to antibodies for targeted therapy, enhancing drug efficacy while minimizing side effects.
  • Research on Amino Acid Analogues: It aids in the study of amino acid analogues, providing insights into protein structure and function, which is crucial for biochemistry and molecular biology research.
  • Custom Synthesis: Researchers can utilize this compound for custom synthesis projects, allowing for tailored solutions in various applications, from material science to agrochemicals.

Citations