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Catalog Number:
15659
CAS Number:
499995-80-1
Acide boc-( S )-3-amino-3-(4-hydroxyphényl)propionique
Purity:
≥ 96 % (HPLC)
Synonym(s):
Boc-L-β-Phe(4-OH)-OH, Boc-L-β-Tyr-OH
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$70.00 /100 mg
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Product Information

Boc-(S)-3-amino-3-(4-hydroxyphenyl)propionic acid is a versatile compound widely utilized in pharmaceutical and biochemical 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 4-hydroxyphenyl group, allows for specific interactions in biological systems, facilitating studies in enzyme inhibition and receptor binding.

Researchers often employ Boc-(S)-3-amino-3-(4-hydroxyphenyl)propionic acid in the synthesis of bioactive peptides and as a building block in the development of novel therapeutic agents. Its application extends to the design of compounds targeting various biological pathways, particularly in the fields of neuropharmacology and cancer research. The compound's favorable properties, such as its ease of modification and compatibility with various coupling reactions, make it a valuable tool for professionals seeking to innovate in drug discovery and development.

Synonyms
Boc-L-β-Phe(4-OH)-OH, Boc-L-β-Tyr-OH
CAS Number
499995-80-1
Purity
≥ 96 % (HPLC)
Molecular Formula
C 14 H 195
Molecular Weight
281.31
MDL Number
MFCD03427903
PubChem ID
2764539
Melting Point
152 - 158 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = -48 à -58º (C=1 dans EtOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-L-β-Phe(4-OH)-OH, Boc-L-β-Tyr-OH
CAS Number
499995-80-1
Purity
≥ 96 % (HPLC)
Molecular Formula
C 14 H 195
Molecular Weight
281.31
MDL Number
MFCD03427903
PubChem ID
2764539
Melting Point
152 - 158 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = -48 à -58º (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-(S)-3-amino-3-(4-hydroxyphenyl)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 those that require specific stereochemistry for biological activity, enhancing the effectiveness of drug development.
  • Drug Development: Its unique structure allows for the design of novel pharmaceuticals targeting various diseases, especially in oncology and neurology, where precise molecular interactions are crucial.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to therapeutic agents, which improves drug delivery and efficacy in targeted therapies.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems due to its structural similarity to amino acids, aiding in the development of treatments for neurological disorders.
  • Cosmetic Formulations: Its antioxidant properties make it valuable in cosmetic formulations, helping to protect skin from oxidative stress and improve overall skin health.

Citations