🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
02559
CAS Number:
72155-48-7
Acide boc-(3 S ,4 S )-4-amino-3-hydroxy-5-phénylpentanoïque
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-AHPPA-OH
Documents
$86.23 /25 mg
Taille
Request Bulk Quote
Product Information

Boc-(3S,4S)-4-amino-3-hydroxy-5-phenylpentanoic acid is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound, also known as Boc-4-amino-3-hydroxy-5-phenylpentanoic acid, features a Boc (tert-butyloxycarbonyl) protecting group that enhances its stability and solubility, making it an ideal choice for researchers focusing on complex peptide structures. Its unique stereochemistry (3S,4S) contributes to its specificity in biological applications, particularly in the development of therapeutics targeting various diseases.

The practical applications of Boc-(3S,4S)-4-amino-3-hydroxy-5-phenylpentanoic acid extend to the synthesis of bioactive peptides and drug candidates, where it serves as a crucial building block. Its ability to facilitate selective reactions and improve the yield of desired products makes it a valuable asset in medicinal chemistry and biochemistry. Researchers can leverage this compound to explore innovative solutions in drug design, enhancing the efficacy and safety profiles of new therapeutic agents.

Synonyms
Boc-AHPPA-OH
CAS Number
72155-48-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 16 H 235
Molecular Weight
309.4
MDL Number
MFCD00065553
Appearance
Poudre amorphe blanche
Optical Rotation
[a] D = -34 ± 2° (C=1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-AHPPA-OH
CAS Number
72155-48-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 16 H 235
Molecular Weight
309.4
MDL Number
MFCD00065553
Appearance
Poudre amorphe blanche
Optical Rotation
[a] D = -34 ± 2° (C=1 dans DMF)
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-(3S,4S)-4-amino-3-hydroxy-5-phenylpentanoic 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 the pharmaceutical industry, where it helps create biologically active compounds.
  • Drug Development: It plays a significant role in developing new drugs, especially in designing molecules that can interact effectively with biological targets, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach drugs or imaging agents to biomolecules, improving targeted delivery systems in cancer therapy.
  • Research in Neuroscience: It is valuable in studying neuroactive peptides, contributing to advancements in understanding neurological disorders and potential treatments.
  • Custom Synthesis Services: Many chemical suppliers offer custom synthesis of this compound, catering to specific research needs, which is beneficial for labs requiring tailored solutions.

Citations