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Catalog Number:
03741
CAS Number:
198542-01-7
Ácido Fmoc-(3 S ,4 S -4-amino-3-hidroxi-5-fenilpentanoico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-AHPPA-OH
Documents
$127.79 /100 mg
Tamaño
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Product Information

Fmoc-(3S,4S)-4-amino-3-hydroxy-5-phenylpentanoic acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by a hydroxyl and phenyl group, enhances its solubility and reactivity, making it an excellent choice for researchers focused on developing complex peptide sequences.

In the pharmaceutical industry, this compound is particularly valuable for its role in the synthesis of bioactive peptides, which can serve as potential therapeutics for various diseases. Its ability to facilitate the formation of peptide bonds while maintaining stability under various conditions makes it a preferred choice among chemists. Additionally, the compound's specific stereochemistry contributes to its effectiveness in biological applications, ensuring that synthesized peptides exhibit the desired activity. Researchers and professionals can leverage this compound to streamline their synthesis processes and enhance the efficacy of their peptide-based products.

Synonyms
Fmoc-AHPPA-OH
CAS Number
198542-01-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C26H25Nº 5
Molecular Weight
431.5
MDL Number
MFCD00155625
PubChem ID
4712558
Appearance
Polvo amorfo blanco
Optical Rotation
[a] D 20 = -57 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-AHPPA-OH
CAS Number
198542-01-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C26H25Nº 5
Molecular Weight
431.5
MDL Number
MFCD00155625
PubChem ID
4712558
Appearance
Polvo amorfo blanco
Optical Rotation
[a] D 20 = -57 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(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 solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently.
  • Drug Development: Its unique structure can be modified to develop new pharmaceutical agents, particularly in the field of neuropharmacology.
  • Bioconjugation: The Fmoc group facilitates the attachment of biomolecules, enhancing the development of targeted drug delivery systems.
  • Protein Engineering: It is used in the modification of proteins, aiding in the design of proteins with enhanced stability and activity for therapeutic applications.
  • Research in Neuroscience: The compound's properties make it valuable in studying neurotransmitter systems, potentially leading to breakthroughs in treating neurological disorders.

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