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Catalog Number:
15532
CAS Number:
332062-10-9
Fmoc-4-phényl-D-β-homophénylalanine
Purity:
≥ 99 % (HPLC, pureté chirale)
Synonym(s):
Fmoc-D-β-HomoPhe(4-phényl)-OH, ( Acide R -Fmoc-3-amino-4,4-diphénylbutyrique
Documents
$154.93 /100 mg
Taille
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Product Information

Fmoc-4-phenyl-D-b-homophenylalanine 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 solid-phase peptide synthesis. Its unique structure, characterized by the presence of two phenyl groups, enhances its stability and solubility, making it an ideal choice for researchers looking to create complex peptides with improved bioactivity.

In the pharmaceutical industry, Fmoc-4-phenyl-D-b-homophenylalanine is particularly valuable for the synthesis of peptide-based therapeutics, including those targeting cancer and metabolic disorders. Its ability to facilitate the formation of diverse peptide sequences allows for the exploration of novel drug candidates. Additionally, this compound's favorable properties can lead to enhanced pharmacokinetics and bioavailability in therapeutic applications. Researchers and industry professionals will find Fmoc-4-phenyl-D-b-homophenylalanine to be a crucial building block in their quest for innovative peptide solutions.

Synonyms
Fmoc-D-β-HomoPhe(4-phényl)-OH, ( Acide R -Fmoc-3-amino-4,4-diphénylbutyrique
CAS Number
332062-10-9
Purity
≥ 99 % (HPLC, pureté chirale)
Molecular Formula
C 31 H 274
Molecular Weight
477.56
MDL Number
MFCD02094567
PubChem ID
53398013
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
Safety & Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
General Information
Synonyms
Fmoc-D-β-HomoPhe(4-phényl)-OH, ( Acide R -Fmoc-3-amino-4,4-diphénylbutyrique
CAS Number
332062-10-9
Purity
≥ 99 % (HPLC, pureté chirale)
Molecular Formula
C 31 H 274
Molecular Weight
477.56
MDL Number
MFCD02094567
PubChem ID
53398013
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
Safety & Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Properties
Additional property information coming soon!
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Applications

Fmoc-4-phenyl-D-b-homophenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing researchers to create complex peptide sequences efficiently.
  • Drug Development: It plays a significant role in the development of peptide-based therapeutics, offering potential treatments for various diseases, including cancer and metabolic disorders.
  • Bioconjugation: The chemical is used in bioconjugation processes to attach peptides to other biomolecules, enhancing the specificity and efficacy of drug delivery systems.
  • Research in Neuroscience: It is utilized in studies related to neuropeptides, helping researchers understand their role in neurotransmission and potential implications in neurological disorders.
  • Protein Engineering: The compound aids in the design of novel proteins with enhanced stability and functionality, which is crucial for applications in biotechnology and synthetic biology.

Citations