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Catalog Number:
07322
CAS Number:
269078-74-2
Acide Fmoc-( R -4-amino-5-phénylpentanoïque
Purity:
≥ 99 % (HPLC)
Synonym(s):
( Acide R -4-(Fmoc-amino)-5-phénylvalérique, Fmoc-γ-L-dihomophénylalanine
Documents
$127.79 /100 mg
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Product Information

Fmoc-(R)-4-amino-5-phenylpentanoic acid is a versatile building block 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 allows for efficient coupling reactions, making it an ideal choice for researchers focused on developing complex peptide sequences. The (R) configuration enhances its bioactivity, making it particularly relevant in pharmaceutical applications where chirality plays a crucial role in efficacy.

In addition to its primary use in peptide synthesis, Fmoc-(R)-4-amino-5-phenylpentanoic acid can also serve as a valuable intermediate in the production of various bioactive compounds. Its stability and compatibility with standard coupling reagents make it a preferred option for chemists in both academic and industrial settings. Researchers can leverage this compound to streamline their workflows, enhance yields, and achieve high purity in their final products, ultimately accelerating the pace of discovery in drug development and related fields.

Synonyms
( Acide R -4-(Fmoc-amino)-5-phénylvalérique, Fmoc-γ-L-dihomophénylalanine
CAS Number
269078-74-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 26 H 254
Molecular Weight
415.49
MDL Number
MFCD01074522
PubChem ID
4712580
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -23 ± 1 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
( Acide R -4-(Fmoc-amino)-5-phénylvalérique, Fmoc-γ-L-dihomophénylalanine
CAS Number
269078-74-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 26 H 254
Molecular Weight
415.49
MDL Number
MFCD01074522
PubChem ID
4712580
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -23 ± 1 ° (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

Fmoc-(R)-4-amino-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 with high purity and yield.
  • Drug Development: Its structural properties make it valuable in the design of peptide-based pharmaceuticals, particularly in targeting specific biological pathways.
  • Bioconjugation: The Fmoc group facilitates the attachment of peptides to various biomolecules, enhancing the development of targeted drug delivery systems.
  • Research in Neuroscience: This compound is used in studies investigating neuropeptides, contributing to the understanding of neurological functions and disorders.
  • Custom Synthesis Services: Many chemical suppliers offer tailored synthesis of this compound, catering to specific research needs in academic and industrial laboratories.

Citations