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Catalog Number:
15252
CAS Number:
219967-74-5
Acide Fmoc-( S )-3-amino-5-phénylpentanoïque
Purity:
≥ 95%
Synonym(s):
Fmoc-Lb-Nva(5-phényl)-OH
Documents
$120.88 /250 mg
Taille
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Product Information

Fmoc-(S)-3-amino-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 not only enhances the stability of the amino acid but also facilitates the formation of complex peptide chains, making it an invaluable tool for researchers in the fields of biochemistry and medicinal chemistry.

In practical applications, Fmoc-(S)-3-amino-5-phenylpentanoic acid is particularly beneficial in the development of pharmaceuticals, where precise control over peptide sequences is crucial. Its ability to improve the yield and purity of synthesized peptides makes it a preferred choice among professionals. Additionally, the compound's compatibility with various coupling reagents and its ease of removal under mild conditions further enhance its appeal in laboratory settings. Researchers can leverage this compound to streamline their workflows and achieve high-quality results in peptide synthesis.

Synonyms
Fmoc-Lb-Nva(5-phényl)-OH
CAS Number
219967-74-5
Purity
≥ 95%
Molecular Formula
C 26 H 254
Molecular Weight
415.49
MDL Number
MFCD01861029
PubChem ID
17039472
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8°C
General Information
Synonyms
Fmoc-Lb-Nva(5-phényl)-OH
CAS Number
219967-74-5
Purity
≥ 95%
Molecular Formula
C 26 H 254
Molecular Weight
415.49
MDL Number
MFCD01861029
PubChem ID
17039472
Appearance
Poudre blanche à blanc cassé
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

Fmoc-(S)-3-amino-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, allowing researchers to create specific sequences for studies in biochemistry and pharmacology.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in the development of drugs targeting neurological disorders, enhancing therapeutic efficacy.
  • Protein Engineering: Used in the modification of proteins, it helps in creating variants with improved stability and functionality, which is crucial for industrial enzyme applications.
  • Bioconjugation: This chemical is valuable in bioconjugation techniques, linking biomolecules for targeted drug delivery systems, improving treatment precision in cancer therapies.
  • Research in Material Science: Its properties are explored in the development of new materials, such as hydrogels, which have applications in tissue engineering and regenerative medicine.

Citations