🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
16933
CAS Number:
852288-18-7
Fmoc-3,4-dihydroxy-L-phénylalanine, protégé par acétonide
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-DOPA-OH, protégé par acétonide, Fmoc-DOPA(acétonide)-OH
Documents
$60.00 /100 mg
Taille
Request Bulk Quote
Product Information

Fmoc-3,4-dihydroxy-L-phenylalanine, acetonide protected is a specialized amino acid derivative widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amino groups during solid-phase peptide synthesis. Its acetonide protection enhances stability and solubility, making it an ideal choice for researchers focused on developing complex peptides and proteins.

This compound is particularly valuable in the synthesis of bioactive peptides, which have applications in pharmaceuticals, biotechnology, and materials science. Its ability to facilitate the incorporation of hydroxyl groups into peptide chains allows for the creation of peptides with enhanced biological activity and specificity. Researchers can leverage Fmoc-3,4-dihydroxy-L-phenylalanine, acetonide protected to explore novel therapeutic agents, improve drug delivery systems, and develop advanced biomaterials, making it a versatile tool in both academic and industrial settings.

Synonyms
Fmoc-DOPA-OH, protégé par acétonide, Fmoc-DOPA(acétonide)-OH
CAS Number
852288-18-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 27 H 256
Molecular Weight
459.5
MDL Number
MFCD08064332
PubChem ID
68151072
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -26 ± 3 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-DOPA-OH, protégé par acétonide, Fmoc-DOPA(acétonide)-OH
CAS Number
852288-18-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 27 H 256
Molecular Weight
459.5
MDL Number
MFCD08064332
PubChem ID
68151072
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -26 ± 3 ° (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-3,4-dihydroxy-L-phenylalanine, acetonide protected 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 for the creation of complex and diverse peptide structures.
  • Drug Development: It is used in the development of pharmaceutical compounds, especially those targeting neurological disorders, due to its structural similarity to neurotransmitters.
  • Bioconjugation: The compound can be employed in bioconjugation processes, facilitating the attachment of biomolecules to therapeutic agents, enhancing their efficacy and specificity.
  • Research in Neuroscience: Its unique properties make it valuable in neuroscience research, particularly in studying the effects of modified amino acids on neuronal function and signaling pathways.
  • Cosmetic Formulations: The compound is also explored in cosmetic chemistry for its potential antioxidant properties, contributing to formulations aimed at skin health and anti-aging.

Citations