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Catalog Number:
07349
CAS Number:
159610-82-9
Fmoc-3-styryl-L-alanine
Purity:
≥ 98%
Synonym(s):
Fmoc-L-Ala(styryl)-OH, (S-2-(Fmoc-amino)-5-phenyl-4-pentenoic acid, Fmoc-Ala(styryl)-OH
Documents
$75.00 /250MG
Pack Size Availability Price
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Product Information

Fmoc-3-styryl-L-alanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique styryl group that enhances its reactivity and solubility, making it an excellent choice for researchers focused on developing novel peptides and therapeutic agents. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains, facilitating the synthesis of complex structures with high purity.

In the pharmaceutical industry, Fmoc-3-styryl-L-alanine is particularly valuable for creating bioactive peptides that can serve as potential drug candidates. Its ability to form stable interactions with biological targets positions it as a key component in the design of new therapeutics, especially in the fields of oncology and neurology. Researchers appreciate its compatibility with various coupling reagents and its efficiency in solid-phase peptide synthesis, making it a preferred choice for those aiming to streamline their workflows while achieving high-quality results.

Synonyms
Fmoc-L-Ala(styryl)-OH, (S-2-(Fmoc-amino)-5-phenyl-4-pentenoic acid, Fmoc-Ala(styryl)-OH
CAS Number
159610-82-9
Purity
≥ 98%
Molecular Formula
C26H23NO4
Molecular Weight
413.48
MDL Number
MFCD01311748
PubChem ID
4395787
Appearance
White to off-white powder
Optical Rotation
[a]D20 = +17 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Ala(styryl)-OH, (S-2-(Fmoc-amino)-5-phenyl-4-pentenoic acid, Fmoc-Ala(styryl)-OH
CAS Number
159610-82-9
Purity
≥ 98%
Molecular Formula
C26H23NO4
Molecular Weight
413.48
MDL Number
MFCD01311748
PubChem ID
4395787
Appearance
White to off-white powder
Optical Rotation
[a]D20 = +17 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-3-styryl-L-alanine 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, where its Fmoc protecting group allows for selective deprotection and coupling.
  • Drug Development: Researchers leverage its unique structure to design and develop novel therapeutic agents, especially in the field of cancer treatment, where targeting specific pathways can enhance efficacy.
  • Bioconjugation: Fmoc-3-styryl-L-alanine is used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, improving the functionality of drug delivery systems.
  • Fluorescent Probes: Its styryl group can be utilized in the development of fluorescent probes for imaging applications, enabling researchers to visualize cellular processes in real-time.
  • Material Science: This compound finds applications in the creation of functionalized polymers, enhancing material properties for applications in coatings and adhesives.

Citations