🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
02457
CAS Number:
201532-42-5
Fmoc-β-(2-thiényl)-D-alanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Ala-3-(2-thiényl)-OH, ( R - N -Fmoc-2-thiénylalanine
Documents
$43.87 /1G
Taille
Request Bulk Quote
Product Information

Fmoc-b-(2-thienyl)-D-alanine 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, incorporating a thiophene ring, enhances the compound's ability to participate in various chemical reactions, making it a valuable building block in the design of bioactive peptides and pharmaceuticals. Researchers appreciate its stability and compatibility with a range of coupling reagents, which facilitates the efficient assembly of complex peptide sequences.

In addition to its role in peptide synthesis, Fmoc-b-(2-thienyl)-D-alanine has potential applications in the development of novel therapeutics targeting specific biological pathways. Its thiophene moiety may contribute to improved binding affinity and selectivity in drug design, particularly in the fields of oncology and neurology. The compound's unique properties make it an attractive choice for researchers looking to innovate in peptide-based drug discovery and development.

Synonyms
Fmoc-D-Ala-3-(2-thiényl)-OH, ( R - N -Fmoc-2-thiénylalanine
CAS Number
201532-42-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 22 H 19 NON 4 S
Molecular Weight
393.4
MDL Number
MFCD00065677
PubChem ID
7017917
Melting Point
164-173 °C
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-D-Ala-3-(2-thiényl)-OH, ( R - N -Fmoc-2-thiénylalanine
CAS Number
201532-42-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 22 H 19 NON 4 S
Molecular Weight
393.4
MDL Number
MFCD00065677
PubChem ID
7017917
Melting Point
164-173 °C
Appearance
Poudre blanche
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-b-(2-thienyl)-D-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids. It enhances the efficiency of creating complex peptides used in pharmaceuticals.
  • Drug Development: Its unique structure aids in the design of novel therapeutic agents, particularly in targeting specific biological pathways, making it valuable in the pharmaceutical industry.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems and diagnostic tools.
  • Research in Neuroscience: It plays a role in the study of neuropeptides, which are crucial for understanding various neurological disorders, thus contributing to advancements in treatments.
  • Material Science: The compound's properties can be exploited in creating functional materials, such as sensors and catalysts, benefiting industries focused on innovative material development.

Citations