🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
07380
CAS Number:
205528-32-1
Fmoc-3-(4-thiazolyl)-L-alanine
Purity:
≥ 99% (Chiral HPLC, HPLC)
Synonym(s):
Fmoc-L-Ala(4-thiazoyl)-OH, (S)-N-Fmoc-4-thiazoylalanine
Documents
$30.00 /250MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-3-(4-thiazolyl)-L-alanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis of peptides, making it an essential building block in the field of medicinal chemistry. Its unique thiazole side chain enhances the compound's biological activity, providing researchers with a valuable tool for designing peptides with improved pharmacological properties.

In addition to its role in peptide synthesis, Fmoc-3-(4-thiazolyl)-L-alanine has shown potential in various applications, including the development of novel therapeutics targeting specific biological pathways. Its stability and compatibility with standard coupling reagents make it an ideal choice for researchers looking to streamline their synthesis processes. With its ability to enhance peptide stability and activity, this compound is particularly relevant for those working in drug discovery and development, offering a pathway to innovative solutions in the pharmaceutical industry.

Synonyms
Fmoc-L-Ala(4-thiazoyl)-OH, (S)-N-Fmoc-4-thiazoylalanine
CAS Number
205528-32-1
Purity
≥ 99% (Chiral HPLC, HPLC)
Molecular Formula
C21H18N2O4S
Molecular Weight
394.45
MDL Number
MFCD00672568
PubChem ID
53394997
Melting Point
178 - 181 °C
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Ala(4-thiazoyl)-OH, (S)-N-Fmoc-4-thiazoylalanine
CAS Number
205528-32-1
Purity
≥ 99% (Chiral HPLC, HPLC)
Molecular Formula
C21H18N2O4S
Molecular Weight
394.45
MDL Number
MFCD00672568
PubChem ID
53394997
Melting Point
178 - 181 °C
Appearance
White powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-3-(4-thiazolyl)-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 (SPPS), allowing for the creation of complex peptide sequences with high purity.
  • Drug Development: Its unique thiazole moiety enhances the biological activity of peptides, making it valuable in the pharmaceutical industry for developing new drugs targeting specific diseases.
  • Bioconjugation: The Fmoc protecting group enables selective reactions, facilitating the conjugation of peptides to various biomolecules, which is essential in creating targeted therapies and diagnostics.
  • Research in Protein Engineering: Researchers utilize this compound to modify proteins, improving their stability and functionality, which is crucial in fields like biotechnology and synthetic biology.
  • Analytical Chemistry: It can be employed as a standard in analytical techniques such as HPLC, aiding in the quantification and characterization of peptide samples in various studies.

Citations