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Catalog Number:
07378
CAS Number:
119434-75-2
Boc-3-(4-thiazolyl)-L-alanine
Purity:
≥ 98% (HPLC, Chiral purity)
Synonym(s):
Boc-L-Ala(4-thiazoyl)-OH, (S-N-Boc-4-thiazoylalanine
Documents
$134.70 /1G
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Product Information

Boc-3-(4-thiazolyl)-L-alanine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its unique thiazole ring structure contributes to its potential as a building block for bioactive peptides, allowing for the exploration of novel therapeutic agents targeting various biological pathways.

In practical applications, Boc-3-(4-thiazolyl)-L-alanine can be utilized in the synthesis of peptide-based drugs, particularly those aimed at treating infectious diseases or cancer, due to its ability to mimic natural amino acids while providing enhanced properties. Additionally, its compatibility with various coupling reagents and methodologies makes it a preferred choice for chemists looking to streamline their synthesis processes. With its promising applications and unique structural features, this compound stands out as a valuable asset in pharmaceutical research and development.

Synonyms
Boc-L-Ala(4-thiazoyl)-OH, (S-N-Boc-4-thiazoylalanine
CAS Number
119434-75-2
Purity
≥ 98% (HPLC, Chiral purity)
Molecular Formula
C11H16N2O4S
Molecular Weight
272.32
MDL Number
MFCD00079682
PubChem ID
14540322
Appearance
White to pale yellow powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-Ala(4-thiazoyl)-OH, (S-N-Boc-4-thiazoylalanine
CAS Number
119434-75-2
Purity
≥ 98% (HPLC, Chiral purity)
Molecular Formula
C11H16N2O4S
Molecular Weight
272.32
MDL Number
MFCD00079682
PubChem ID
14540322
Appearance
White to pale yellow powder
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

Boc-3-(4-thiazolyl)-L-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 without affecting others. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: Its thiazole ring structure contributes to the biological activity of compounds, making it valuable in the design of new drugs, particularly in targeting specific diseases like cancer or infections.
  • Biochemical Research: Researchers use this compound to study protein interactions and enzyme activities, helping to elucidate mechanisms of action in various biological pathways.
  • Diagnostic Applications: The compound can be used in the development of diagnostic tools, particularly in assays that require specific binding interactions, enhancing the sensitivity and specificity of tests.
  • Material Science: Its unique properties allow for applications in creating novel materials with specific functionalities, such as drug delivery systems that can release therapeutics in a controlled manner.

Citations