Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
07379
CAS Number:
134107-69-0
Boc-3-(4-tiazolil)-D-alanina
Purity:
≥ 99% (pureza quiral)
Synonym(s):
Boc-D-Ala(4-tiazoil)-OH, ( R - N -Boc-4-tiazoilalanina
Documents
$70.50 /250 mg
Tamaño
Request Bulk Quote
Product Information

Boc-3-(4-thiazolyl)-D-alanine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is characterized by its unique thiazole ring, which enhances its biological activity and stability, making it an attractive candidate for researchers in medicinal chemistry. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective reactions, facilitating the synthesis of complex peptides and bioactive molecules.

In pharmaceutical applications, Boc-3-(4-thiazolyl)-D-alanine is utilized in the design of novel therapeutics, particularly in the development of inhibitors and modulators targeting various biological pathways. Its structural properties enable it to interact effectively with biological systems, which is essential for drug efficacy. Additionally, this compound is valuable in the study of protein interactions and enzyme mechanisms, providing insights that can lead to innovative treatments. Researchers and industry professionals will find Boc-3-(4-thiazolyl)-D-alanine to be a key building block in their pursuit of advanced biochemical applications.

Synonyms
Boc-D-Ala(4-tiazoil)-OH, ( R - N -Boc-4-tiazoilalanina
CAS Number
134107-69-0
Purity
≥ 99% (pureza quiral)
Molecular Formula
C11H16N2O4S
Molecular Weight
272.32
MDL Number
MFCD00079680
PubChem ID
14540322
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-D-Ala(4-tiazoil)-OH, ( R - N -Boc-4-tiazoilalanina
CAS Number
134107-69-0
Purity
≥ 99% (pureza quiral)
Molecular Formula
C11H16N2O4S
Molecular Weight
272.32
MDL Number
MFCD00079680
PubChem ID
14540322
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-3-(4-thiazolyl)-D-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require thiazole-containing residues, enhancing the diversity of peptide libraries for drug discovery.
  • Pharmaceutical Development: Its unique structure allows for the development of novel therapeutics, especially in targeting specific biological pathways, making it valuable in the pharmaceutical industry.
  • Biochemical Research: Researchers use it to study protein interactions and enzyme activities, providing insights into metabolic pathways and potential drug targets.
  • Analytical Chemistry: The compound can be utilized in the development of analytical methods for detecting and quantifying thiazole derivatives, aiding in quality control processes in various industries.
  • Cosmetic Formulations: Its properties may be explored in cosmetic chemistry for formulating products that promote skin health, leveraging its biochemical activity.

Citas