(S)-N-BOC-4-Thiazoylalanine is a synthetic amino acid derivative characterized by the presence of a thiazole ring and a tert-butyloxycarbonyl (BOC) protecting group. This compound features a chiral center, which contributes to its stereochemistry, specifically the (S) configuration. The BOC group serves as a protective moiety for the amino group, facilitating its use in peptide synthesis by preventing unwanted reactions during coupling processes. The thiazole moiety introduces unique electronic and steric properties, which can influence the compound's reactivity and interactions in biological systems. This substance is typically utilized in the field of medicinal chemistry and peptide synthesis, where it can serve as a building block for more complex molecules. Its solubility and stability are influenced by the presence of the BOC group and the thiazole ring, making it suitable for various synthetic applications. As with many amino acid derivatives, careful handling and storage are recommended to maintain its integrity and prevent degradation.

(S)-N-BOC-4-Thiazoylalanine

119434-75-2: Boc-L-4-Thiazolylalanine, Boc-L-4-Thiazoylalanine, Boc-3-(4-Thiazolyl)-L-Alanine

Boc-3-(4-thiazolyl)-L-alanine is a synthetic compound that is synthesized from 4-thiazolium chloride and L-alanine. It can be easily tracked, extracted, and synthesized efficiently.

Boc-3-(4-thiazolyl)-L-alanine

Boc-β-(4-thiazolyl)-Ala-OH

3-Thiazol-4-yl-L-alanine, N-BOC protected

CAS 119434-75-2: (S)-N-BOC-4-Thiazoylalanine

Boc-3-(4-thiazolyl)-L-alanine

Ref: 3D-FB49180

Boc-β-(4-thiazolyl)-Ala-OH

Ref: 7W-GM4249

3-Thiazol-4-yl-L-alanine, N-BOC protected

Ref: 54-OR14634

(S)-2-((tert-Butoxycarbonyl)amino)-3-(thiazol-4-yl)propanoic acid

Ref: 10-F241369

4-Thiazolepropanoic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (αS)-

Ref: IN-DA000IRQ