(R)-N-FMOC-2-Thienylalanine is a synthetic amino acid derivative characterized by the presence of a thienyl group, which is a five-membered aromatic ring containing sulfur. The "FMOC" (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino functionality, commonly used in peptide synthesis to prevent unwanted reactions during the coupling process. This compound is typically utilized in the field of organic chemistry and biochemistry, particularly in the synthesis of peptides and proteins. Its chirality, indicated by the "(R)" designation, suggests that it has specific stereochemical properties that can influence the biological activity and interactions of the resulting peptides. The presence of the thienyl moiety may also impart unique electronic and steric properties, making it an interesting candidate for various applications in medicinal chemistry and drug design. Overall, (R)-N-FMOC-2-Thienylalanine is valued for its utility in synthesizing complex biomolecules while maintaining the integrity of the amino acid structure.

(R)-N-FMOC-2-Thienylalanine

201532-42-5: Fmoc-.beta.-(2-thienyl)-D-Ala-OH, N-(9-Fluorenylmethoxycarbonyl)-2-thienyl-D-alanine, Fmoc-D-2-Thienylalanine, Fmoc-D-3-(2-Thienyl)-alanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3-thiophen-2-yl-D-alanine, (2R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-thiophen-2-ylpropanoate, Fmoc-3-(2-Thienyl)-D-alanine

3-(Thien-2-yl)-D-alanine, N-FMOC protected

CAS 201532-42-5: (R)-N-FMOC-2-Thienylalanine

3-(Thien-2-yl)-D-alanine, N-FMOC protected

Ref: 54-OR14645

(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(thiophen-2-yl)propanoic acid

Ref: 10-F463595

N-Fmoc-D-Thienylalanine (Fmoc-D-Thi-OH)

Ref: 4Z-T-449002

2-Thiophenepropanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αR)-

Ref: IN-DA002DH3