Fmoc-L-2-(2-Thienyl)glycine is a synthetic amino acid derivative commonly used in peptide synthesis and research. It features a phenylmethoxycarbonyl (Fmoc) protecting group, which is widely employed to protect the amino group during peptide assembly. The presence of the thienyl group, a five-membered aromatic ring containing sulfur, contributes unique electronic and steric properties, enhancing the compound's potential in various biochemical applications. This compound is typically characterized by its solid-state form, exhibiting stability under standard laboratory conditions. Its solubility is generally moderate in organic solvents, which facilitates its use in organic synthesis. The compound's structure allows for specific interactions in biological systems, making it valuable in the development of peptide-based drugs and materials. Additionally, Fmoc-L-2-(2-Thienyl)glycine can be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its identity and purity. Overall, this compound serves as a versatile building block in the field of medicinal chemistry and peptide research.

Fmoc-L-2-(2-Thienyl)glycine

208259-66-9: Fmoc-L-2-(2-Thienyl)glycine is a synthetic amino acid derivative commonly used in peptide synthesis and research. It features a phenylmethoxycarbonyl (Fmoc) protecting group, which is widely employed to protect the amino group during peptide assembly. The presence of the thienyl group, a five-membered aromatic ring containing sulfur, contributes unique electronic and steric properties, enhancing the compound's potential in various biochemical applications. This compound is typically characterized by its solid-state form, exhibiting stability under standard laboratory conditions. Its solubility is generally moderate in organic solvents, which facilitates its use in organic synthesis. The compound's structure allows for specific interactions in biological systems, making it valuable in the development of peptide-based drugs and materials. Additionally, Fmoc-L-2-(2-Thienyl)glycine can be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its identity and purity. Overall, this compound serves as a versatile building block in the field of medicinal chemistry and peptide research.

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

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

CAS 208259-66-9

Fmoc-L-2-(2-Thienyl)glycine

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

Ref: IN-DA002JLE

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

Ref: 54-OR80929

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

Ref: 10-F241385