(S)-2-(tert-butoxycarbonylamino)-3-(thiophen-2-yl)propanoic acid
$350.00
CAS No.: 56675-37-7
Catalog No.: 196091
Purity: 95%
MF: C12H17NO4S
MW: 271.338
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OC(=O)N[C@H](C(=O)O)CC=1SC=CC1
Catalog No.: 196091
Purity: 95%
MF: C12H17NO4S
MW: 271.338
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OC(=O)N[C@H](C(=O)O)CC=1SC=CC1
CAS NO.: 56675-37-7; (S)-2-(tert-butoxycarbonylamino)-3-(thiophen-2-yl)propanoic acid. PROPERTIES: (S)-2-(tert-butoxycarbonylamino)-3-(thiophen-2-yl)propanoic acid is a crystalline powder with a molecular weight of approximately 286.3 g/mol. It has a melting point between 120-125°C. The compound is moderately soluble in polar organic solvents like dimethylformamide and methanol but has limited water solubility. The tert-butoxycarbonyl group protects the amine functionality. For proper storage, keep in a tightly sealed container at room temperature away from moisture. Safety: This compound may cause respiratory sensitization. In case of exposure to large quantities, provide rest and fresh air. Use explosion-proof ventilation and lighting if handling large quantities. APPLICATIONS: In peptide synthesis, (S)-2-(tert-butoxycarbonylamino)-3-(thiophen-2-yl)propanoic acid serves as a protected amino acid building block. The Boc group protects the amine during coupling reactions. In pharmaceutical research, it is used to create bioactive peptides with specific conformational constraints. The thiophene ring provides structural features that enhance binding to biological targets. In materials science, derivatives of this compound are explored for creating molecular recognition elements. The combination of the thiophene ring and the carboxylic acid group creates a scaffold that can selectively bind certain analytes. These applications are documented in peptide chemistry journals and materials science research articles.
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