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CAS 500788-99-8

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3-[(tert-butoxycarbonyl)amino]-3-thiophen-3-ylpropanoic acid

Description:
3-[(tert-butoxycarbonyl)amino]-3-thiophen-3-ylpropanoic acid is an organic compound characterized by its unique structure, which includes a thiophene ring and a tert-butoxycarbonyl (Boc) protecting group attached to an amino group. This compound typically exhibits properties associated with both amino acids and thiophene derivatives, such as solubility in polar solvents and potential reactivity due to the presence of functional groups. The Boc group serves as a protective moiety, making the compound useful in peptide synthesis and other organic reactions where selective functionalization is required. The thiophene ring contributes to the compound's aromatic character and may influence its electronic properties, making it of interest in various applications, including pharmaceuticals and materials science. Additionally, the presence of a carboxylic acid group suggests potential for further derivatization or interaction in biological systems. Overall, this compound exemplifies the intersection of organic synthesis and functional group manipulation in the development of complex molecules.
Formula:C12H17NO4S
InChI:InChI=1/C12H17NO4S/c1-12(2,3)17-11(16)13-9(6-10(14)15)8-4-5-18-7-8/h4-5,7,9H,6H2,1-3H3,(H,13,16)(H,14,15)
SMILES:CC(C)(C)OC(=NC(CC(=O)O)c1ccsc1)O
Synonyms:
  • (3R)-3-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-(3-thienyl)propanoic acid
  • 3-thiophenepropanoic acid, beta-[[(1,1-dimethylethoxy)carbonyl]amino]-, (betaR)-
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