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CAS 53030-49-2

:

3-[(tert-butoxycarbonyl)amino]-3-thiophen-2-ylpropanoic acid

Description:
3-[(tert-butoxycarbonyl)amino]-3-thiophen-2-ylpropanoic acid, with the CAS number 53030-49-2, is an organic compound characterized by its unique structure that includes a thiophene ring, a propanoic acid moiety, and a tert-butoxycarbonyl (Boc) protecting group on the amino functional group. This compound typically appears as a solid and is soluble in polar organic solvents. The presence of the thiophene ring contributes to its aromatic properties, while the Boc group serves as a protective group for the amine, making it useful in peptide synthesis and other organic reactions. The carboxylic acid functionality allows for potential reactivity in various chemical transformations, including esterification and amidation. Additionally, the compound may exhibit biological activity, making it of interest in pharmaceutical research. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its handling and application in synthetic chemistry.
Formula:C12H17NO4S
InChI:InChI=1/C12H17NO4S/c1-12(2,3)17-11(16)13-8(7-10(14)15)9-5-4-6-18-9/h4-6,8H,7H2,1-3H3,(H,13,16)(H,14,15)
SMILES:CC(C)(C)OC(=NC(CC(=O)O)c1cccs1)O
Synonyms:
  • (3S)-3-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-(2-thienyl)propanoic acid
  • 2-Thiophenepropanoic Acid, Beta-[[(1,1-Dimethylethoxy)Carbonyl]Amino]-
  • 2-thiophenepropanoic acid, beta-[[(1,1-dimethylethoxy)carbonyl]amino]-, (betaS)-
  • 3-[(tert-Butoxycarbonyl)amino]-3-(2-thienyl)propanoic acid
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