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CAS 501015-23-2

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3-[(tert-butoxycarbonyl)amino]-3-(2-nitrophenyl)propanoic acid

Description:
3-[(tert-butoxycarbonyl)amino]-3-(2-nitrophenyl)propanoic acid, with the CAS number 501015-23-2, is an organic compound characterized by its structure, which includes a propanoic acid backbone substituted with a tert-butoxycarbonyl (Boc) group and a 2-nitrophenyl moiety. The presence of the Boc group indicates that this compound is likely used as a protecting group for amines in synthetic chemistry, facilitating the selective functionalization of other reactive sites. The nitrophenyl group introduces electron-withdrawing characteristics, which can influence the compound's reactivity and solubility. This compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its functional groups suggest potential applications in medicinal chemistry, particularly in the design of bioactive molecules or as intermediates in the synthesis of pharmaceuticals. Additionally, the compound's stability and reactivity can be influenced by factors such as pH and temperature, making it important to consider these conditions in practical applications.
Formula:C14H18N2O6
InChI:InChI=1/C14H18N2O6/c1-14(2,3)22-13(19)15-10(8-12(17)18)9-6-4-5-7-11(9)16(20)21/h4-7,10H,8H2,1-3H3,(H,15,19)(H,17,18)
SMILES:CC(C)(C)OC(=NC(CC(=O)O)c1ccccc1N(=O)=O)O
Synonyms:
  • (3S)-3-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-(2-nitrophenyl)propanoic acid
  • benzenepropanoic acid, beta-[[(1,1-dimethylethoxy)carbonyl]amino]-2-nitro-, (betaS)-
  • Boc-(R)-3-Amino-3-(2-nitrophenyl)-propionic acid
  • Boc-(S)-3-Amino-3-(2-nitrophenyl)-propionic acid
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