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CAS 221352-46-1

:

2-(1,1-Dimethylethyl) 1,3-dihydro-2H-isoindole-1,2-dicarboxylate

Description:
2-(1,1-Dimethylethyl) 1,3-dihydro-2H-isoindole-1,2-dicarboxylate, with the CAS number 221352-46-1, is a chemical compound characterized by its isoindole structure, which features a bicyclic system comprising a five-membered ring fused to a six-membered ring. This compound contains two carboxylate groups, contributing to its potential reactivity and solubility in polar solvents. The presence of the tert-butyl group (1,1-dimethylethyl) enhances its hydrophobic characteristics, which can influence its interactions in biological systems and its overall stability. Typically, compounds of this nature may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The dihydro form indicates that the compound may have reduced aromaticity compared to fully aromatic derivatives, which can affect its electronic properties and reactivity. Overall, this compound's unique structural features suggest potential applications in various fields, including pharmaceuticals and organic synthesis. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.
Formula:C14H17NO4
InChI:InChI=1S/C14H17NO4/c1-14(2,3)19-13(18)15-8-9-6-4-5-7-10(9)11(15)12(16)17/h4-7,11H,8H2,1-3H3,(H,16,17)
InChI key:InChIKey=BBMCBMREDOQCDU-UHFFFAOYSA-N
SMILES:C(O)(=O)C1C=2C(CN1C(OC(C)(C)C)=O)=CC=CC2
Synonyms:
  • 1,3-Dihydro-Isoindole-1,2-Dicarboxylic Acid 2-Tert-Butyl Ester
  • 2-(1,1-Dimethylethyl) 1,3-dihydro-2H-isoindole-1,2-dicarboxylate
  • 2-(tert-Butoxycarbonyl)isoindoline-1-carboxylic acid
  • 2-[(2-Methylpropan-2-yl)oxycarbonyl]-1,3-dihydroisoindole-1-carboxylic acid
  • 2H-isoindole-1,2-dicarboxylic acid, 1,3-dihydro-, 2-(1,1-dimethylethyl) ester
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