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CAS 1541-26-0

:

2-(2-Cyclohexen-1-yl)-1H-isoindole-1,3(2H)-dione

Description:
2-(2-Cyclohexen-1-yl)-1H-isoindole-1,3(2H)-dione, with the CAS number 1541-26-0, is an organic compound characterized by its unique bicyclic structure, which includes an isoindole moiety and a cyclohexene substituent. This compound typically exhibits a solid state at room temperature and is known for its potential applications in organic synthesis and medicinal chemistry. The presence of the isoindole structure contributes to its reactivity, particularly in electrophilic aromatic substitution reactions. Additionally, the cyclohexene ring can participate in various chemical transformations, making it a versatile intermediate in synthetic pathways. The compound may also display interesting biological activities, although specific studies would be required to elucidate its pharmacological properties. Its solubility characteristics can vary depending on the solvent, and it may be sensitive to light or air, necessitating careful handling and storage. Overall, 2-(2-Cyclohexen-1-yl)-1H-isoindole-1,3(2H)-dione represents a valuable compound in the field of organic chemistry.
Formula:C14H13NO2
InChI:InChI=1S/C14H13NO2/c16-13-11-8-4-5-9-12(11)14(17)15(13)10-6-2-1-3-7-10/h2,4-6,8-10H,1,3,7H2
InChI key:InChIKey=HMTXWVRLPMCEGE-UHFFFAOYSA-N
SMILES:O=C1N(C(=O)C=2C1=CC=CC2)C3CCCC=C3
Synonyms:
  • Phthalimide, N-2-cyclohexen-1-yl-
  • 2-Cyclohex-2-en-1-ylisoindole-1,3-dione
  • 2-(2-Cyclohexen-1-yl)-1H-isoindole-1,3(2H)-dione
  • 1H-Isoindole-1,3(2H)-dione, 2-(2-cyclohexen-1-yl)-
  • 2-(Cyclohex-2-en-1-yl)-2,3-dihydro-1H-isoindole-1,3-dione
  • 2-(cyclohex-2-enyl)isoindoline-1,3-dione
  • 2-(CYCLOHEX-2-EN-1-YL)ISOINDOLINE-1,3-DIONE
  • 2-cyclohex-2-enyl-isoindole-1,3-dione
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