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CAS 1469-48-3

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cis-1,2,3,6-Tetrahydrophthalimide

Description:
Cis-1,2,3,6-Tetrahydrophthalimide is a cyclic imide compound characterized by its unique molecular structure, which includes a five-membered ring containing both carbon and nitrogen atoms. This compound is typically a white to off-white solid at room temperature and is known for its relatively low solubility in water, while being more soluble in organic solvents such as ethanol and acetone. It exhibits moderate stability under standard conditions but can undergo hydrolysis in the presence of strong acids or bases. The presence of the imide functional group contributes to its reactivity, allowing it to participate in various chemical reactions, including nucleophilic substitutions. Cis-1,2,3,6-Tetrahydrophthalimide is often utilized in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. Its specific stereochemistry, indicated by the "cis" designation, can influence its biological activity and interaction with other molecules. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.
Formula:C8H9NO2
InChI:InChI=1/C8H9NO2/c10-7-5-3-1-2-4-6(5)8(11)9-7/h1-2,5-6H,3-4H2,(H,9,10,11)/t5-,6+
InChI key:InChIKey=CIFFBTOJCKSRJY-OLQVQODUNA-N
SMILES:O=C1[C@@]2([C@](C(=O)N1)(CC=CC2)[H])[H]
Synonyms:
  • (3aR,7aS)-3a,4,7,7a-tetrahydro-1H-isoindole-1,3(2H)-dione
  • 1H-Isoindole-1,3(2H)-dione, 3a,4,7,7a-tetrahydro-, (3aR,7aS)-rel-
  • 1H-Isoindole-1,3(2H)-dione, 3a,4,7,7a-tetrahydro-, cis-
  • 1H-Isoindole-1,3(2H)-dione, tetrahydro-
  • 1H-Isoindole-1,3(2H)-dione,3a,4,7,7a-tetrahydro-
  • 3,4,5,6-Tetrahydrophthalimide
  • 3a,4,7,7a-tetrahydro-1H-isoindole-1,3(2H)-dione
  • 4,5,6,7-Tetrahydroisoindole-1,3-dione
  • 4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione
  • 4-Cyclohexene-1,2-dicarboximide
  • See more synonyms
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