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CAS 140715-57-7

:

2-(6-bromohexyl)-5-nitroisoindoline-1,3-dione

Description:
2-(6-bromohexyl)-5-nitroisoindoline-1,3-dione, with the CAS number 140715-57-7, is a synthetic organic compound characterized by its isoindoline structure, which features a dione functional group. This compound contains a nitro group and a bromoalkyl substituent, contributing to its unique chemical properties. The presence of the bromohexyl group suggests potential for reactivity, particularly in nucleophilic substitution reactions, while the nitro group can influence the compound's electronic properties and reactivity. The isoindoline core is known for its stability and can participate in various chemical reactions, making this compound of interest in medicinal chemistry and materials science. Its solubility, melting point, and other physical properties would depend on the specific conditions and solvents used. Overall, this compound's structural features suggest potential applications in drug development or as a building block in organic synthesis. However, detailed studies would be necessary to fully understand its reactivity and potential uses.
Formula:C14H15BrN2O4
InChI:InChI=1/C14H15BrN2O4/c15-7-3-1-2-4-8-16-13(18)11-6-5-10(17(20)21)9-12(11)14(16)19/h5-6,9H,1-4,7-8H2
SMILES:C(CCCN1C(=O)c2ccc(cc2C1=O)N(=O)=O)CCBr
Synonyms:
  • 2-(6-bromohexyl)-5-nitro-1H-isoindole-1,3(2H)-dione
  • 2-(6-BROMOHEXYL)-5-NITROISOINDOLINE-1,3-DIONE
  • 1H-Isoindole-1,3(2H)-dione, 2-(6-bromohexyl)-5-nitro-
  • 2-(6-Bromohex-1-yl)-5-nitro-1H-isoindole-1,3(2H)-dione, 2-(6-Bromohex-1-yl)-5-nitroisoindolin-1,3-dione, 2-(6-Bromohex-1-yl)-1,3-dioxo-5-nitroisoindoline
  • N-(6-BROMOHEXYL)-4-NITROPHTHALIMIDE
  • N-(6-Bromohex-1-yl)-4-nitrophthalimide
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