118617-04-2

Basic information

• Product Name: 2,3-endo-4,5-exo-3a-(4-cyanobutyl)-3,3a,4,5-tetrahydro-2H-isoxazolo<2,3-b>isoxazole-2,3:4,5-bis(N-phenyldicarboximide)
• CAS NO: 118617-04-2
• Molecular Weight: 486.484
• Mol File: 118617-04-2.mol

Chemical Properties

• CAS DataBase Reference: 2,3-endo-4,5-exo-3a-(4-cyanobutyl)-3,3a,4,5-tetrahydro-2H-isoxazolo<2,3-b>isoxazole-2,3:4,5-bis(N-phenyldicarboximide)(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-endo-4,5-exo-3a-(4-cyanobutyl)-3,3a,4,5-tetrahydro-2H-isoxazolo<2,3-b>isoxazole-2,3:4,5-bis(N-phenyldicarboximide)(118617-04-2)
• EPA Substance Registry System: 2,3-endo-4,5-exo-3a-(4-cyanobutyl)-3,3a,4,5-tetrahydro-2H-isoxazolo<2,3-b>isoxazole-2,3:4,5-bis(N-phenyldicarboximide)(118617-04-2)

Safety Data

• Hazardous Substances Data: 118617-04-2(Hazardous Substances Data)

Upstream product

• 941-69-5 N-phenyl-maleimide 
• 2209-36-1 4,5,6,7-tetrahydro-2,1,3-benzoxadiazol-N-oxide 

Relevant articles and documents

TANDEM 1,3-DIPOLARARYCYCLOADDITIONS OF CYCLOHEXANE FURAZAN-N-OXIDE WITH N-ARYLMAEIMIDES : NOVEL ENTRY TO SUBSTITUED TETRAHYDRO-2H-ISOXALO-(2,3-b) ISOXAZLES (ISOXAZOLIZIDINES).

The reaction of cyclohexane furazan-N-oxide with substituted N-phenylmaleimides involves succesive 1,3-dipolar cycloadditions leading to isoxazolizidines.

Bridgehead-substituted Isoxazolizidines from the Reaction of Cyclohexane and Other Furazan N-oxides with N-substituted Maleimides. Azolium 1,3-Dipoles.

The reaction of cyclohexane furazan N-oxide with N-substituted maleimides involves successive 1,3-dipolar cycloadditions and gives substituted tetrahydroisoxazoloisoxazoles (isoxazolizidines) containing a pentanonitrile chain at the bridgehead.An x-ray crystal structure is reported for compound 9c, 2,3-endo-4,5-exo-3a-(4-cyanobutyl)-3,3a,4,5-tetrahydro-2H-isoxazoloisozazole-2,3:4,5-bis-.With 4,5-dimethyl- and -diphenyl-furazan N-oxides a similar reaction occurred with loss of a nitrile molecule.