39061-31-9

Basic information

• Product Name: 2-cyclohexyl-1H-benzo[de]isoquinoline-1,3(2H)-dione
• Synonyms: 2-cyclohexyl-1H-benzo[de]isoquinoline-1,3(2H)-dione
• CAS NO: 39061-31-9
• Molecular Formula: C₁₈H₁₇NO₂
• Molecular Weight: 279.33308
• Mol File: 39061-31-9.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-cyclohexyl-1H-benzo[de]isoquinoline-1,3(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-cyclohexyl-1H-benzo[de]isoquinoline-1,3(2H)-dione(39061-31-9)
• EPA Substance Registry System: 2-cyclohexyl-1H-benzo[de]isoquinoline-1,3(2H)-dione(39061-31-9)

Safety Data

• Hazardous Substances Data: 39061-31-9(Hazardous Substances Data)

Upstream product

• 81-84-5 1,8-Naphthalic anhydride 
• 108-91-8 cyclohexylamine 
• 105089-47-2 N-bromo-1,8-naphthalenedicarboximide 
• 110-83-8 cyclohexene 
• 4998-76-9 cyclohexylamine hydrochloride 

Downstream Products

• 41572-86-5 N,N'-bis(cyclohexyl)perylene-3,4,9,10-tetracarboxylic acid diimide 

Relevant articles and documents

Aggregation-induced emission, multiple chromisms and self-organization of N-substituted-1,8-naphthalimides

Most aggregation-induced emission (AIE) luminogens possess propeller-like aromatic stator-rotor structures, such as silole, tetraphenylethylene (TPE) and triphenylamine (TPA), to restrict intra-molecular motions (RIM) and avoid aggregation-caused quenchin

Ionic liquids accelerate access to N-substituted-1,8-naphthalimides

The synthesis of N-substituted-1,8-naphthalimides is accelerated in the presence of the room temperature ionic liquid [BMIM][NO3]. Reaction times are reduced from 18 h in volatile organic compounds (VOCs) (PhCH 3, EtOH and THF) to 20 min in the ionic liquid [BMIM][NO 3]. The reaction yields are typically increased to >85% and the products are isolated by ethanol-mediated precipitation direct from the ionic liquid, requiring no further purification. Crown Copyright

Stereoselectivity of Radical Additions of N-Haloimides to Cyclic Alkenes

The addition of N-haloimides (1-5) to alkenes 9 via imidyl radicals 6-8 introduces a halogen atom and an imidyl moiety to vicinal C-atoms of a carbon chain. With cyclic alkenes, the trans/cis-stereoselectivity depends on the nature of the imidyl unit, on the halogen atom, and on the alkene and varied between 58 : 42 and >95 : 5. Temperature dependend studies showed higher trans/cis-selectivities at elevated temperatures, which may be caused by different conformations of the adduct radicals 10-12, each of them exhibiting a different stereoselectivity.