70264-96-9

Basic information

• Product Name: N-methylcyclohexane-1,1-dicarboximide
• Synonyms: N-methylcyclohexane-1,1-dicarboximide
• CAS NO: 70264-96-9
• Molecular Weight: 167.208
• Mol File: 70264-96-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-methylcyclohexane-1,1-dicarboximide(CAS DataBase Reference)
• NIST Chemistry Reference: N-methylcyclohexane-1,1-dicarboximide(70264-96-9)
• EPA Substance Registry System: N-methylcyclohexane-1,1-dicarboximide(70264-96-9)

Safety Data

• Hazardous Substances Data: 70264-96-9(Hazardous Substances Data)

Upstream product

• 636-82-8 cyclohexene-1-carboxylic acid 
• 64090-28-4 2-methylhexahydro-1H-isoindole-1,3(2H)-dione 

Downstream Products

• 71098-99-2 N,N'-dimethylcyclohexane-1,1-dicarboxamide 
• 4630-82-4 methyl cyclohexylcarboxylate 
• 6642-30-4 methyl N-methylcarbamate 
• 71099-00-8 2-methoxy-3-methyl-1-oxa-3-azaspiro<4,5>decan-4-one 

Relevant articles and documents

Photochemistry of Aliphatic Imides. Synthesis of Azetidine-2,4-diones via Photochemical Isomerization of Succinimides and N-Formyl-N-methyl α, β -Unsaturated Amides

Photochemical reactions of alkyl-substituted succinimides and N-formyl-N-methyl α, β -unsaturated amides were studied.Photolysis of succinimide 1 gave azetidine-2,4-dione 2 together with a small amount of 3.The photoinduced ring-contraction reaction is explained in terms of a two-photon mechanism.Similarly, several other succinimide derivates photochemically gave the corresponding azetidine-2,4-diones.In addition, the photochemical cyclization of 3 to 2 was extended to the synthesis of azetidine-2,4-diones from N-formyl-N-methyl α, β -unsaturated amides.