91375-06-3

Basic information

• Product Name: 2,5-Pyrrolidinedione, 1-[2-(1-cyclohexen-1-yl)ethyl]-
• CAS NO: 91375-06-3
• Molecular Formula: C12H17NO2
• Molecular Weight: 207.272
• Mol File: 91375-06-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,5-Pyrrolidinedione, 1-[2-(1-cyclohexen-1-yl)ethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Pyrrolidinedione, 1-[2-(1-cyclohexen-1-yl)ethyl]-(91375-06-3)
• EPA Substance Registry System: 2,5-Pyrrolidinedione, 1-[2-(1-cyclohexen-1-yl)ethyl]-(91375-06-3)

Safety Data

• Hazardous Substances Data: 91375-06-3(Hazardous Substances Data)

Upstream product

• 108-30-5 succinic acid anhydride 
• 3399-73-3 2-(1-cyclohexenyl)ethylamine 
• 108-94-1 cyclohexanone 
• 6975-71-9 1-cyclohexenylacetonitrile 

Downstream Products

• 91375-16-5 6-Cyclohex-1-enyl-azepane-2,5-dione 
• 91375-17-6 9a-Hydroxy-1,2,3,4b,5,6,8,9,9a,9b-decahydro-6-aza-benzo[3,4]cyclobuta[1,2]cyclohepten-7-one 

Relevant articles and documents

Photochemistry of Succinimides with a Cycloalkenylalkyl Group in the Side Chain. Competitive Norrish Type II and Paterno-Buchi Reactions

Photolysis of N-succinimides (9c-f) (m>/=2) afforded mainly azepinediones (13c-f) with ring enlargement as the Norrish type II cyclization products.In the case of m=1, spiro-azepinedione derivatives (11a, b) were obtained in addition to tricyclic nitrogen heterocycles (10a, b), the Norrish type II products.These spiro-azepinediones are probably formed via imide imide-oxetanes by the intramolecular Paterno-Buchi reaction of these succinimides in competition with the type II processes.Keywords: N-succinimide; Norrish type II reaction; oxetane formation; azepinedione; spiro compound; photochemistry.