5931-91-9

Basic information

• Product Name: 2-OXO-1,3-CYCLOHEXANEDIPROPIONITRILE
• Synonyms: 2-OXO-1,3-CYCLOHEXANEDIPROPIONITRILE;3-[3-(2-cyanoethyl)-2-oxocyclohexyl]propanenitrile
• CAS NO: 5931-91-9
• Molecular Formula: C₁₂H₁₆N₂O
• Molecular Weight: 204.27
• Mol File: 5931-91-9.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-OXO-1,3-CYCLOHEXANEDIPROPIONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-OXO-1,3-CYCLOHEXANEDIPROPIONITRILE(5931-91-9)
• EPA Substance Registry System: 2-OXO-1,3-CYCLOHEXANEDIPROPIONITRILE(5931-91-9)

Safety Data

• Hazardous Substances Data: 5931-91-9(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 107-13-1 acrylonitrile 
• 1125-99-1 1-(1-Cyclohexen-1-yl)pyrrolidine 
• 4594-78-9 cyclohexanone-2-propionitrile 

Downstream Products

• 75637-88-6 3-[3-(2-carboxyethyl)-2-oxocyclohexyl]propanoic acid 

Relevant articles and documents

Dehydrogenation and Isomerization of Butane over Cr Catalysts Supported on H-SSZ-35 Type Zeolites

The dehydrogenation and isomerization of butane to isobutene over Cr catalysts supported on zeolites were investigated. Although a zeolite support, especially with a low Si/Al2 ratio, favors the cracking of butane over its dehydrogenation and isomerization, due to strong solid acidity, the loading of Cr on a zeolite support enhances the dehydrogenation and isomerization of butane. H-SSZ-35 type zeolite, which has a one-dimensional cage-type channel structure, was hydrothermally synthesized using cis,cis,cis-N-methylhexahydrojulolidinium hydroxide as a structure-directing agent (SDA). We found that Cr/H-SSZ-35 (Si/Al2 = 500) showed moderate butane conversion and isobutene selectivity. As a result, the yield of isobutene (conversion of butane x selectivity of isobutene) was the highest among the catalysts used in this study. Its activity at 500 °C remained unchanged for 6 h. Our evidence suggests that butane was dehydrogenated over the zeolite support or Cr2O3 particles, and a proportion of the dehydrogenated products were isomerized to isobutene over the zeolite support.