219-92-1

Basic information

• Product Name: dibenzocycloheptene
• Synonyms: dibenzocycloheptene
• CAS NO: 219-92-1
• Molecular Weight: 192.26
• Mol File: 219-92-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: dibenzocycloheptene(CAS DataBase Reference)
• NIST Chemistry Reference: dibenzocycloheptene(219-92-1)
• EPA Substance Registry System: dibenzocycloheptene(219-92-1)

Safety Data

• Hazardous Substances Data: 219-92-1(Hazardous Substances Data)

Upstream product

• 118-92-3 anthranilic acid 
• 7443-47-2 5-Cyan-5,7-dihydro-6H-dibenzocyclohepten 
• 3526-27-0 biphenyl-2,2'-diyldi-acetonitrile 
• 1139-82-8 5,7-dihydro-dibenzo[a,c]cyclohepten-6-one 
• 3594-99-8 dibenzocycloheptan-6-ol 
• 5807-64-7 diphenic acid dimethyl ester 
• 863305-32-2 diphenic acid 
• 38274-14-5 2,2'-bis-(bromomethyl)-1,1'-biphenyl 
• 3594-90-9 2,2'-bis(hydroxymethyl)biphenyl 
• 85-01-8 phenanthrene 
• 264-08-4 benzocycloheptatrien 
• 4860-44-0 6,7-dihydro-5H-dibenzo[a,c]cyclohepten-6-ylamine; hydrochloride 

Downstream Products

• 883-20-5 9-methylphenanthrene 
• 837-45-6 phenanthrene-9-carboxylic acid 
• 84-11-7 9,10-phenanthrenequinone 
• 7125-62-4 1,2-benzo-1,3-cycloheptadiene 
• 1075-16-7 6,7,8,9-tetrahydro-5H-benzo[7]annulene 
• 264-08-4 benzocycloheptatrien 
• 1015-80-1 6,7-dihydro-5H-dibenzo[a,c][7]annulene 
• 90-12-0 1-Methylnaphthalene 
• 91-57-6 2-Methylnaphthalene 
• 217-22-1 Dibenzocyclooctatetraene 
• 53137-51-2 6,7-dihydro-5H-dibenzocyclohepten-5-one 
• 832-71-3 3-methylphenathrene 
• 85-01-8 phenanthrene 
• 949-41-7 1a,9b-dihydro-cyclopropa[1]phenanthrene 

Relevant articles and documents

Flow-vacuum pyrolysis of dibenzocycloheptane annelated derivative on zeolites catalysts

The pyrolysis of 5H-6,7-dihydrodibenzo[a,c]cyclohepten-6-ol (5) in FVP conditions, a method of thermal decomposition in advanced vacuum, inert atmosphere on zeolites/acid Al2O3 at variable temperature between 300- 350° C is presented. The reaction products were identified by GC/MS using authentic samples and a reaction mechanism involving cationic species as intermediates was proposed. A comparison with the pyrolysis of the same compound performed in FVP conditions on quartz is presented.