1192-93-4

Basic information

• Product Name: cyclohepta-2,6-dienone
• Synonyms: cyclohepta-2,6-dienone
• CAS NO: 1192-93-4
• Molecular Weight: 108.14
• Mol File: 1192-93-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: cyclohepta-2,6-dienone(CAS DataBase Reference)
• NIST Chemistry Reference: cyclohepta-2,6-dienone(1192-93-4)
• EPA Substance Registry System: cyclohepta-2,6-dienone(1192-93-4)

Safety Data

• Hazardous Substances Data: 1192-93-4(Hazardous Substances Data)

Upstream product

• 291-64-5 cycloheptane 
• 259173-86-9 2,7-diiodocycloheptanone 

Downstream Products

• 532-24-1 tropinone 
• 29259-80-1 8'-phenyl-spiro[[1,3]dioxolane-2,3'-(8-phospha-bicyclo[3.2.1]octane)] 8'-oxide 
• 29259-76-5 8ξ-oxo-8ξ-phenyl-8λ⁵-phospha-bicyclo[3.2.1]octan-3-one 
• 29259-75-4 8ξ-benzyl-3-oxo-8ξ-phenyl-8-phospha-bicyclo[3.2.1]octanium; chloride 
• 29207-41-8 8,8-dibenzyl-3-oxo-8-phospha-bicyclo[3.2.1]octanium; chloride 
• 29259-86-7 8ξ-benzyl-8ξ-methyl-3-oxo-8-phospha-bicyclo[3.2.1]octanium; iodide 
• 29259-74-3 8ξ-methyl-3-oxo-8ξ-phenyl-8-phospha-bicyclo[3.2.1]octanium; iodide 
• 29259-85-6 8ξ-benzyl-8ξ-oxo-8λ⁵-phospha-bicyclo[3.2.1]octan-3-one 
• 42811-96-1 3-phenyl-3a,5,6,7,8,8a-hexahydro-cyclohepta[d]isoxazol-4-one 
• 55652-69-2 3-(2,4,6-trimethyl-phenyl)-3a,5,6,7,8,8a-hexahydro-cyclohepta[d]isoxazol-4-one 
• 55609-49-9 3-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro-cyclohepta[d]isoxazol-4-one 
• 55609-48-8 3-phenyl-5,6,7,8-tetrahydro-cyclohepta[d]isoxazol-4-one 
• 95054-33-4 8-Methyl-3-phenyl-8-thionia-bicyclo[3.2.1]oct-2-ene; iodide 
• 106591-73-5 Toluene-4-sulfonic acid (1S,3S,5R)-(8-thia-bicyclo[3.2.1]oct-3-yl) ester 

Relevant articles and documents

Effective oxidation of benzylic and alkane C-H bonds catalyzed by sodium o-iodobenzenesulfonate with Oxone as a terminal oxidant under phase-transfer conditions

Catalytic oxidation of benzylic C-H bonds could be efficiently realized using IBS as a catalyst which was generated in situ from the oxidation of sodium 2-iodobenzenesulfonate (1b) by Oxone in the presence of a phase-transfer catalyst, tetra-n-butylammonium hydrogen sulfate, in anhydrous acetonitrile at 60 °C. Various alkylbenzenes, including toluenes and ethylbenzenes, several oxygen-containing functionalities substituted alkylbenzenes, and a cyclic benzyl ether could be efficiently oxidized. And, the same reagent system of cat. 1b/Oxone/cat. n-Bu4NHSO4 could be applied to the effective oxidation of alkanes as well.