138040-05-8

Basic information

• Product Name: 2-Cyclohexen-1-one, 3-hydroxy-2-(2-nitrophenyl)-
• CAS NO: 138040-05-8
• Molecular Formula: C12H11NO4
• Molecular Weight: 233.224
• Mol File: 138040-05-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexen-1-one, 3-hydroxy-2-(2-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexen-1-one, 3-hydroxy-2-(2-nitrophenyl)-(138040-05-8)
• EPA Substance Registry System: 2-Cyclohexen-1-one, 3-hydroxy-2-(2-nitrophenyl)-(138040-05-8)

Safety Data

• Hazardous Substances Data: 138040-05-8(Hazardous Substances Data)

Upstream product

• 609-73-4 o-nitroiodobenzene 
• 30182-67-3 1,3-Cyclohexanedione 
• 504-02-9 1,3-cylohexanedione 
• 1493-27-2 ortho-nitrofluorobenzene 

Downstream Products

• 15128-52-6 1,2,3,9-tetrahydro-4H-carbazol-4-one 
• 138040-33-2 (3aS,7aR)-3a-(2-Nitro-phenyl)-1-((R)-1-phenyl-ethyl)-octahydro-indol-4-one 
• 138040-34-3 (3aS,7aS)-3a-(2-Nitro-phenyl)-1-((R)-1-phenyl-ethyl)-octahydro-indol-4-one 
• 138040-15-0 (3aR,7aR)-3a-(2-Nitro-phenyl)-1-((R)-1-phenyl-ethyl)-octahydro-indol-4-one 
• 138040-14-9 (3aR,7aS)-3a-(2-Nitro-phenyl)-1-((R)-1-phenyl-ethyl)-octahydro-indol-4-one 
• 138040-35-4 7-(2-Nitro-phenyl)-oxonane-2,6-dione 

Relevant articles and documents

An easy access to carbazolones and 2,3-disubstituted indoles

Synthesis of carbazol-4-ones, 3,4-dihydrocyclopental-indol-1-one, and indole derivatives by a Fe/AcOH-mediated intramolecular reductive N-heteroannulation of 3-hydroxy-2-(2-nitrophenyl)enones is demonstrated. The same protocol has been extended to access indolocarbazolone and indoloquinolone derivatives. Synthesis ofderivatives by a Fe/AcOH-mediated intramolecular reductive N-heteroannulation strategy is demonstrated. The starting materials were easily accessed from C-arylation of 1,3-diketones by o-nitroiodobenzenes. Copyright

3a-(o-nitrophenyl)octahydroindol-4-ones: Synthesis and spectroscopic analysis

A short entry to 3a-(o-nitrophenyl)octahydroindol-4-ones employing ozonolysis and double reductive amination of 2-allyl-2-(o-nitrophenyl)-1,3-cyclohexanedione (9) is described. The symmetric dione 9 is synthesized in a 50% overall yield from 1,3-cyclohexa