198141-12-7

Basic information

• Product Name: 9H-Pyrido[3,2-b]indol-9-one, 5,6,7,8-tetrahydro-
• CAS NO: 198141-12-7
• Molecular Formula: C11H10N2O
• Molecular Weight: 186.213
• Mol File: 198141-12-7.mol
• Article Data: 4

Chemical Properties

• Melting Point: 265℃
• CAS DataBase Reference: 9H-Pyrido[3,2-b]indol-9-one, 5,6,7,8-tetrahydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 9H-Pyrido[3,2-b]indol-9-one, 5,6,7,8-tetrahydro-(198141-12-7)
• EPA Substance Registry System: 9H-Pyrido[3,2-b]indol-9-one, 5,6,7,8-tetrahydro-(198141-12-7)

Safety Data

• Hazardous Substances Data: 198141-12-7(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 581808-41-5 3-(2-chloro-pyridin-3-ylamino)-2-iodo-cyclohex-2-enone 
• 504-02-9 1,3-cylohexanedione 
• 6298-19-7 2-chloro-3-aminopyridine 
• 5470-18-8 2-Chloro-3-nitropyridine 
• 156666-06-7 2-(tri-n-butylstannyl)-2-cyclohexen-1-one 
• 198141-10-5 3-[(2-chloro-3-pyridinyl)amino]cyclohex-2-en-1-one 

Relevant articles and documents

Rapid and efficient microwave-assisted synthesis of 4-, 5-, 6- and 7-azaindoles

Under microwave irradiation conditions, the imines/enamines formed between aminopyridines and ketones are converted in moderate to good yields to the corresponding 4-, 5-, 6- or 7-azaindoles via the Hegedus-Mori-Heck reaction (intramolecular Heck reaction

Palladium-catalyzed synthesis of 1,2-dihydro-4(3H)-carbazolones. Formal total synthesis of murrayaquinone A

Two sequential palladium-catalyzed reactions are the key steps in a novel synthetic route to 1,2-dihydro-4(3H)-carbazolones. The steps are an intermolecular Stille cross-coupling followed by a reductive N-heteroannulation. A formal total synthesis of murrayaquinone A, employing this sequence, is reported.