96546-38-2

Basic information

• Product Name: 3-phenyl-6,7-dihydro-1H-indazol-4(5H)-one
• CAS NO: 96546-38-2
• Molecular Weight: 212.251
• Mol File: 96546-38-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-phenyl-6,7-dihydro-1H-indazol-4(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-phenyl-6,7-dihydro-1H-indazol-4(5H)-one(96546-38-2)
• EPA Substance Registry System: 3-phenyl-6,7-dihydro-1H-indazol-4(5H)-one(96546-38-2)

Safety Data

• Hazardous Substances Data: 96546-38-2(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 102921-12-0 3-<<(4-methylphenyl)sulfonyl>hydrazino>cyclohex-2-en-1-one 
• 504-02-9 1,3-cylohexanedione 
• 69629-50-1 2-benzoyl-1,3-cyclohexanedione 

Downstream Products

• 41555-61-7 1-benzyl-3-phenyl-1,5,6,7-tetrahydro-4H-indazol-4-one 
• 1446335-57-4 2-benzyl-3-phenyl-2,5,6,7-tetrahydro-4H-indazol-4-one 
• 1446335-61-0 1-(4-methoxybenzyl)-3-phenyl-1,5,6,7-tetrahydro-4H-indazol-4-one 
• 1446335-65-4 2-(4-methoxybenzyl)-3-phenyl-2,5,6,7-tetrahydro-4H-indazol-4-one 
• 1446335-69-8 1-(3,4-dimethoxybenzyl)-3-phenyl-1,5,6,7-tetrahydro-4H-indazol-4-one 
• 1446335-73-4 3-phenyl-1-(3,4,5-trimethoxybenzyl)-1,5,6,7-tetrahydro-4H-indazol-4-one 
• 1446336-47-5 6-benzyl-8-phenyl-5,6-dihydro-4H-[1,2]oxazolo[5,4-e]indazole 
• 1446336-51-1 7-benzyl-8-phenyl-5,7-dihydro-4H-[1,2]oxazolo[5,4-e]indazole 
• 1446336-55-5 6-(4-methoxylbenzyl)-8-phenyl-5,6-dihydro-4H-[1,2]oxazolo[5,4-e]indazole 
• 1446336-59-9 7-(4-methoxybenzyl)-8-phenyl-5,7-dihydro-4H-[1,2]oxazolo[5,4-e]indazole 
• 1446336-63-5 6-(3,4-dimethoxylbenzyl)-8-phenyl-5,6-dihydro-4H-[1,2]oxazolo[5,4-e]indazole 
• 1446336-67-9 8-phenyl-6-(3,4,5-trimethoxylbenzyl)-5,6-dihydro-4H-[1,2]oxazolo[5,4-e]indazole 
• 1446335-92-7 1-benzyl-5-[(dimethylamino)methylidene]-3-phenyl-1,5,6,7-tetrahydro-4H-indazol-4-one 
• 1446335-96-1 2-benzyl-5-[(dimethylamino)methylidene]-3-phenyl-2,5,6,7-tetrahydro-4H-indazol-4-one 

Relevant articles and documents

Pd-catalyzed carbonylation for the construction of tertiary and quaternary carbon centers with sp3 carbon partners

The first examples of a Pd-catalyzed carbonylation of aryl boronic acids with sp3 carbon partners are presented. Various boronic acids were shown to react with 1,3-diesters and 1,3-diketones to afford structurally unique carbonyl compounds. By

A VERSATILE SYNTHESIS OF SUBSTITUTED INDAZOLES

A four-step synthetic sequence for substituted indazoles was presented from 2-acylcyclohexane-1,3-diones via either simultaneous or stepwise dehydration and dehydrogenation of 4-substituted 4-hydroxy-4,5,6,7-tetrahydroindazoles as a key step.