1225057-54-4

Basic information

• Product Name: 6-methyl-2-phenyl-2H-indazole
• Synonyms: 6-methyl-2-phenyl-2H-indazole
• CAS NO: 1225057-54-4
• Molecular Weight: 208.263
• Mol File: 1225057-54-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 6-methyl-2-phenyl-2H-indazole(CAS DataBase Reference)
• NIST Chemistry Reference: 6-methyl-2-phenyl-2H-indazole(1225057-54-4)
• EPA Substance Registry System: 6-methyl-2-phenyl-2H-indazole(1225057-54-4)

Safety Data

• Hazardous Substances Data: 1225057-54-4(Hazardous Substances Data)

Upstream product

• 95-78-3 2,5-Dimethylaniline 
• 586-96-9 Nitrosobenzene 
• 824-54-4 2-bromo-4-methylbenzaldehyde 
• 62-53-3 aniline 
• 6415-68-5 N-nitroso-N-phenylglycine 
• 103-01-5 N-Phenylglycine 
• 508191-77-3 3-phenylsydnone 
• 262373-15-9 4-methyl-2-(trimethylsilyl)phenyl trifluoromethanesulfonate 

Relevant articles and documents

Oxidative cross-dehydrogenative coupling (CDC)viaC(sp2)-H bond functionalization:tert-butyl peroxybenzoate (TBPB)-promoted regioselective direct C-3 acylation/benzoylation of 2H-indazoles with aldehydes/benzyl alcohols/styrenes

An efficient, cost-effective, transition-metal-free, oxidative C(sp2)-H/C(sp2)-H cross-dehydrogenative couplingviaa C(sp2)-H bond functionalization protocol for the regioselective direct C-3 acylation/benzoylation of subst

Synthesis method of 2H-indazole and derivatives thereof

The invention discloses a synthetic reaction of 2H-indazole and derivatives thereof under a metal-free condition. The new strategy has the advantages of no metal participation, wide substrate range and good functional group compatibility, and an efficient

Direct Acyl Radical Addition to 2 H-Indazoles Using Ag-Catalyzed Decarboxylative Cross-Coupling of α-Keto Acids

A direct acyl radical addition to 2H-indazoles has been achieved for the first time, where the less-aromatic quinonoid 2H-indazoles readily accepted radical species to the C-3 position. Motivated by the lack of direct acylation strategy for 2H-indazoles, the current method utilizes the radical acceptability of 2H-indazoles, discovering an ambient temperature reaction to provide facile access to a diverse array of 3-acyl-2H-indazoles with three points of structural diversification in 25%-83% yields.