60041-88-5

Basic information

• Product Name: 6-fluoro-3-phenyl-1,2,3-benzotriazin-4(3H)-one
• CAS NO: 60041-88-5
• Molecular Formula: C₁₃H₈FN₃O
• Molecular Weight: 241.2205
• Mol File: 60041-88-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 385.8°C at 760 mmHg
• Flash Point: 187.2°C
• Density: 1.36g/cm³
• Vapor Pressure: 3.7E-06mmHg at 25°C
• Refractive Index: 1.664
• CAS DataBase Reference: 6-fluoro-3-phenyl-1,2,3-benzotriazin-4(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-fluoro-3-phenyl-1,2,3-benzotriazin-4(3H)-one(60041-88-5)
• EPA Substance Registry System: 6-fluoro-3-phenyl-1,2,3-benzotriazin-4(3H)-one(60041-88-5)

Safety Data

• Hazardous Substances Data: 60041-88-5(Hazardous Substances Data)

Upstream product

• 60041-89-6 2-amino-5-fluoro-N-phenylbenzamide 
• 62-53-3 aniline 
• 319-24-4 2-amino-5-fluoro-benzoic acid methyl ester 

Downstream Products

• 60041-93-2 5-Fluor-N-phenylanthranilsaeuremorpholid 
• 60041-94-3 6-morpholin-4-yl-3-phenyl-3H-benzo[1,2,3]triazin-4-one 
• 318-31-0 2-fluoro-10H-acridin-9-one 
• 1629-09-0 3-fluoro-N-phenylbenzamide 

Relevant articles and documents

Nickel-Catalyzed Denitrogenative Annulation of 1,2,3-Benzotriazin-4-(3H)-ones with Benzynes for Construction of Phenanthridinone Scaffolds

The synthesis of phenanthridinones via denitrogenative annulation of 1,2,3-benzotriazin-4-(3H)-ones with arynes catalysed by Ni(0)/dppm was successfully developed. A variety of phenanthridinones were prepared in good to excellent yields. Based on this method, nature product, N-methylcrinasidine, was synthesized. (Figure presented.).

Potassium Iodide/tert-Butyl Hydroperoxide-Mediated Oxidative Annulation for the Selective Synthesis of N-Substituted 1,2,3-Benzotriazine-4(3H)-ones Using Nitromethane as the Nitrogen Synthon

A novel and efficient oxidative annulation of 2-aminobenzamides with nitromethane has been developed for the chemoselective synthesis of N-substituted 1,2,3-benzotriazine-4(3H)-ones in moderate to excellent yields under transition metal-free conditions. T