443672-17-1

Basic information

• Product Name: 3-(4-fluorophenyl)-2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide
• Synonyms: 3-(4-fluorophenyl)-2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide
• CAS NO: 443672-17-1
• Molecular Weight: 276.291
• Mol File: 443672-17-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-(4-fluorophenyl)-2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-fluorophenyl)-2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide(443672-17-1)
• EPA Substance Registry System: 3-(4-fluorophenyl)-2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide(443672-17-1)

Safety Data

• Hazardous Substances Data: 443672-17-1(Hazardous Substances Data)

Upstream product

• 402-42-6 4-fluoro-1-trichloromethylbenzene 
• 3306-62-5 2-AMINOBENZENESULFONAMIDE 
• 405-50-5 p-Fluorophenylacetic acid 
• 459-56-3 4-fluorobenzylic alcohol 

Relevant articles and documents

Ruthenium-catalysed oxidative synthesis of heterocycles from alcohols

Ruthenium-catalysed hydrogen transfer has been successfully used for the conversion of alcohols into either 2,3-dihydroquinazolines or quinazolines. The choice of reaction conditions allows for the selective formation of either heterocycle and the methodology can also be applied to the sulfonamide analogue.

Transition metal-catalyzed C–H functionalization of arylacetic acids for the synthesis of benzothiadiazine 1,1-dioxides

Copper-catalyzed practical route for the synthesis of benzothiadiazine 1,1-dioxides has been developed. The method involves C–H functionalization of arylacetic acids to form aromatic aldehydes and their subsequent condensation with 2-aminobenzenesulfonami