151295-36-2

Basic information

• Product Name: 8-Fluoro-2-methyl-1,6-dioxo-9-[4-(2-trifluoromethyl-benzyl)-piperazin-1-yl]-2,3-dihydro-1H,6H-1λ⁴-thia-3a-aza-phenalene-5-carboxylic acid ethyl ester
• Synonyms: 8-Fluoro-2-methyl-1,6-dioxo-9-[4-(2-trifluoromethyl-benzyl)-piperazin-1-yl]-2,3-dihydro-1H,6H-1λ⁴-thia-3a-aza-phenalene-5-carboxylic acid ethyl ester
• CAS NO: 151295-36-2
• Molecular Weight: 565.589
• Mol File: 151295-36-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 8-Fluoro-2-methyl-1,6-dioxo-9-[4-(2-trifluoromethyl-benzyl)-piperazin-1-yl]-2,3-dihydro-1H,6H-1λ⁴-thia-3a-aza-phenalene-5-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 8-Fluoro-2-methyl-1,6-dioxo-9-[4-(2-trifluoromethyl-benzyl)-piperazin-1-yl]-2,3-dihydro-1H,6H-1λ⁴-thia-3a-aza-phenalene-5-carboxylic acid ethyl ester(151295-36-2)
• EPA Substance Registry System: 8-Fluoro-2-methyl-1,6-dioxo-9-[4-(2-trifluoromethyl-benzyl)-piperazin-1-yl]-2,3-dihydro-1H,6H-1λ⁴-thia-3a-aza-phenalene-5-carboxylic acid ethyl ester(151295-36-2)

Safety Data

• Hazardous Substances Data: 151295-36-2(Hazardous Substances Data)

Upstream product

• 151295-22-6 ethyl 10-chloro-9-fluoro-2-methyl-7-oxo-2,3-dihydro-7H-pyrido<1,2,3-de><1,4>benzothiazine-6-carboxylate 
• 116176-51-3 8-chloro-7-fluoro-2-methyl-3,4-dihydro-2H-1,4-benzothiazine 
• 116176-49-9 S-(2-chloro-3-fluoro-6-nitrophenyl)thiolactic acid 
• 116176-50-2 8-chloro-7-fluoro-2-methyl-3-oxo-3,4-dihydro-2H-1,4-benzothiazine 
• 3847-58-3 2,4-difluoro-3-chloro-nitrobenzene 
• 94022-97-6 1-[2-(trifluoromethyl)-benzyl]piperazine 
• 116176-53-5 ethyl 10-chloro-9-fluoro-2-methyl-7-oxo-2,3-dihydro-7H-pyrido<1,2,3-de><1,4>benzothiazine-6-carboxylate 1-oxide 

Relevant articles and documents

Quinolinecarboxylic Acids. 3. Synthesis and Antibacterial Evaluation of 2-Substituted-7-oxo-2,3-dihydro-7H-pyridobenzothiazine-6-carboxylic Acids Related to Rufloxacin

A series of 2-substituted-7-oxo-2,3-dihydro-7H-pyridobenzothiazine-6-carboxylic acids has been prepared and evaluated for in vitro antibacterial activity.These derivatives were less active than corresponding desmethylated analogues.Among th