271247-34-8

Basic information

• Product Name: 3-(3-trifuoromethylphenyl)-4-(2-methylthiopyrimidin-4-yl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine
• Synonyms: 3-(3-trifuoromethylphenyl)-4-(2-methylthiopyrimidin-4-yl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine
• CAS NO: 271247-34-8
• Molecular Weight: 565.619
• Mol File: 271247-34-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-(3-trifuoromethylphenyl)-4-(2-methylthiopyrimidin-4-yl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3-trifuoromethylphenyl)-4-(2-methylthiopyrimidin-4-yl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine(271247-34-8)
• EPA Substance Registry System: 3-(3-trifuoromethylphenyl)-4-(2-methylthiopyrimidin-4-yl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine(271247-34-8)

Safety Data

• Hazardous Substances Data: 271247-34-8(Hazardous Substances Data)

Upstream product

• 85475-10-1 4-(2-chloroacetyl)piperidine-1-carboxylic acid benzyl ester 
• 200801-88-3 2-(2-Methylsulfanylpyrimidin-4-yl)-1-(3-trifluoromethylphenyl)ethanone 
• 116332-62-8 N-methoxy-N-methyl-3-trifluoromethylbenzamide 
• 14001-63-9 2-methylthio-4-methylpyrimidine 

Downstream Products

• 271247-36-0 (S)-3-(3-trifluoromethylphenyl)-4-[(2-α-methylbenzylamino)pyrimidin-4-yl]-6-(N-carbobenzoxypiperidin-4-yl)pyridazine 
• 271247-18-8 ((S)-1-Phenyl-ethyl)-{4-[6-piperidin-4-yl-3-(3-trifluoromethyl-phenyl)-pyridazin-4-yl]-pyrimidin-2-yl}-amine 
• 853730-35-5 4-[5-{2-[1-(4-fluoro-phenyl)-ethylamino]-pyrimidin-4-yl}-6-(3-trifluoromethyl-phenyl)-pyridazin-3-yl]-piperidine-1-carboxylic acid benzyl ester 
• 853730-34-4 4-[5-(2-methylamino-pyrimidin-4-yl)-6-(3-trifluoromethyl-phenyl)-pyridazin-3-yl]-piperidine-1-carboxylic acid benzyl ester 

Relevant articles and documents

Design and synthesis of potent pyridazine inhibitors of p38 MAP kinase

Novel potent trisubstituted pyridazine inhibitors of p38 MAP (mitogen activated protein) kinase are described that have activity in both cell-based assays of cytokine release and animal models of rheumatoid arthritis. They demonstrated potent inhibition o