909095-75-6

Basic information

• Product Name: 2-(4-chloro-2-methylsulfanylpyrimidin-5-yl)-1-(2,6-dichlorophenyl)ethanone
• Synonyms: 2-(4-chloro-2-methylsulfanylpyrimidin-5-yl)-1-(2,6-dichlorophenyl)ethanone
• CAS NO: 909095-75-6
• Molecular Weight: 347.652
• Mol File: 909095-75-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(4-chloro-2-methylsulfanylpyrimidin-5-yl)-1-(2,6-dichlorophenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-chloro-2-methylsulfanylpyrimidin-5-yl)-1-(2,6-dichlorophenyl)ethanone(909095-75-6)
• EPA Substance Registry System: 2-(4-chloro-2-methylsulfanylpyrimidin-5-yl)-1-(2,6-dichlorophenyl)ethanone(909095-75-6)

Safety Data

• Hazardous Substances Data: 909095-75-6(Hazardous Substances Data)

Upstream product

• 83-38-5 2,6-dichlorobenzaldehyde 
• 61044-96-0 4-chloro-5-methyl-2-(methylsulfanyl)pyrimidine 
• 909095-74-5 5-bromomethyl-4-chloro-2-(methylthio)pyrimidine 
• 93554-97-3 (+/-)-2-(2,6-dichlorophenyl)-2-(trimethylsiloxy)-acetonitrile 

Downstream Products

• 909095-76-7 1-(2,6-dichloro-phenyl)-2-[4-(N,N'-dimethyl-hydrazino)-2-methylsulfanyl-pyrimidin-5-yl]-ethanone 
• 909095-82-5 4-(2,6-dichlorophenyl)-8-methylsulfinyl-1,2-dihydro-3a,7,9,9b-tetraazacyclopenta[a]naphthalen-3-one 
• 916907-11-4 4-(2,6-dichlorophenyl)-4-hydroxy-8-methylsulfanyl-1,2,4,5-tetrahydro-3a,7,9,9b-tetraazacyclopenta[a]naphthalen-3-one 
• 909095-79-0 4-(2,6-dichlorophenyl)-8-methylsulfanyl-1,2-dihydro-3a,7,9,9b-tetraazacyclopenta[a]naphthalen-3-one 
• 909095-77-8 3-(2,6-dichlorophenyl)-1,2-dimethyl-7-methylsulfanyl-1,2-dihydropyrimido[4,5-c]pyridazine 
• 909095-78-9 1-{5-[2-(2,6-dichlorophenyl)-3-oxoethyl]-2-methylsulfanylpyrimidin-4-yl}pyrazolidin-3-one 

Relevant articles and documents

The development of novel 1,2-dihydro-pyrimido[4,5-c]pyridazine based inhibitors of lymphocyte specific kinase (Lck)

This communication details the synthesis, biological activity, and proposed binding mode of a novel class of tri-cyclic derivatives of 1,2-dihydro-pyrimido[4,5-c]pyridazines 1 and 2. The most potent analogs disclosed showed low nanomolar activity for the