1260400-18-7

Basic information

• Product Name: ethyl 4-(bromoacetyl)-1-(4-chlorophenyl)-5-methyl-1H-pyrazole-3-carboxylate
• Synonyms: ethyl 4-(bromoacetyl)-1-(4-chlorophenyl)-5-methyl-1H-pyrazole-3-carboxylate
• CAS NO: 1260400-18-7
• Molecular Weight: 385.645
• Mol File: 1260400-18-7.mol

Chemical Properties

• CAS DataBase Reference: ethyl 4-(bromoacetyl)-1-(4-chlorophenyl)-5-methyl-1H-pyrazole-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 4-(bromoacetyl)-1-(4-chlorophenyl)-5-methyl-1H-pyrazole-3-carboxylate(1260400-18-7)
• EPA Substance Registry System: ethyl 4-(bromoacetyl)-1-(4-chlorophenyl)-5-methyl-1H-pyrazole-3-carboxylate(1260400-18-7)

Safety Data

• Hazardous Substances Data: 1260400-18-7(Hazardous Substances Data)

Upstream product

• 63514-82-9 ethyl 4-acetyl-1-(4-chlorophenyl)-5-methyl-1H-pyrazole-3-carboxylate 

Downstream Products

• 1260400-36-9 ethyl 4-[2-(1,3-benzothiazol-2-ylsulfanyl)-1-oxoethyl]-1-(4-chlorophenyl)-5-methyl-1H-pyrazole-3-carboxylate 
• 1260400-60-9 ethyl 5-methyl-1-(4-chlorophenyl)-4-{2-[1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanyl]-1-oxoethyl}-1H-pyrazole-3-carboxylate 
• 1260400-44-9 ethyl 1-(4-chlorophenyl)-5-methyl-4-[1-oxo-2-(5-phenyl-1,3,4-oxadiazol-2-ylsulfanyl)ethyl]-1H-pyrazole-3-carboxylate 
• 1260400-53-0 ethyl 1-(4-chlorophenyl)-4-[2-(4,5-diphenyl-4H-1,2,4-triazol-3-ylsulfanyl)-1-oxoethyl]-5-methyl-1H-pyrazole-3-carboxylate 
• 1260400-27-8 ethyl 1-(4-chlorophenyl)-5-methyl-4-(2-phenylsulfanyl-1-oxoethyl)-1H-pyrazole-3-carboxylate 
• 1260400-33-6 ethyl 1-(4-chlorophenyl)-4-[2-(4,6-dimethylpyrimidin-2-ylsulfanyl)-1-oxoethyl]-5-methyl-1H-pyrazole-3-carboxylate 

Relevant articles and documents

Synthesis and Anticancer Activity of 2-Aryl-3-methylbenzofuro[3,2-b]pyrazolo[4,3-e]azepine-4,11(2H,10H)-dione and 2-Aryl-3,7,9-trimethylpyrido[3',2':4,5]thieno[3,2-b]pyrazolo[4,3-e]azepine-4,11(2H,10H)-diones

Abstract: The reactions of ethyl 1-aryl-4-(2-bromoacetyl)-5-methyl-1H-pyrazolocarboxylates with ortho-hydroxybenzonitrile and 4,6-dimethyl-2-thioxo-1,2-dihydropyridine-3-carbonitrile gave previously unknown 2-aryl-3-methylbenzofuro[3,2-b]pyrazolo[4,3-e]az

Synthesis of 2-Aryl-4-(R-sulfanylmethyl)-3-methyl-6,7-dihydro-2H- pyrazolo[3,4-d]pyridazin-7-ones

Bromination of ethyl 1-aryl-4-acetyl-5-methyl-1H-pyrazole-3-carboxylates gave ethyl 1-aryl-4-(bromoacetyl)-5-methyl-1H-pyrazol-3-carboxylates which were used to alkylate benzenethiol and heterocyclic thiones at the sulfur atom. Reactions of the resulting