74209-51-1

Basic information

• Product Name: Ethanone, 1-(3-pyridinyl)-, O-[(4-methylphenyl)sulfonyl]oxime
• Synonyms: 1-(3-pyridinyl)-ethanone O-[(4-methylphenyl)sulphonyl]-oxime
• CAS NO: 74209-51-1
• Molecular Formula: C14H14N2O3S
• Molecular Weight: 290.343
• Mol File: 74209-51-1.mol
• Article Data: 5

Chemical Properties

• Melting Point: 77-79 °C(Solv: ethanol (64-17-5); water (7732-18-5))
• Boiling Point: 441.9±47.0 °C(Predicted)
• Density: 1.23±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Ethanone, 1-(3-pyridinyl)-, O-[(4-methylphenyl)sulfonyl]oxime(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(3-pyridinyl)-, O-[(4-methylphenyl)sulfonyl]oxime(74209-51-1)
• EPA Substance Registry System: Ethanone, 1-(3-pyridinyl)-, O-[(4-methylphenyl)sulfonyl]oxime(74209-51-1)

Safety Data

• Hazardous Substances Data: 74209-51-1(Hazardous Substances Data)

Upstream product

• 106881-77-0 (E)-1-(pyridin-3-yl)ethanone oxime 
• 98-59-9 p-toluenesulfonyl chloride 
• 350-03-8 methyl-3-pyridylketone 
• 5973-83-1 1-(pyridin-3-yl)ethan-1-one oxime 

Downstream Products

• 93103-29-8 4-(pyridin-3-yl)-1H-imidazole-2(3H)-thione 
• 51746-85-1 3-(1H-imidazol-4-yl)pyridine 
• 1233855-18-9 N-cyclohexyl-N-methyl-4-(pyridin-3-yl)-1H-imidazole-1-carboxamide 
• 1233855-46-3 3-(1-(cyclohexyl(methyl)carbamoyl)-1H-imidazol-4-yl)pyridine 1-oxide 
• 1356960-88-7 C₁₅H₁₁N₃O₂ 
• 1356960-60-5 N-benzyl-N-methyl-4-(pyridin-3-yl)-1H-imidazole-1-carboxamide 
• 51746-82-8 2-amino-1-pyridin-3-yl-ethanone dihydrochloride salt 
• 173838-67-0 4-(3-pyridyl)-1H-imidazol-1-butanamide phthalimide 
• 93103-29-8 4-Pyridin-3-yl-1H-imidazole-2-thiol 
• 51941-15-2 3-(α-aminoacetyl)pyridine 
• 107445-24-9 2,2-diethoxy-2-(3-pyridyl)ethylamine dihydrochloride 
• 254430-68-7 3-(2H-azirin-3-yl)pyridine 

Relevant articles and documents

Synthesis and Antibacterial Activity of Novel 4″-O-desosaminyl clarithromycin derivatives with 11, 12-arylalkyl side chains

A series of novel 4″-O-desosaminyl clarithromycin derivatives with 11, 12-arylalkyl side chains was synthesized by coupling 6-deoxy-desosamine donors (18, 19) with 4″-OH of compounds 5a–c. The activities of the target compounds were tested against a series of macrolide-sensitive and macrolide-resistant pathogens. Some of them showed activities against macrolide sensitive and resistant pathogens, and compounds 21d and 21e displayed significant improvement of activities against resistant pathogens.

Efficient synthesis of 2-imidazol-2-ylacetates

A simple method of synthesizing various 2-imidazol-2-ylacetates is described. Condensation of α-aminoketals with imidates, followed by cyclization in refluxing 4 M-HCl/Dioxane, yielded 2-imidazol-2-ylacetates under one-pot and mild reaction conditions.

Gamma-hydroxy-2-(fluoroalkylaminocarbonyl)-1-piperazinepentanamides and uses thereof

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