184895-81-6

Basic information

• Product Name: Ethanone, 1-[3-(methylthio)-1,2,4-triazin-5-yl]- (9CI)
• Synonyms: Ethanone, 1-[3-(methylthio)-1,2,4-triazin-5-yl]- (9CI);1-(3-(methylthio)-1,2,4-triazin-5-yl)ethanone
• CAS NO: 184895-81-6
• Molecular Formula: C₆H₇N₃OS
• Molecular Weight: 169.20428
• Product Categories: ACETYLGROUP
• Mol File: 184895-81-6.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ethanone, 1-[3-(methylthio)-1,2,4-triazin-5-yl]- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[3-(methylthio)-1,2,4-triazin-5-yl]- (9CI)(184895-81-6)
• EPA Substance Registry System: Ethanone, 1-[3-(methylthio)-1,2,4-triazin-5-yl]- (9CI)(184895-81-6)

Safety Data

• Hazardous Substances Data: 184895-81-6(Hazardous Substances Data)

Upstream product

• 94243-19-3 5-acetyl-3-methylsulfanyl-1,2,4-triazine oxime 
• 153461-94-0 methyl 3-(methylthio)-1,2,4-triazin-5-yl ketone oxime 

Downstream Products

• 1607820-48-3 4-ethoxy-3-(1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]-triazin-5-yl)benzene-1-sulfonyl chloride 
• 1607820-47-2 3-(2-ethoxyphenyl)-1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]-triazine 
• 310888-52-9 3-methyl-5-(methylsulfanyl)-1-phenyl-1H-pyrazolo[4,3-e][1,2,4]triazine 

Relevant articles and documents

Novel Sulfoneamide Compound and Use Thereof

The present invention relates to a novel sulfonamide compound with tyrosinase and urease inhibitory effects; and uses thereof. The novel sulfonamide compound of the present invention has inhibitory effects on tyrosinase and urease, and thus may be suitabl

Relaxant effects of selected sildenafil analogues in the rat aorta

A new series of sulfonamide derivatives of pyrazolo[4,3-e][1,2,4]triazine with chiral amino group has been synthesized and characterized. The compounds were tested for their relaxant effects in the rat aorta. Evaluation of prepared derivatives demonstrated that compound (8a) is probably a non-selective phosphodiesterase (PDE) inhibitor, as it induced aortic relaxation through endothelium-independent mechanism.

Antiviral activity evaluation of pyrazolo[4,3-e][1,2,4]triazines

The main purpose of this study is to screen synthesized pyrazolo[4,3- e][1,2,4]triazine derivatives for their antiviral activity against a panel of DNA and RNA viruses. Minimum cytotoxic and minimum virus-inhibitory concentrations of these compounds were