1441-99-2

Basic information

• Product Name: Ethanone, 1-[3-(methylthio)phenyl]-
• CAS NO: 1441-99-2
• Molecular Formula: C9H10OS
• Molecular Weight: 166.244
• Mol File: 1441-99-2.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[3-(methylthio)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[3-(methylthio)phenyl]-(1441-99-2)
• EPA Substance Registry System: Ethanone, 1-[3-(methylthio)phenyl]-(1441-99-2)

Safety Data

• Hazardous Substances Data: 1441-99-2(Hazardous Substances Data)

Upstream product

• 99-03-6 1-(3-aminophenyl)ethanone 
• 77-78-1 dimethyl sulfate 
• 33733-73-2 3-bromo-1-(methylthio)benzene 
• 75-36-5 acetyl chloride 
• 3814-19-5 1-(3-mercaptophenyl)ethanone 
• 1783-81-9 3-methylmercaptoaniline 
• 431-03-8 dimethylglyoxal 
• 13532-18-8 methyl 3-(methylthio)propionate 
• 138313-22-1 3-acetylphenyl trifluoromethanesulfonate 
• 5188-07-8 sodium thiomethoxide 
• 14452-30-3 3'-iodoacetophenone 
• 73035-16-2 3-acetylbenzene-1-sulfonyl chloride 
• 74-88-4 methyl iodide 
• 2142-63-4 1-(3-Bromophenyl)ethanone 

Downstream Products

• 117979-30-3 3-methyl-(E)-N-<1-<3-(methylthio)phenyl>ethylidene>-4H-1,2,4-triazol-4-amine 
• 6136-68-1 3-acethylbenzonitrile 
• 89102-48-7 2-bromo-1-(3-mercaptophenyl)ethanone 
• 58114-07-1 m-Methylthio-α-methylbenzylchlorid 
• 117979-37-0 (E,E)-N-<3-(dimethylamino)-1-<3-(methylthio)phenyl>-2-propenylidene>-3-methyl-4H-1,2,4-triazol-4-amine 
• 117979-39-2 3-methyl-6-<3-(methylthio)phenyl>-1,2,4-triazolo<4,3-b>pyridazine 
• 98-86-2 acetophenone 
• 58114-13-9 m-Methylthio-α-methylbenzylalkohol 
• 94001-58-8 1-(3-methylsulfanyl-phenyl)-1-phenyl-ethanol 

Relevant articles and documents

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A green and efficient visible-light induced functionalization of anilines under mild conditions has been reported. Utilizing nontoxic, cost-effective, and water-soluble diacetyl as photosensitizer and acetylating reagent, and water as the solvent, a variety of anilines were converted into the corresponding aryl ketones, iodides, and bromides. With advantages of environmentally friendly conditions, simple operation, broad substrate scope, and functional group tolerance, this reaction represents a valuable method in organic synthesis.

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