19859-79-1

Basic information

• Product Name: Ethanone, 2-(acetyloxy)-1-(2-furanyl)-
• Synonyms: 2-Acetoxy-1-<2>furyl-ethan-1-on;2-furoylmethyl acetate;2-acetoxy-1-furan-2-yl-ethanone
• CAS NO: 19859-79-1
• Molecular Formula: C8H8O4
• Molecular Weight: 168.14700
• Mol File: 19859-79-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-(acetyloxy)-1-(2-furanyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-(acetyloxy)-1-(2-furanyl)-(19859-79-1)
• EPA Substance Registry System: Ethanone, 2-(acetyloxy)-1-(2-furanyl)-(19859-79-1)

Safety Data

• Hazardous Substances Data: 19859-79-1(Hazardous Substances Data)

Upstream product

• 55984-17-3 2-chloroacetylfuran 
• 64-19-7 acetic acid 
• 1192-62-7 1-(2-furyl)-1-ethanone 
• 67-56-1 methanol 
• 62889-08-1 1-(2-furyl)-1-(trimethylsilyloxy)ethylene 
• 15109-94-1 1-(2-furyl)-2-bromoethanone 
• 127-09-3 sodium acetate 
• 177750-22-0 N-acetyl-α-(2-furanyl) ethenamine 
• 127-08-2 potassium acetate 
• 127-19-5 N,N-dimethyl acetamide 

Downstream Products

• 17678-19-2 2-(2-hydroxyacetyl)furan 
• 1245794-45-9 C₁₄H₁₁N₃O₃ 
• 1245794-44-8 1-methyl-2-phenyl-5-(5'-bromo-2'-furyl)imidazole 
• 1245794-39-1 C₁₅H₁₄N₂O₂ 
• 1245794-38-0 C₂₁H₁₆N₂O₂ 
• 1245794-37-9 C₁₆H₁₄N₂O₂ 
• 1245794-36-8 C₁₅H₁₂N₂O₂ 

Relevant articles and documents

Synthesis and properties of 2,5-bis(furan-2-yl)-1H-imidazole

2,5-Bis(furan-2-yl)-1H-imidazole was synthesized by the Weidenhagen reaction of [2-(furan-2-yl)-2-oxoethyl]acetate with furfural. Alkylation of the title compound with methyl iodide in acetone in the presence of potassium hydroxide gave a mixture of isome

Novel and efficient transformation of enamides into α-acyloxy ketones via an acyl intramolecular migration process

Hydrogen peroxide and anhydride mediated transformation of enamides to afford substituted α-acyloxy ketones is described. This transition-metal-free cascade reaction has a broad substrate scope and high efficiency. The acyl intramolecular migration procedure successfully achieved this acyloxylation process under mild conditions and increased the atom efficiency.

Synthesis and properties of 1-methyl-2-phenyl-5-(2-furyl)- and 1-methyl-2-phenyl-5-(2-thienyl)imidazoles

2-Phenyl-5-(2-furyl)- and 2-phenyl-5-(2-thienyl)imidazoles were synthesized by condensation of 2-furoylmethyl and 2-thenoylmethyl acetates with benzaldehyde under the conditions of Weidenhagen reaction. The products were converted to N-methyl derivatives in the KOH-acetone system. The electrophilic substitution reactions of the products (acylation, bromination, nitration, sulfonation, hydroxymethylation) were studied.