58303-62-1

Basic information

• Product Name: 2,3-Furandione, 5-(4-chlorophenyl)-
• CAS NO: 58303-62-1
• Molecular Formula: C10H5ClO3
• Molecular Weight: 208.601
• Mol File: 58303-62-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2,3-Furandione, 5-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Furandione, 5-(4-chlorophenyl)-(58303-62-1)
• EPA Substance Registry System: 2,3-Furandione, 5-(4-chlorophenyl)-(58303-62-1)

Safety Data

• Hazardous Substances Data: 58303-62-1(Hazardous Substances Data)

Upstream product

• 38053-20-2 4-(4-chlorophenyl)-2,4-dioxobutanoic acid 
• 103344-71-4 (Z)-4-(4-chlorophenyl)-2-hydroxy-4-oxobut-2-enoic acid 
• 88330-75-0 4-(4-chlorophenyl)-2,4-dioxobutyric acid ethyl ester sodium salt 
• 99-91-2 para-chloroacetophenone 
• 79-37-8 oxalyl dichloride 
• 58518-76-6 ((1-(4-chlorophenyl)vinyl)oxy)trimethylsilane 

Downstream Products

• 130421-41-9 4-(4-Chloro-phenyl)-2,4-dioxo-N-thiazol-2-yl-butyramide 
• 77092-31-0 6-(4-Chloro-phenyl)-2-methyl-4-oxo-4H-[1,3]dioxine-2-carboxylic acid ethyl ester 
• 78344-67-9 ethyl 5-(4-chlorophenyl)-2-diazo-3,5-dioxopentanoate 
• 132680-87-6 C₁₇H₁₂ClNO₅ 
• 113721-96-3 3-(4-Chloro-phenyl)-3-oxo-propionic acid 4-nitro-phenyl ester 
• 132680-88-7 C₁₄H₉ClN₂O₆ 
• 132680-86-5 C₁₇H₁₁ClN₂O₇ 
• 17822-43-4 3-benzoyl-5-(4-chloro-benzoyl)-1⁽²⁾H-pyrazol-4-ol 
• 93795-51-8 6-(4-Chloro-phenyl)-2-dibutylamino-[1,3]oxazin-4-one 
• 121400-66-6 5-[2-(4-Chloro-phenyl)-2-oxo-eth-(E)-ylidene]-3-hydroxy-imidazolidine-2,4-dione 
• 93795-48-3 6-(4-Chloro-phenyl)-2-diallylamino-[1,3]oxazin-4-one 
• 121400-59-7 6-[2-(4-Chloro-phenyl)-2-oxo-eth-(E)-ylidene]-piperazine-2,3,5-trione 2,3-dioxime 
• 107853-64-5 2-[(E)-tert-Butylimino]-5-(4-chloro-phenyl)-furan-3-one 
• 122351-41-1 5-[2-(4-Chloro-phenyl)-2-oxo-eth-(E)-ylidene]-3-phenyl-imidazolidine-2,4-dione 

Relevant articles and documents

Furan-2,3-diones as masked dipoles: synthesis of isotetronic acids and mechanistic considerations

The formal dipolar behaviour of furan-2,3-diones is illustrated by their reaction with ethyl glyoxylate under Lewis basic activation uniquely, giving access to isotetronic derivatives. The Janus-type nature of the activated species, both nucleophilic and

1,3,4,6-Tetracarbonyl compounds. 3. Synthesis, structural features, and antimicrobial activity of 1,6-diaryl-3,4-dihydroxy-2,4-hexadiene-1,6-diones

The Wittig reaction of 5-aryl-2,3-dihydro-2,3-furandiones with aroylmethylenetriphenylphosphoranes is regioselective and leads to the formation of 5-aryl-2-aroylmethylene-2,3-dihydro-3-furanones. In the presence of acid the products react with water, givi

Reactions of 5-aryl-furan-2,3-diones with acylmethylenetriphenylphosphoranes: Synthesis and biological activity of 3(2H)-furanone derivatives

The Wittig reaction of 5-aryl-furan-2,3-diones 1 with acylmethylenetriphenylphosphoranes 2 conducted by heating under reflux in benzene solutions, proceeded regiospecifically to afford 2-acylmethylene-5-aryl-3(2H)-furanones 5 in good yields. When the star