25234-74-6

Basic information

• Product Name: 2,5-Hexanedione, 3-phenyl-
• CAS NO: 25234-74-6
• Molecular Formula: C12H14O2
• Molecular Weight: 190.242
• Mol File: 25234-74-6.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2,5-Hexanedione, 3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Hexanedione, 3-phenyl-(25234-74-6)
• EPA Substance Registry System: 2,5-Hexanedione, 3-phenyl-(25234-74-6)

Safety Data

• Hazardous Substances Data: 25234-74-6(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 6430-25-7 acetyl-triphenylgermane 
• 339987-27-8 4-phenyl-5-hexyn-2-one 
• 98-80-6 phenylboronic acid 
• 1134781-54-6 3-acetyl-4-phenyl-hexane-2,5-dione 
• 848302-88-5 C₁₃H₁₄O 
• 38720-22-8 (2-methyl-4-phenyl-1-oxabuta-1,3-diene)tricarbonyliron⁽⁰⁾ 
• 917-54-4 methyllithium 
• 100-52-7 benzaldehyde 
• 546103-01-9 2-acetyl-4-nitro-3-phenyl-valeric acid ethyl ester 
• 705-60-2 1-phenyl-2-nitroprop-1-ene 
• 591-51-5 phenyllithium 
• 66310-18-7 4c-(5-methyl-3-phenyl-[1,4,2]dioxazol-5-yl)-but-3-en-2-one 
• 2039-85-2 3-Chlorostyrene 

Downstream Products

• 19842-57-0 2,5-dimethyl-3-phenylfurane 
• 1312718-25-4 ethyl 2-(2,5-dimethyl-3-phenyl-4-(2-(pyrrolidin-1-ylsulfonyl)benzyl)-1H-pyrrol-1-yl)acetate 
• 1312717-69-3 2-(2,5-dimethyl-3-phenyl-4-(2-(pyrrolidin-1-ylsulfonyl)benzyl)-1H-pyrrol-1-yl)acetic acid 
• 1312718-24-3 ethyl 2-(2,5-dimethyl-3-phenyl-1H-pyrrol-1-yl)acetate 
• 3771-60-6 2,5-dimethyl-3-phenyl-1H-pyrrole 
• 13712-55-5 2,5-Dimethyl-1,3-diphenylpyrrole 

Relevant articles and documents

Enantioface discriminating carbonylations of styrene with cationic palladium(II) catalyst precursors

The enantioface discriminating copolymerization of styrene with carbon monoxide using palladium complexes [(L∧L′)Pd(S)2](X)2 of the C1-symmetric ligands (S,S)-2-[2-(diphenylphosphino)phenyl]-3-phenyl-4-methoxyme

Copper-Catalyzed Three-Component Reactions of α-Ketoaldehyde, 1,3-Dicarbonyl Compound, and Organic Boronic Acid in Water: A Route to 1,4-Diketones

A novel three-component reaction of α-ketoaldehydes, 1,3-dicarbonyl compounds, and organic boronic acids catalyzed by CuO in water has been developed to give a wide range of products containing 1,3/1,4-diketones. The method has some advantages such as the

Novel one-pot vicinal double C-acylation of styrenes and methacrylates by electroreduction

Electroreduction of styrenes or alkyl methacrylates in the presence of aliphatic acid anhydrides or N-acylimidazoles with an undivided cell equipped with zinc electrodes as the anode and the cathode brought about novel one-pot vicinal double C-acylation to afford the corresponding 1,4-diketones in satisfactory yields.