54945-17-4

Basic information

• Product Name: Ethanedione, (4-chlorophenyl)(4-methoxyphenyl)-
• CAS NO: 54945-17-4
• Molecular Formula: C15H11ClO3
• Molecular Weight: 274.704
• Mol File: 54945-17-4.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Ethanedione, (4-chlorophenyl)(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanedione, (4-chlorophenyl)(4-methoxyphenyl)-(54945-17-4)
• EPA Substance Registry System: Ethanedione, (4-chlorophenyl)(4-methoxyphenyl)-(54945-17-4)

Safety Data

• Hazardous Substances Data: 54945-17-4(Hazardous Substances Data)

Upstream product

• 97723-29-0 4-chloro-4'-methoxy-benzoin 
• 54551-72-3 2-(4-chlorophenyl)-2-hydroxy-1-(4-methoxyphenyl)ethan-1-one 
• 1878-66-6 4-chlorophenylacetic Acid 
• 100-66-3 methoxybenzene 
• 64594-43-0 4-chloro-N-(2.6-dimethylphenyl)-benzamide 
• 104-88-1 4-chlorobenzaldehyde 
• 4231-69-0 1-(4-methoxybenzoyl)-1H-1,2,3-benzotriazole 
• 123-11-5 4-methoxy-benzaldehyde 
• 4231-70-3 p-chlorobenzoyl-1H-1,2,3-benzotriazole 
• 5043-91-4 4-chloro-4'-methoxy-stilbene 
• 39672-21-4 1-(4-methoxyphenyl)-2-(4-chlorophenyl)acetylene 
• 6552-68-7 4-chloro-4'-methoxy-chalcone 
• 37613-10-8 4-chloro-N-phenyl-benzimidoyl chloride 
• 13628-99-4 α-bromo-4-chloro-4'-methoxy-deoxybenzoin 

Downstream Products

• 1417560-54-3 2-(4-chlorophenyl)-3-(4-methoxyphenyl)pyrazine 

Relevant articles and documents

1-butyl-3-methylimidazol-2-ylidene as an efficient catalyst for cross-coupling between aromatic aldehydes and N-aroylbenzotriazoles

Cross-coupling of aromatic aldehydes with N-aroylbenzotriazoles in [Bmim]Br in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) provided an efficient procedure for the synthesis of 1,2-diarylethane-1,2-diones.

Ruthenium/dendrimer complex immobilized on silica-functionalized magnetite nanoparticles catalyzed oxidation of stilbenes to benzil derivatives at room temperature

A new ruthenium/dendrimer complex stabilized on the surface of silica-functionalized nano-magnetite was fabricated and well characterized. The nano-catalyst showed good activity in the synthesis of benzil derivatives via the oxidation of stilbenes with high turnover frequency (TOF) at room temperature. Moreover, the catalyst could also be reused up to fifteen times without any loss of its activity.

Selective oxygenation of alkynes: A direct approach to diketones and vinyl acetate

Arylalkynes can be converted into α-diketones with the use of a copper catalyst, and also be transformed into vinyl acetates under metal-free conditions, both in the presence of PhI(OAc)2 as an oxidant at room temperature. A series of substituted α-diketones were prepared in moderate to good yields. A variety of vinyl halides could be regio- and stereo-selectively synthesized under mild conditions, and I, Br and Cl could be all easily embedded into the alkynes. This journal is