63283-56-7

Basic information

• Product Name: (4'-Methylbiphenyl-4-yl)(phenyl)methanone
• Synonyms: (4'-Methylbiphenyl-4-yl)(phenyl)methanone
• CAS NO: 63283-56-7
• Molecular Formula: C₂₀H₁₆O
• Molecular Weight: 272
• Mol File: 63283-56-7.mol
• Article Data: 25

Chemical Properties

• Melting Point: 129-130℃
• Boiling Point: 429.6±24.0 °C(Predicted)
• Appearance: /
• Density: 1.093±0.06 g/cm3(Predicted)
• CAS DataBase Reference: (4'-Methylbiphenyl-4-yl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4'-Methylbiphenyl-4-yl)(phenyl)methanone(63283-56-7)
• EPA Substance Registry System: (4'-Methylbiphenyl-4-yl)(phenyl)methanone(63283-56-7)

Safety Data

• Hazardous Substances Data: 63283-56-7(Hazardous Substances Data)

Usage

General Description

(4'-Methylbiphenyl-4-yl)(phenyl)methanone, also known as 4-Methyl-4'-biphenylcarbonylphenylmethanone, is a chemical compound with the molecular formula C20H18O. It is a white to off-white crystalline powder that is insoluble in water and soluble in organic solvents. (4'-Methylbiphenyl-4-yl)(phenyl)methanone is used in various applications, including as a building block in the synthesis of pharmaceuticals and other organic compounds. It may also be used as a precursor in the production of specialty chemicals and dyes. Additionally, it has potential uses in the field of material science and can act as a ligand in coordination chemistry. The chemical properties and structure of (4'-Methylbiphenyl-4-yl)(phenyl)methanone make it a versatile and valuable compound for a wide range of industrial and scientific applications.

Upstream product

• 345-83-5 4-fluorobenzophenone 
• 90252-89-4 p-tolylzinc(II) chloride 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 1137-42-4 4-Hydroxybenzophenone 
• 825607-56-5 4-benzoylphenyl dimethylsulfamate 
• 2128-93-0 biphenyl-4-yl-phenyl-methanone 
• 5158-46-3 methylzinc chloride 
• 106-38-7 para-bromotoluene 
• 5720-05-8 4-methylphenylboronic acid 
• 134-85-0 4-chlorobenzophenone 
• 380481-66-3 5,5-dimethyl-2-(4-methylphenyl)-1,3,2-dioxaborinane 
• 31688-74-1 p-PhC(O)C₆H₄NMe₃(+)*I(-) 
• 530-44-9 4-(Dimethylamino)benzophenone 
• 83887-62-1 4-benzoylphenyl methane sulfonate 

Downstream Products

• 1402905-62-7 C₂₆H₂₀ClN 
• 1402905-42-3 C₂₆H₁₉N 
• 1402905-43-4 C₂₆H₁₉N 
• 1402905-44-5 6-(4'-methyl-[1,1'-biphenyl]-4-yl)phenanthridine 
• 140621-36-9 4'-(bromomethyl)-4-biphenylyl phenyl ketone 
• 63242-25-1 diphenyl-4-tolylcarbinol 
• 63242-37-5 4-(Chloro-phenyl-methyl)-4'-methyl-biphenyl 

Relevant articles and documents

Aldehydes and ketones influence reactivity and selectivity in nickel-catalysed Suzuki-Miyaura reactions

The energetically-favorable coordination of aldehydes and ketones-but not esters or amides-to Ni0 during Suzuki-Miyaura reactions can lead either to exquisite selectivity and enhanced reactivity, or to inhibition of the reaction. Aryl halides w

A Highly Efficient Monophosphine Ligand for Parts per Million Levels Pd-Catalyzed Suzuki–Miyaura Coupling of (Hetero)Aryl Chlorides

A new indolylphosphine WK-phos has been synthesized for Pd-catalyzed Suzuki–Miyaura coupling of (hetero)aryl chlorides with (alkyl)arylboronic acids. Comprising this newly developed ligand with palladium(II) acetate, the resulting catalyst system was found to be highly effective in facilitating the reaction even when the catalyst loading reaches parts per million levels (e.g. 10 ppm). These examples represent one of the lowest catalyst loadings reported to date of employing monophosphine (e.g. Ar-PCy2) for Suzuki–Miyaura reactions. The ligand geometry has also been well-characterized by single-crystal X-ray crystallography.

Highly bulky and stable geometry-constrained iminopyridines: Synthesis, structure and application in Pd-catalyzed Suzuki coupling of aryl chlorides

A series of bulky geometry-constrained iminopyridylpalladium chlorides were developed. The steric environment adjacent to the nitrogen atom in the pyridine rings and diimine parts enhanced the thermal stability of the palladium species. Bulkier groups at the imino group stabilized the palladium species and the corresponding palladium chlorides showed high activities in the coupling reaction of aryl chlorides.