64357-69-3

Basic information

• Product Name: (4-cyclohexylphenyl)(phenyl)methanone
• CAS NO: 64357-69-3
• Molecular Formula: C₁₉H₂₀O
• Molecular Weight: 264.3615
• Mol File: 64357-69-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 405.2°C at 760 mmHg
• Flash Point: 176°C
• Density: 1.062g/cm³
• Vapor Pressure: 8.95E-07mmHg at 25°C
• Refractive Index: 1.572
• CAS DataBase Reference: (4-cyclohexylphenyl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4-cyclohexylphenyl)(phenyl)methanone(64357-69-3)
• EPA Substance Registry System: (4-cyclohexylphenyl)(phenyl)methanone(64357-69-3)

Safety Data

• Hazardous Substances Data: 64357-69-3(Hazardous Substances Data)

Usage

General Description

(4-cyclohexylphenyl)(phenyl)methanone, also known as 4-Cyclohexylbenzophenone, is a chemical compound with the molecular formula C19H18O. It is a white powder that is commonly used as a UV absorber in various plastics and polymer applications. (4-cyclohexylphenyl)(phenyl)methanone is also used as a photoinitiator in UV-curable inks and coatings. In addition, it has potential applications in the production of pharmaceuticals and agrochemicals. It is important to handle this chemical with care and to follow proper safety precautions when working with it.

Upstream product

• 629-27-6 1-Iodooctane 
• 72399-18-9 formaldehyde O-benzyloxime 
• 626-62-0 Cyclohexyl iodide 
• 97-63-2 methyl methacrylate 
• 558-17-8 tert-Butyl iodide 
• 90-90-4 (4-bromophenyl)(phenyl)methanone 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 140-88-5 ethyl acrylate 
• 153094-32-7 O,O'-bistributyltin benzopinacolate 
• 623-43-8 crotonic acid methyl ester 
• 4786-20-3 crotononitrile 
• 591-50-4 iodobenzene 
• 827-52-1 1-phenyl-1-cyclohexane 
• 98-88-4 benzoyl chloride 

Downstream Products

• 40231-37-6 1-(4-cyclohexyl-phenyl)-1-phenyl-ethene 
• 611-95-0 4-carboxybenzophenone 
• 72396-96-4 4-cyclohexyl-benzhydryl chloride 
• 860376-13-2 4-cyclohexyl-trityl chloride 
• 72396-97-5 4-Cyclohexyl-benzhydrol 
• 873381-46-5 (4-cyclohexylphenyl)diphenylmethanol 

Relevant articles and documents

Nickel-catalyzed C-N bond activation: Activated primary amines as alkylating reagents in reductive cross-coupling

Nickel-catalyzed reductive cross coupling of activated primary amines with aryl halides under mild reaction conditions has been achieved for the first time. Due to the avoidance of stoichiometric organometallic reagents and external bases, the scope regarding both coupling partners is broad. Thus, a wide range of substrates, natural products and drugs with diverse functional groups are tolerated. Moreover, experimental mechanistic investigations and density functional theory (DFT) calculations in combination with wavefunction analysis have been performed to understand the catalytic cycle in more detail.

BIS(TRI-n-BUTYLSTANNYL)BENZOPINACOLATE: PREPARATION AND USE AS A MEDIATOR OF INTERMOLECULAR FREE RADICAL REACTIONS

Bis(tri-n-butylstannyl)benzopinacolinate (2) serves as a thermal source of tri-n-butylstannyl radicals and mediates intermolecular coupling of selected alkyl halides to O-benzylformaldoxime and electron deficient olefins.A free radical non-chain mechanism is proposed for these reactions.