64357-69-3

Usage

Uses

Used in Plastics and Polymer Industry:
(4-cyclohexylphenyl)(phenyl)methanone is used as a UV absorber for protecting plastics and polymers from the harmful effects of ultraviolet radiation, thereby enhancing their durability and stability.
Used in Printing and Coating Industry:
(4-cyclohexylphenyl)(phenyl)methanone is used as a photoinitiator in UV-curable inks and coatings, enabling rapid curing and providing excellent adhesion and durability.
Used in Pharmaceutical and Agrochemical Industry:
(4-cyclohexylphenyl)(phenyl)methanone has potential applications in the production of pharmaceuticals and agrochemicals, where it can be utilized as an intermediate or a key component in the synthesis of various active ingredients.
It is important to handle this chemical with care and to follow proper safety precautions when working with it.

Upstream product

• 827-52-1 1-phenyl-1-cyclohexane 
• 98-88-4 benzoyl chloride 
• 591-50-4 iodobenzene 
• 72399-18-9 formaldehyde O-benzyloxime 
• 629-27-6 1-Iodooctane 
• 4786-20-3 crotononitrile 
• 626-62-0 Cyclohexyl iodide 
• 153094-32-7 O,O'-bistributyltin benzopinacolate 
• 558-17-8 tert-Butyl iodide 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 90-90-4 (4-bromophenyl)(phenyl)methanone 
• 136-01-6 cyclohexanecarboxylic acid Na-salt 
• 6136-66-9 4-iodobenzophenone 
• 140-88-5 ethyl acrylate 

Downstream Products

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

Relevant academic research and scientific papers

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.

One-Pot Electrochemical Nickel-Catalyzed Decarboxylative Sp2-Sp3 Cross-Coupling

A one-pot electrochemical nickel-catalyzed decarboxylative sp2-sp3 cross-coupling reaction has been developed using redox-active esters prepared in situ from alkyl carboxylates and N-hydroxyphthalimide tetramethyluronium hexafluorophosphate (PITU). This undivided cell one-pot method enables C-C bond formation using inexpensive, benchtop-stable reagents with isolated yields up to 95% with good functional group tolerance, which includes nitrile, ketone, ester, alkene and selectivity over other aromatic halogens.

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.