22528-77-4

Basic information

• Product Name: Ethanone, 1-phenyl-2-(tetrahydro-2H-pyran-2-yl)-
• CAS NO: 22528-77-4
• Molecular Formula: C13H16O2
• Molecular Weight: 204.269
• Mol File: 22528-77-4.mol
• Article Data: 24

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-phenyl-2-(tetrahydro-2H-pyran-2-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-phenyl-2-(tetrahydro-2H-pyran-2-yl)-(22528-77-4)
• EPA Substance Registry System: Ethanone, 1-phenyl-2-(tetrahydro-2H-pyran-2-yl)-(22528-77-4)

Safety Data

• Hazardous Substances Data: 22528-77-4(Hazardous Substances Data)

Upstream product

• 1927-68-0 2-butoxytetrahydropyran 
• 98-86-2 acetophenone 
• 6581-66-4 2-methoxytetrahydropyran 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 34723-82-5 2-(bromomethyl)tetrahydro-2H-pyran 
• 1033861-42-5 C₁₅H₁₈O₃ 
• 1033862-14-4 C₁₅H₁₈O₃ 
• 142-68-7 TETRAHYDROPYRANE 
• 111-30-8 Glutaraldehyde 
• 20913-05-7 (Benzoylmethylene)triphenylphosphorane 
• 200624-55-1 7-oxo-7-phenylhept-5-enal 
• 57957-24-1 N-(1-phenylvinyl)acetamide 
• 621-82-9 Cinnamic acid 
• 1329464-93-8 7-phenylhept-6-yne-1,5-diol 

Downstream Products

• 383429-08-1 Acetic acid (E)-7-oxo-7-phenyl-hept-5-enyl ester 

Relevant articles and documents

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A new visible-light-promoted oxidative coupling of vinylarenes with cyclic ethers has been developed using rose bengal as photocatalyst and tert-butyl hydrogenperoxide (TBHP) as oxidant under ambient air at room temperature. A library of α-oxyalkylated ketones with broad functionalities has been synthesized in moderate to good yields. A radical mechanism is suggested for the present protocol.

Transition-Metal-Free Oxidative Decarboxylative Cross Coupling of α,β-Unsaturated Carboxylic Acids with Cyclic Ethers under Air Conditions: Mild Synthesis of α-Oxyalkyl Ketones

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Method for performing decarboxylated oxidative coupling on cinnamic acid derivatives and cyclic ethers

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