4366-28-3

Basic information

• Product Name: 2-bromomethyl-2-(4-methoxyphenyl)-1,3-dioxolane
• Synonyms: 2-bromomethyl-2-(4-methoxyphenyl)-1,3-dioxolane
• CAS NO: 4366-28-3
• Molecular Weight: 273.126
• Mol File: 4366-28-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-bromomethyl-2-(4-methoxyphenyl)-1,3-dioxolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromomethyl-2-(4-methoxyphenyl)-1,3-dioxolane(4366-28-3)
• EPA Substance Registry System: 2-bromomethyl-2-(4-methoxyphenyl)-1,3-dioxolane(4366-28-3)

Safety Data

• Hazardous Substances Data: 4366-28-3(Hazardous Substances Data)

Upstream product

• 107-21-1 ethylene glycol 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 36881-00-2 2-(4-methoxyphenyl)-2-methyI-1,3-dioxolane 

Downstream Products

• 60233-15-0 1-((2-(4-methoxyphenyl)-1,3-dioxolane-2-yl)methyl)-1H-1,2,4-triazole 
• 80336-89-6 2-Bromoethyl 2-(4-methoxyphenyl)acetate 
• 101108-45-6 diethyl-[2-(4-methoxy-phenyl)-[1,3]dioxolan-2-ylmethyl]-amine 
• 114166-15-3 1-[2-(4-methoxy-phenyl)-[1,3]dioxolan-2-ylmethyl]-piperidine 

Relevant articles and documents

Propiconazole-like compound, and preparation method and application thereof

The invention discloses a propiconazole-like compound, and a preparation method and application thereof. The structural formula of the propiconazole-like compound is represented by formula (I)shown in the specification. In the formula (I), X is H, bromine

A Lewis Acid Catalyzed 1,2 Aryl Shift in α-Haloalkyl Aryl Acetals: A Convenient Route to α-Arylalkanoic Acids

A new method for the synthesis of α-arylalkanoic acids is given, based on Lewis acid promoted rearrangement of acetals of primary and secondary α-haloalkyl aryl ketones (halo = Br, Cl) in hydrocarbon solvents.The reaction is selective, providing the esters of α-arylalkanoic acids in almost quantitative yields.The ability of "soft and borderline" Lewis acids in activating the carbon-halogen bond is compared with that of silver salts.The reaction mechanism is discussed.The present synthesis has been applied to some α-arylpropionic acids well-known as antiinflammatory drugs.