3495-19-0

Usage

Uses

Used in Chemical Synthesis:
Ethanone, 1-(5-methyl-1,3-dioxan-5-yl)is used as a solvent and intermediate in the chemical synthesis industry for the production of various chemicals. Its versatile chemical properties make it a valuable component in the synthesis process.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Ethanone, 1-(5-methyl-1,3-dioxan-5-yl)is used as a key component in the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs and medications.
Used in Fragrance Industry:
Ethanone, 1-(5-methyl-1,3-dioxan-5-yl)is utilized in the fragrance industry for its fruity odor. It is used as a component in the creation of various perfumes, colognes, and other scented products.
Used in Food Industry:
In the food industry, Ethanone, 1-(5-methyl-1,3-dioxan-5-yl)is used as a flavoring agent to enhance the taste and aroma of various food products. Its fruity scent adds a pleasant flavor profile to a wide range of culinary applications.

Upstream product

• 50-00-0 formaldehyd 
• 6868-97-9 3-oxo-2,2-bis-(hydroxymethyl)butane 
• 7553-56-2 iodine 
• 78-93-3 butanone 

Downstream Products

• 144580-61-0 1-(5-methyl-[1,3]dioxan-5-yl)-ethanone-(2,4-dinitro-phenylhydrazone) 
• 114425-18-2 3-dibenzylamino-1-(5-methyl-[1,3]dioxan-5-yl)-propan-1-one 
• 132704-14-4 5-methyl-5-(α-methyl-α-hydroxyethyl)-1,3-dioxane 
• 20568-04-1 5-methyl-5-(α-hydroxyethyl)-1,3-dioxane 
• 6868-97-9 3-oxo-2,2-bis-(hydroxymethyl)butane 
• 171001-40-4 3-(4-chlorophenyl)-1-(5-methyl-1,3-dioxan-5-yl)prop-2-en-1-one 
• 91505-05-4 2,4-dichlorophenethenyl 5-methyl-1,3-dioxan-5-yl ketone 

Relevant academic research and scientific papers

Tandem bis-aldol reaction of ketones: A facile one-pot synthesis of 1,3-dioxanes in aqueous medium

(Chemical Equation Presented) A novel tandem bis-aldol reaction of ketone with paraformaldehyde catalyzed by polystyrenesulfonic acid in aqueous medium delivers 1,3-dioxanes in high yield. This one-pot, operationally simple microwave-assisted synthetic pr

Synthesis of dInaphtho[2,1-d, g][1,3] dioxocin derivatives from α,α-bishydroxymethyl-2-butanone

Ketoaldehydes which are formed in situ by the rearrangement of α,aα-Bishydroxymethyl-2-butanone in acidic medium, reacted with 2-naphthol. New dinaphtho[2,1-d,g][1,3] dioxocin derivatives were synthesized.

Heterocyclo-hydroxyalkyl-azolyl derivatives and use as fungicides

Heterocyclyl-hydroxyalkyl-azolyl derivatives of the formula STR1 in which Az represents 1,2,4-triazol-1-yl, 1,2,4-triazol-4-yl or imidazol-1-yl, Het represents optionally substituted dioxolanyl or 1,3-dioxanyl, R represents alkyl, optionally substituted p

Antimycotic agents

The invention concerns the provision of compound of Formula I as defined herein as well as compositions containing compound of Formula I. Said compounds and compositions are used as antimycotic agents and the invention includes such use.