7473-97-4

Usage

Physical appearance

Pale yellow liquid the compound has a light yellow color and is in a liquid state at room temperature.

Odor

Slight odor the compound has a very faint smell, which may not be easily noticeable.

Solubility

Insoluble in water, soluble in organic solvents the compound does not dissolve well in water but dissolves easily in certain organic solvents.

Uses

Flavoring agent, fragrance ingredient, pharmaceutical intermediate the compound is commonly used in the food, cosmetic, and pharmaceutical industries for its various properties.

Potential applications

Antioxidant, antimicrobial agent 1-methoxy-1,1-diphenylpropan-2-one has been studied for its possible use in preventing oxidation and inhibiting the growth of microorganisms.

Safety precautions

Handle with care it is important to follow proper safety measures when working with 1-methoxy-1,1-diphenylpropan-2-one to avoid potential hazards.

Upstream product

• 67-56-1 methanol 
• 33609-25-5 3-bromo-1,1-diphenylpropan-2-one 
• 33718-91-1 1,1-diphenyl-1-bromo-2-propanone 
• 917-64-6 methyl magnesium iodide 
• 19481-81-3 (α-diphenylmethyl)cyano chloride 
• 125288-37-1 2,2,-diphenyl-2-methoxyethanenitrile 
• 86-29-3 Diphenylacetonitrile 
• 781-35-1 1,1-diphenylacetone 

Downstream Products

• 7474-01-3 1-methoxy-2-methyl-1,1-diphenyl-propan-2-ol 
• 130821-79-3 1-methoxy-1,1-diphenyl-propan-2-ol 
• 110-91-8 morpholine 
• 1076068-47-7 C₁₇H₁₅F₃O₄S 
• 28193-21-7 1,1-Diphenyl-1-methoxy-3-dimethylamin-propan-2-on hydrochlorid 

Relevant academic research and scientific papers

Rhodium-catalyzed hydroalkynylation of internal alkynes with silylacetylenes: An alkynylrhodium(I) intermediate generated from the hydroxorhodium(I) complex [Rh(OH)(binap)]2

A highly selective hydroalkynylation of internal alkynes with silylacetylenes giving 1,3-enynes was realized by use of a hydroxorhodium catalyst. As a key intermediate in the catalytic cycle, an alkynylrhodium(I) complex was isolated and investigated for its structure and reactivity.

The synthesis of some 1,1-diphenyl-1-alkoxy-3-alkylamino-2-propanones''' of biological interest

The synthesis of 1,1-diphenyl-1-alkoxy-3-alkylamino-2-propanones is reported. For this synthesis the following series of reactions was utilized: 1-phenyl-1-propanone was brominated, the product reacted with benzene (Friedel-Crafts), the 1,1-diphenyl-3-propanone was brominated, then reacted with the appropriate alcohol, the alkoxy derivative was brominated and then reacted with the appropriate amine. The synthesized compounds were tested for analgesic activity. All test compounds showed weak analgesic action, the most active were 1,1-diphenyl-1-ethoxy-3-piperidino-2-propanone and 1,1-diphenyl-1-phenoxy-3-dimethylamino-2-propanone.