6477-28-7

Usage

Ketone derivative

Structure 1-phenyl-3-(2,4,6-trimethylphenyl)propane-1,3-dione is a derivative of a ketone, which is a class of organic compounds with a carbonyl functional group (C=O) bonded to two carbon atoms.

Key intermediate

Synthesis 1-phenyl-3-(2,4,6-trimethylphenyl)propane-1,3-dione serves as a crucial intermediate in the synthesis of various important organic compounds, making it valuable in chemical research and production.

Applications

Pharmaceutical, agrochemical, and fragrance industries 1-phenyl-3-(2,4,6-trimethylphenyl)propane-1,3-dione is widely used in the production of pharmaceuticals, agrochemicals, and fragrances due to its versatile chemical properties.

Physical form

Yellowish to greenish crystalline powder The compound appears as a yellowish to greenish crystalline powder, which is a common form for many organic compounds.

Solubility

Insoluble in water, soluble in organic solvents 1-phenyl-3-(2,4,6-trimethylphenyl)propane-1,3-dione does not dissolve in water but can dissolve in many organic solvents, such as ethanol or acetone.

Hazardous nature

Potentially hazardous, strict safety protocols 1-phenyl-3-(2,4,6-trimethylphenyl)propane-1,3-dione is potentially hazardous, and it is essential to handle it with care and follow strict safety protocols to minimize risks to human health and the environment.

Upstream product

• 854651-26-6 2-bromo-1-mesityl-3-phenyl-propane-1,3-dione 
• 127-08-2 potassium acetate 
• 64-19-7 acetic acid 
• 93-89-0 benzoic acid ethyl ester 
• 1667-01-2 2,4,6-Trimethylacetophenone 
• 7664-93-9 sulfuric acid 
• 5689-92-9 3-(2,4,6-trimethylphenyl)-1-phenylprop-2-yn-1-one 
• 7647-01-0 hydrogenchloride 
• 67-56-1 methanol 
• 855174-52-6 β-methoxy-2,4,6-trimethyl-chalcone 
• 37975-16-9 1-(3-nitrophenyl)-3-(4-methoxyphenyl)propane-1,3-dione 

Downstream Products

• 80651-61-2 3-phenyl-1-mesitoyl-2-buten-1-one 
• 102750-84-5 1-mesityl-3,3-diphenylprop-2-en-1-one 
• 855174-52-6 β-methoxy-2,4,6-trimethyl-chalcone 
• 854901-29-4 mesityl-phenyl-propanetrione 
• 854651-26-6 2-bromo-1-mesityl-3-phenyl-propane-1,3-dione 
• 24074-20-2 3-phenyl-5-(2,4,6-trimethyl-phenyl)-isoxazole 
• 42797-62-6 2-Diazo-1-phenyl-3-(2,4,6-trimethylphenyl)-1,3-propandion 
• 146918-54-9 3-hydroximino-1-mesityl-3-phenylpropan-1-one 
• 1667-01-2 2,4,6-Trimethylacetophenone 
• 100-52-7 benzaldehyde 
• 1391054-99-1 C₂₁H₂₄O₂ 
• 104550-18-7 (Z)-3-Hydroxy-3-phenyl-2-(2,4,6-trimethylphenyl)-2-propensaeure-tert-butylester 
• 104550-19-8 (Z)-3-Hydroxy-2-phenyl-3-(2,4,6-trimethylphenyl)-2-propensaeure-ethylester 
• 107626-95-9 3-phenyl-1-(2,4,6-trimethylphenyl)-1-propanone 

Relevant academic research and scientific papers

On the Oximation of Diaryl-β-diketones

The reaction of asymmetrically substituted β-diketones with hydroxylamine to give 3,5-diarylisoxazoles has been re-investigated, and has been found to occur with a low degree of site-selectivity unless steric effects are operating.The isoxazole that has t

Synthesis of dibenzoylmethane derivatives and inhibition of mutagenicity in Salmonella typhimurium

Twenty dibenzoylmethanes with methyl, methoxy, bromo, chloro, or fluoro substitution on either one or both benzene rings were synthesized and assayed for inhibition of the mutagenicity of 2-nitrofluorene in S. typhimurium TA98. 2,2-Dimethoxy, 3,3-dimethoxy and 3,3,4,4-tetramethoxydibenzoylmethane was as active as dibenzoylmethane. None of the halogen-substituted dibenzoylmethanes were active. These results demonstrate that dibenzoylmethanes can inhibit the mutagenicity of 2-nitrofluorene, and that modifications made on the benzene rings of dibenzoylmethane cannot enhance the antimutagenicity of this parent compound.