1654-05-3

Usage

Uses

Used in Fragrance Industry:
1-Penten-3-one, 4,4-dimethyl-1-(4-methylphenyl)is used as a fragrance ingredient for its sweet, minty, and citrus-like aroma. It is commonly used in perfumes, soaps, and other personal care products to provide a refreshing and pleasant scent.
Used in Flavor Industry:
1-Penten-3-one, 4,4-dimethyl-1-(4-methylphenyl)is used as a flavoring agent in food products. Its sweet, minty, and citrus-like aroma makes it suitable for enhancing the taste and aroma of various food items.
Used in Antimicrobial Applications:
1-Penten-3-one, 4,4-dimethyl-1-(4-methylphenyl)has been studied for its potential antimicrobial properties. It can be used as a natural preservative in food products and cosmetics to prevent the growth of harmful microorganisms.
Used in Antioxidant Applications:
1-Penten-3-one, 4,4-dimethyl-1-(4-methylphenyl)has also been studied for its potential antioxidant properties. It can be used in various industries, such as food and cosmetics, to protect products from oxidation and extend their shelf life.
Overall, 1-Penten-3-one, 4,4-dimethyl-1-(4-methylphenyl)is a versatile and valuable compound in the field of natural products chemistry and biochemistry, with a wide range of applications in various industries. It is considered safe for use in these applications when used in appropriate concentrations.

Upstream product

• 75-97-8 3,3-dimethyl-butan-2-one 
• 104-87-0 4-methyl-benzaldehyde 

Downstream Products

• 80618-73-1 2-tert-butyl-2-(4-methylstyryl)-oxirane 
• 698361-80-7 (Z)-2,2,8,8-Tetramethyl-5-p-tolyl-non-4-ene-3,7-dione 
• 97792-21-7 2,2,8,8-Tetramethyl-5-p-tolyl-nonane-3,7-dione 

Relevant academic research and scientific papers

Structure and Photophysical Properties of 2,6-Di-tert-Butyl-4-arylpyrylium 2-Naphthalenesulfonate Ion Pairs in Solution and in the Solid State

2,6-Di-tert-butyl-4-arylpyrylium 2-naphthalenesulfonate salts form ion pairs in dimethylcarbonate solution that exhibit charge-transfer absorptions and result in the rapid quenching of the pyrylium fluorescence.Molecular mechanics calculations predict that these ion pairs exist in a T-shaped orientation, but X-ray structural analysis reveals a ? face-to-face arrangement in the solid state.Nuclear Overhauser effect and time-resolved spectroscopic experiments carried out in solution are consistent with a T-shape for the ion pair, but these experiments do not prove that this structural hypothesis is correct.

I2-mediated oxidative C-N bond formation for metal-free one-pot synthesis of di-, tri-, and tetrasubstituted pyrazoles from α,β-unsaturated aldehydes/ketones and hydrazines

An I2-mediated metal-free oxidative C-N bond formation methodology has been established for the regioselective pyrazole synthesis. This practical and eco-friendly one-pot protocol requires no isolation of the less stable intermediates hydrazone

ANTIFUNGAL 1, 2, 4-TRIAZOLYL DERIVATIVES HAVING A 5- SULFUR SUBSTITUENT

The present invention relates to novel triazole compounds of the formulae (I) and (II) as defined below, to agricultural and pharmaceutical compositions containing them and to their use as fungicides, antimycotic, anticancer and antiviral agents.