15074-16-5

Usage

Uses

Used in Pharmaceutical Synthesis:
1-(2-hydroxyphenyl)-4-phenylbutan-1-one is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic benefits.
Used as a Flavoring Agent in Food and Beverages:
In the food and beverage industry, 1-(2-hydroxyphenyl)-4-phenylbutan-1-one is used as a flavoring agent to enhance the taste and aroma of various products, capitalizing on its chemical properties to create desirable flavors.
Used in Cancer Research:
1-(2-hydroxyphenyl)-4-phenylbutan-1-one is used as a potential chemo-preventive agent in cancer research due to its demonstrated antioxidant and anti-inflammatory properties. Studies have shown that it may have anti-cancer activity, making it a subject of interest for further investigation into its role in cancer treatment and prevention.
Used in Antioxidant and Anti-inflammatory Applications:
1-(2-hydroxyphenyl)-4-phenylbutan-1-one is also used in the development of products with antioxidant and anti-inflammatory properties, leveraging its identified benefits in these areas to contribute to the health and wellness industry.

Upstream product

• 98-85-1 1-Phenylethanol 
• 118-93-4 o-hydroxyacetophenone 
• 51552-98-8 3-phenylbutanoyl chloride 

Relevant academic research and scientific papers

Synthesis and structural characterization of facile ruthenium(II) hydrazone complexes: Efficient catalysts in α-alkylation of ketones with primary alcohols via hydrogen auto transfer

As a immersion for development of new complexes, new Ru(II) complexes (1–3) supported by benzothiazole hydrazine Schiff bases of the type [Ru(SAL-HBT)(CO)(AsPh3)2], [Ru(VAN-HBT)(CO)(AsPh3)2] and [Ru(NAP-HBT)(CO)Cl(AsPh3)2] [SAL-HBT = (salicyl((2-(benzothiazol-2yl)hydrazono)methylphenol)), VAN-HBT = 2-((2-(benzothiazol-2-yl)hydrazono)methyl)-6 methoxyphenol) and NAP-HBT = naphtyl-2-((2-(benzothiazol-2-yl)hydrazono)methyl phenol)] were synthesized. Their identities have been established by satisfactory elemental analyses, various spectroscopic techniques (IR, (1H, 13C) NMR) and also mass spectrometry. The ruthenium(II) ion exhibits a hexa coordination with distorted octahedral geometry. In complexes 1 and 2, the ligand coordinated as dianionic tridentate fashion by forming N^N donor five member and N^O donor six member chelate rings. However, in complex 3, the ligand coordinated as monoanionic bidentate fashion by forming N^N donor five-membered ring. The new ruthenium(II) carbonyl complexes were successfully applied as catalysts in α -alkylation of aliphatic and aromatic ketones with alcohols via borrowing hydrogen strategy. Various parameters such as base, solvent, temperature, time and catalyst loading on the catalytic activity were analyzed. From the results, the catalyst 1 was found to be the best catalyst for α-alkylation reaction to obtain excellent yield. The catalytic system has a broad substrate scope, which allows the synthesis of α-alkylated ketones in mild reaction conditions with low catalyst loading under air atmosphere.

Organic compounds

Disclosed are certain compounds according to the general formula (I) and their use as flavoring and fragrancing compounds, as well as fragranced and flavored compositions comprising the compounds of formula (I), and methods for providing a flavor or fragrance to compositions and articles utilizing the compounds of formula (I).