64545-28-4

Usage

Phenyl group

Aromatic ring structure (C6H5) attached to a carbon atom.

Prop-2-en-1-one group

A three-carbon chain with a carbonyl group (C=O) at the end and a double bond between the first and second carbon atoms.

2,4,6-Trimethylphenyl group

A phenyl group with three methyl (CH3) groups attached to the 2nd, 4th, and 6th carbon positions.

Carbonyl group

A double-bonded oxygen atom (O=C) that is part of the ketone functional group.

Bonded to two carbon atoms

The carbonyl group is bonded to two carbon atoms, forming the ketone functional group.

Organic synthesis

The compound is commonly used as a key intermediate in the production of various other compounds.

Medicinal and pharmaceutical chemistry

The unique structure and functional groups make the compound valuable in the field of creating new medicines.

Flavors and fragrances

The compound is also used in the creation of flavors and fragrances.

Upstream product

• 487-68-3 mesytaldehyde 
• 98-86-2 acetophenone 

Downstream Products

• 1146963-11-2 amino[3-phenyl-5-(2,4,6-trimethylphenyl)-2-pyrazolin-1-yl]methane-1-thione 
• 1438279-07-2 (S)-3-(1H-indol-3-yl)-3-mesityl-1-phenylpropan-1-one 
• 133039-10-8 2,4,6-trimethyl-1-(3-phenyl-2-propen-1-yl)benzene 
• 95465-71-7 3-(2,4,6-trimethylphenyl)-1-phenylpropan-1-one 
• 1116338-35-2 C₂₁H₂₀N₂O 

Relevant academic research and scientific papers

Direct Reduction of Allylic Alcohols Using Isopropanol as Reductant

The lithium cation-catalyzed direct reduction of allylic alcohols to alkenes using isopropanol as a hydride donor was developed. The hydride transfer of the in situ-generated lithium isopropoxide to an allylic cation is the key process in this transformation. The reaction generates only water and acetone as byproducts, which highlights the synthetic utility of this method. (Figure presented.).

Conformationally restricted aza-dipyrromethene boron difluorides (aza-BODIPYs) with high fluorescent quantum yields

A simple approach to the highly fluorescent near-infrared aza-BODIPY dyes with higher fluorescence quantum yields (up to 0.81 in toluene) in comparison with their known analogues is presented. Our approach is based on the restricted rotations of the 1,7-p

Synthesis of new 2-(5-substituted-3-phenyl-2-pyrazolinyl)-1,3-thiazolino[5,4-b]quinoxaline derivatives and evaluation of their antiamoebic activity

In an effort to develop potent antiamoebic agents, we have synthesized chalcones (1-8), amino-5-substituted-(3-phenyl(2-pyrazolinyl))methane-1-thione derivatives (1a-8a) and 2-(5-substituted-3-phenyl-2-pyrazolinyl)-1,3-thiazolino[5,4-b]quinoxaline derivat

Aryliminodimagnesium Reagents. VI. The Reactions with Conjugated Carbonyl Compounds. The Initial Coordination and the Electron-transfer in the Reactions of Organomagnesium Reagents

The reactions of aryliminodimagnesium reagents (ArN(MgBr)2) with benzylideneacetophenones, quinones, and benzils were examined.Among the product-distributions in the reactions with the enones and the α-diketones, some examples in which p-MeO-substituted s