34264-13-6

Usage

Explanation

The compound is composed of 11 carbon atoms, 10 hydrogen atoms, and 2 oxygen atoms.

Explanation

The compound has a carbonyl group (C=O) as part of its structure, classifying it as a ketone.

Explanation

The compound contains a phenyl ring (C6H5) connected to an ethanone group (CH3C(O)-).

Explanation

A prop-2-yn-1-yloxy group (C3H5O) is attached to the 3rd carbon of the phenyl ring.

Explanation

The compound's reactivity allows it to be used in various chemical reactions, making it valuable in the synthesis of complex organic molecules and pharmaceutical compounds.

Explanation

The compound's structure and reactivity suggest that it could have potential applications in the development of new medications.

Explanation

Due to its structure and reactivity, the compound can serve as a building block for the synthesis of more complex organic molecules.

Explanation

The compound's properties make it a valuable tool for researchers studying various chemical reactions and mechanisms, helping to advance the understanding of organic chemistry.

Chemical structure

Ketone derivative

Phenyl ring

Attached to an ethanone group

Prop-2-yn-1-yloxy substituent

Located at the 3-position of the phenyl ring

Versatile reactivity

Used in organic synthesis and pharmaceutical research

Potential pharmacological properties

May be utilized in the development of new drugs

Building block

Can be used as a component in complex organic molecules

Research tool

Used in the study of chemical reactions and mechanisms

Upstream product

• 121-71-1 3-Hydroxyacetophenone 
• 106-96-7 propargyl bromide 

Downstream Products

• 1227420-54-3 3-(4-methoxy-phenyl)-1-(3-prop-2-ynyloxy-phenyl)-propenone 
• 1227420-55-4 3-(2,4-dimethoxy-phenyl)-1-(3-prop-2-ynyloxy-phenyl)-propenone 
• 1227420-56-5 1-(3-prop-2-ynyloxy-phenyl)-3-(2,3,4-trimethoxy-phenyl)-propenone 

Relevant academic research and scientific papers

Chalcomer assembly of optical chemosensors for selective Cu2+ and Ni2+ ion recognition

The o-, m- and p-isomeric units of chalconyl triazole-based, caged organosilicon complexes were efficiently synthesized and explored for their cationic chemosensing activities. The UV-vis spectral studies performed show considerable variations in absorpti

Unravelling the potency of triazole analogues for inhibiting α-synuclein fibrillogenesis andin vitrodisaggregation

A series of triazole-based compounds was synthesized using a click chemistry approach and evaluated for the inhibition of α-synuclein (α-syn) fibrillogenesis and its disaggregation. CompoundsTr3,Tr7,Tr12,Tr15, andTr16exhibited good effect in inhibiting α-

Heteroaryl chalcone allied triazole conjugated organosilatranes: Synthesis, spectral analysis, antimicrobial screening, photophysical and theoretical investigations

A series of heteroaryl tethered triazole conjoined organosilatranes were synthesized following an archetypal click reaction. The reaction sequence follows the initial generation of acetylinic Schiff bases (3a-3c, 4a-4c) which undergo 3 + 2 cycloaddition w

Molecular docking studies on COVID-19 and antibacterial evaluation of newly synthesized 4-(methoxymethyl)-1,2,3-triazolean analogues derived from (E)-1-phenyl-3-(2-(piperidin-1-yl)quinolin-3-yl) prop-2-en-1-one

A series of novel quinolone-based 4-(methoxymethyl)-1,2,3-triazole derivatives were synthesized, and their structures were characterized by 1H, 13C NMR and mass spectroscopy. The compounds (IXa-l) were screened in vitro antibacterial

Dipropargyl substituted diphenylpyrimidines as dual inhibitors of monoamine oxidase and acetylcholinesterase

Alzheimer's disease (AD) is a multifactorial neurological disorder involving complex pathogenesis. Single target directed drugs proved ineffective and since last few years' different pharmacological strategies including multi-targeting agents are being ex

Design, synthesis and biological evaluation of chalconyl blended triazole allied organosilatranes as giardicidal and trichomonacidal agents

A series of chalconyl blended triazole allied silatranes (7a-g/8a-g/9a-g) were synthesized in good yields using a simple, economical and biocompatible synthetic route. The blend of three different pharmacologically active moieties into a single scaffold r

Synthetic investigations and photo-physical properties of 1,2,3-triazole encapped chalconyl substituted organotriethoxysilanes

Organotriethoxysilanes (OTES) play an impressive role in the designing of organic-inorganic hybrid materials. The highly efficient copper catalysed 'Click Silylation' is followed for the functionalization of 3-azidopropyltriethoxysilane (AzPTES) with a se

Synthetic approach towards 'click' modified chalcone based organotriethoxysilanes; UV-Vis study

The efficient linkage of a conjugate chalcone to n-propyltriethoxysilanes (nPTES) via a 1,2,3-triazole with good yields is reported. The synthesis involves a Claisen-Schmidt condensation reaction followed by a copper(i) catalyzed azide-alkyne cycloadditio

Microwave-assisted copper azide alkyne cycloaddition (CuAAC) reaction using D-glucose as a better alternative reductant

D-Glucose has been established as a reducing agent for the copper azide alkyne cycloaddition (CuAAC) reactions. Efficacy of this new reductant has been established against various phenyl acetylenes (14 examples) and aryl azides (16 examples). All reaction

Synthesis, antimalarial and antitubercular activity of acetylenic chalcones

A series of acetylenic chalcones were evaluated for antimalarial and antitubercular activity. The antimalarial data for this series suggests that growth inhibition of the W2 strain of Plasmodium falciparum can be imparted by the introduction of a methoxy