67091-10-5

Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 1-[2-hydroxy-4-(2-propynyloxy)phenyl]is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of new drug molecules with potential therapeutic applications.
Used in Dye Industry:
Ethanone, 1-[2-hydroxy-4-(2-propynyloxy)phenyl]is used as a key component in the production of dyes. Its chemical properties enable the creation of a wide range of colors, making it a valuable asset in the dye industry.
Used in Flavor Industry:
Ethanone, 1-[2-hydroxy-4-(2-propynyloxy)phenyl]is used as a flavoring agent in the food and beverage industry. Its unique aroma profile can be used to enhance the taste of various products.
Used in Research and Experimental Settings:
Ethanone, 1-[2-hydroxy-4-(2-propynyloxy)phenyl]is used as a research compound in various scientific studies. Its properties make it a valuable tool for understanding chemical reactions and exploring new areas of research.
Used in Medicine and Biotechnology:
Ethanone, 1-[2-hydroxy-4-(2-propynyloxy)phenyl]is used as a potential therapeutic agent in the field of medicine and biotechnology. Its unique structure may offer new opportunities for the development of novel treatments and therapies.
Used in Industrial Processes and Manufacturing:
Ethanone, 1-[2-hydroxy-4-(2-propynyloxy)phenyl]is used in various industrial processes and manufacturing applications. Its versatility and chemical properties make it a valuable component in the production of a wide range of products.

Upstream product

• 108-46-3 recorcinol 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 6165-76-0 propargyl p-toluenesulfonate 
• 624-65-7 2-propynyl chloride 
• 106-96-7 propargyl bromide 

Relevant academic research and scientific papers

Synthesis and Cytotoxicity of Chalcone Based 1,2,3-Triazole Derivatives

Abstract: Synthesis of a novel series of chalcone based 1,2,3-triazole derivatives and their anti-cancer studies are presented. Majority of the target compounds exhibit moderate to excellent activity against A-549 cells. Among the compounds screened 7c an

Tryptamine–Triazole Hybrid Compounds for Selective Butyrylcholinesterase Inhibition

Tryptamine–triazole hybrid compounds (11–18) were synthesized via click reaction between tryptamine azide and propargylated natural compounds. Their cholinesterase inhibitory activity was evaluated. Among the eight compounds, compound 11 showed the most p

Synthesis and Antibacterial Activity of Some {6-[(1H-1,2,3-Triazol-4-yl)methoxy]-3-methylbenzofuran-2-yl}(4-bromophenyl)methanone Derivatives

A series of novel benzofuran?1,2,3-triazole hybrid heterocyclic molecules were synthesized using a click chemistry approach. The structure of the synthesized compounds was assessed by IR and NMR spectroscopy and mass spectrometry. The products showed moderate to high activity against gram-positive and gram-negative bacteria.

A tryptamine-paeonol hybridization compound inhibits LPS-mediated inflammation in BV2 cells

In the present study, we synthesized and evaluated the anti-inflammatory effects of three tryptamine (Trm) hybrid compounds, HBU-375, HBU-376 and HBU-379. The Click reaction between the azido-Trm and 2- or 4-propazylated paeonol moiety resulted in HBU-376

Synthesis and antimicrobial activity of some novel benzofuran based 1,2,3-triazoles

In the present study, a series of novel {6-[(1H-1,2,3-triazol-4-yl)methoxy]-3-methylbenzofuran-2-yl}(phenyl)methanones (7a–7o) have been synthesized using click chemistry approach. The structures of all newly synthesized compounds were characterized by FT-IR, 1H and 13C NMR, and MASS spectral data. Most of products demonstrated high antimicrobial activity.

Microwave-assisted synthesis, molecular docking and antimicrobial activity of novel 2-(3-aryl,1-phenyl-1H-pyrazol-4-yl)-8H-pyrano[2,3-f]chromen-4-ones

An efficient synthetic protocol of microwave-assisted synthesis of some novel 2-(3-aryl,1-phenyl-1H-pyrazol-4-yl)-8H-pyrano[2,3-f]chromen-4-ones 6a-j in excellent yields starting from 3-(3-aryl,1-phenyl-1H-pyrazol-4-yl)-1-(5-hydroxy-2H-chromen-6-yl)-prope

An uracil-linked hydroxyflavone probe for the recognition of ATP

Background: Nucleotides are essential molecules in living systems due to their paramount importance in various physiological processes. In the past years, numerous attempts were made to selectively recognize and detect these analytes, especially ATP using

Synthesis, spectroscopy, X-ray crystallography, DFT calculations, DNA binding and molecular docking of a propargyl arms containing Schiff base

A propargyl arms containing Schiff base (L) was synthesized by the condensation of 1-[2-hydroxy-4-(prop-2-yn-1-yloxy)phenyl]ethanone with trans-1,2-diaminocyclohexane. The structure of L was characterized by IR, 1H NMR, 13C NMR and U

Synthesis and Antibacterial Evaluation of Benzofuran Based Di-1,2,3-triazoles

A series of novel benzofuran-1,2,3-triazole hybrid molecules are synthesized using the click chemistry approach. Structures of the synthesized compounds were assessed by IR, NMR, and mass spectroscopy. The tests of final products 10a–10l for their antibacterial activity demonstrate excellent to good activity against gram-positive and gram-negative bacteria.

Design and Synthesis of Antimicrobial Active (E)-(3-(Substituted-styryl)-7H-furo[2,3-f]chromen-2-yl)(phenyl)methanone Derivatives and Their In Silico Molecular Docking Studies

Nine new (E)-(3-(substituted-styryl)-7H-furo[2,3-f]chromen-2-yl)(phenyl)methanone derivatives, 7(a–i), with an efficient microwave-assisted synthetic method was achieved by reacting with (E)-3-(aryl)-1-(5-hydroxy-2H-chromen-6-yl)prop-2-en-1-ones and 2-bro