34264-13-6

Basic information

• Product Name: 1-(3-(prop-2-yn-1-yloxy)phenyl)ethan-1-one
• Synonyms: 1-(3-(prop-2-yn-1-yloxy)phenyl)ethan-1-one
• CAS NO: 34264-13-6
• Molecular Weight: 174.199
• Mol File: 34264-13-6.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1-(3-(prop-2-yn-1-yloxy)phenyl)ethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-(prop-2-yn-1-yloxy)phenyl)ethan-1-one(34264-13-6)
• EPA Substance Registry System: 1-(3-(prop-2-yn-1-yloxy)phenyl)ethan-1-one(34264-13-6)

Safety Data

• Hazardous Substances Data: 34264-13-6(Hazardous Substances Data)

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 articles and documents

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

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

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