1-Ethynyl-2-(trifluoromethoxy)benzene, with the CAS number 886363-40-2, is an organic compound characterized by its unique functional groups and structure. It features a benzene ring substituted with an ethynyl group and a trifluoromethoxy group, which significantly influences its chemical properties. The presence of the ethynyl group introduces a triple bond, making it a terminal alkyne, while the trifluoromethoxy group enhances its electron-withdrawing characteristics due to the electronegativity of the fluorine atoms. This compound is likely to exhibit hydrophobic behavior due to the aromatic nature of the benzene ring and the presence of the trifluoromethoxy group, which can also impart unique reactivity in various chemical reactions, such as nucleophilic substitutions or coupling reactions. Additionally, the trifluoromethoxy group can affect the compound's solubility and stability in different solvents. Overall, 1-ethynyl-2-(trifluoromethoxy)benzene is of interest in organic synthesis and materials science due to its distinctive structural features and potential applications in pharmaceuticals and agrochemicals.

1-ethynyl-2-(trifluoromethoxy)benzene

886363-40-2: 2-Ethynylphenyl trifluoromethyl ether, Benzene, 1-Ethynyl-2-(Trifluoromethoxy)-

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CAS 886363-40-2: 1-ethynyl-2-(trifluoromethoxy)benzene

2'-Trifluoromethoxyphenyl acetylene

Ref: 3D-FT82609

2-(Trifluoromethoxy)phenylacetylene

Ref: 54-PC53008

1-Ethynyl-2-(trifluoromethoxy)benzene

Ref: IN-DA00GSM8

2'-TRIFLUOROMETHOXYPHENYL ACETYLENE

Ref: 10-F305902