2,2,2-Trifluoro-1-naphthalen-2-ylethanone, with the CAS number 1800-42-6, is an organic compound characterized by its unique structure, which includes a naphthalene ring substituted with a trifluoroethyl group and a ketone functional group. This compound typically exhibits a high degree of lipophilicity due to the presence of the naphthalene moiety, which can influence its solubility in organic solvents. The trifluoromethyl group contributes to its chemical stability and can enhance its reactivity in certain chemical reactions, particularly in electrophilic aromatic substitution. Additionally, the presence of fluorine atoms often imparts distinctive physical properties, such as increased volatility and altered boiling and melting points compared to non-fluorinated analogs. 2,2,2-Trifluoro-1-naphthalen-2-ylethanone may find applications in various fields, including pharmaceuticals and agrochemicals, due to its potential as an intermediate in synthetic pathways. Safety data should be consulted for handling and usage, as fluorinated compounds can exhibit unique toxicological profiles.

2,2,2-trifluoro-1-naphthalen-2-ylethanone

1800-42-6: 2,2,2-Trifluoro-1-naphthalen-2-ylethanone, with the CAS number 1800-42-6, is an organic compound characterized by its unique structure, which includes a naphthalene ring substituted with a trifluoroethyl group and a ketone functional group. This compound typically exhibits a high degree of lipophilicity due to the presence of the naphthalene moiety, which can influence its solubility in organic solvents. The trifluoromethyl group contributes to its chemical stability and can enhance its reactivity in certain chemical reactions, particularly in electrophilic aromatic substitution. Additionally, the presence of fluorine atoms often imparts distinctive physical properties, such as increased volatility and altered boiling and melting points compared to non-fluorinated analogs. 2,2,2-Trifluoro-1-naphthalen-2-ylethanone may find applications in various fields, including pharmaceuticals and agrochemicals, due to its potential as an intermediate in synthetic pathways. Safety data should be consulted for handling and usage, as fluorinated compounds can exhibit unique toxicological profiles.

CAS 1800-42-6

2,2,2-trifluoro-1-naphthalen-2-ylethanone

Ethanone, 2,2,2-trifluoro-1-(2-naphthalenyl)-

Ref: IN-DA0021LE

2,2,2-Trifluoro-1-(naphthalen-2-yl)ethan-1-one

Ref: 54-PC101281

2-Trifluoroacetylnaphthalene

Ref: 10-F207029