4-(Trifluoromethoxy)phenylacetylene is an organic compound characterized by its distinctive functional groups and structure. It features a phenyl ring substituted with a trifluoromethoxy group and an acetylene moiety. The presence of the trifluoromethoxy group imparts unique electronic properties, enhancing the compound's reactivity and potential applications in various chemical reactions, particularly in organic synthesis and materials science. This compound is typically a colorless to pale yellow liquid or solid, depending on its state at room temperature. Its molecular structure contributes to its hydrophobic nature, making it less soluble in water but soluble in organic solvents. The trifluoromethoxy group also influences its thermal stability and volatility. Due to its unique characteristics, 4-(trifluoromethoxy)phenylacetylene may be utilized in the development of pharmaceuticals, agrochemicals, or as an intermediate in the synthesis of more complex organic molecules. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested.

4-(TRIFLUOROMETHOXY)PHENYLACETYLENE

160542-02-9: 4-Ethynyl-1-(Trifluoromethoxy) Benzene, 1-Ethynyl-4-(Trifluoromethoxy)-Benzene

Benzene, 1-ethynyl-4-(trifluoromethoxy)-

4-(Trifluoromethoxy)phenylacetylene

1-Ethynyl-4-(trifluoromethoxy)benzene is a fluorescent probe that can be used for detection of azide in human serum.

CAS 160542-02-9: 4-(TRIFLUOROMETHOXY)PHENYLACETYLENE

Benzene, 1-ethynyl-4-(trifluoromethoxy)-

Ref: IN-DA001S0S

4-(Trifluoromethoxy)phenylacetylene

Ref: 54-PC5952

1-Ethynyl-4-(Trifluoromethoxy)Benzene

Ref: 3D-FE83659

1-Ethynyl-4-(trifluoromethoxy)benzene

Ref: 3B-E1170

4-(Trifluoromethoxy)phenylacetylene

Ref: 10-F046090