1-(3-(Trifluoromethoxy)phenyl)-1H-pyrazole-4-carbaldehyde is a chemical compound characterized by its unique structural features, which include a pyrazole ring and a trifluoromethoxy group. The presence of the trifluoromethoxy substituent enhances its lipophilicity and may influence its reactivity and biological activity. This compound typically exhibits properties associated with aldehydes, such as being a reactive electrophile due to the carbonyl group, which can participate in various chemical reactions, including nucleophilic additions. The pyrazole moiety contributes to its potential as a pharmacophore in medicinal chemistry, as pyrazoles are often found in biologically active compounds. Additionally, the compound may display interesting physical properties, such as solubility in organic solvents and stability under certain conditions. Its CAS number, 75815-73-5, allows for easy identification in chemical databases, facilitating research and application in fields such as pharmaceuticals, agrochemicals, and materials science. Overall, this compound's distinctive features make it a subject of interest for further study and potential applications.

1-(3-(trifluoromethoxy)phenyl)-1H-pyrazole-4-carbaldehyde

75815-73-5: 1-(3-(Trifluoromethoxy)phenyl)-1H-pyrazole-4-carbaldehyde is a chemical compound characterized by its unique structural features, which include a pyrazole ring and a trifluoromethoxy group. The presence of the trifluoromethoxy substituent enhances its lipophilicity and may influence its reactivity and biological activity. This compound typically exhibits properties associated with aldehydes, such as being a reactive electrophile due to the carbonyl group, which can participate in various chemical reactions, including nucleophilic additions. The pyrazole moiety contributes to its potential as a pharmacophore in medicinal chemistry, as pyrazoles are often found in biologically active compounds. Additionally, the compound may display interesting physical properties, such as solubility in organic solvents and stability under certain conditions. Its CAS number, 75815-73-5, allows for easy identification in chemical databases, facilitating research and application in fields such as pharmaceuticals, agrochemicals, and materials science. Overall, this compound's distinctive features make it a subject of interest for further study and potential applications.

1-[3-(trifluoromethyl)phenyl]-1H-pyrazole-4-carbaldehyde

1-(3-Trifluoromethyl-phenyl)-1H-pyrazole-4-carbaldehyde

CAS 75815-73-5

1-(3-(trifluoromethoxy)phenyl)-1H-pyrazole-4-carbaldehyde

1-[3-(trifluoromethyl)phenyl]-1H-pyrazole-4-carbaldehyde

Ref: IN-DA00G9IA

1-(3-Trifluoromethyl-phenyl)-1H-pyrazole-4-carbaldehyde

Ref: 54-PC104300

1-(3-(trifluoromethyl)phenyl)-1H-pyrazole-4-carbaldehyde

Ref: 3D-ADA81573