5-Trifluoromethyl-6-bromononanaldehyde is a chemical compound characterized by the presence of a trifluoromethyl group and a bromine atom attached to a nonanaldehyde backbone. The trifluoromethyl group is known for its electron-withdrawing properties, which can significantly influence the reactivity and stability of the compound. The aldehyde functional group indicates that it can participate in various chemical reactions, such as nucleophilic addition and oxidation. This compound is likely to be a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. Its unique structure may impart specific properties, such as increased lipophilicity and potential applications in organic synthesis or as an intermediate in the production of pharmaceuticals and agrochemicals. Additionally, the presence of halogens like bromine and fluorine can enhance its biological activity and reactivity, making it of interest in medicinal chemistry. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

5-trifluoromethyl-6-bromoonaldaldehyde

1256836-78-8: 5-Trifluoromethyl-6-bromononanaldehyde is a chemical compound characterized by the presence of a trifluoromethyl group and a bromine atom attached to a nonanaldehyde backbone. The trifluoromethyl group is known for its electron-withdrawing properties, which can significantly influence the reactivity and stability of the compound. The aldehyde functional group indicates that it can participate in various chemical reactions, such as nucleophilic addition and oxidation. This compound is likely to be a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. Its unique structure may impart specific properties, such as increased lipophilicity and potential applications in organic synthesis or as an intermediate in the production of pharmaceuticals and agrochemicals. Additionally, the presence of halogens like bromine and fluorine can enhance its biological activity and reactivity, making it of interest in medicinal chemistry. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

6-Bromo-5-(trifluoromethyl)nicotinaldehyde

CAS 1256836-78-8

5-trifluoromethyl-6-bromoonaldaldehyde

6-Bromo-5-(trifluoromethyl)nicotinaldehyde

Ref: 54-PC1007313