5-Bromo-2,3,4-trifluorobenzaldehyde is an aromatic aldehyde characterized by the presence of a bromine atom and three fluorine atoms substituted on a benzene ring. The molecular structure features a benzaldehyde functional group, which is indicative of its reactivity and potential applications in organic synthesis. The presence of the bromine and trifluoromethyl groups significantly influences its electronic properties, making it a useful compound in various chemical reactions, including electrophilic aromatic substitution and cross-coupling reactions. This compound is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. Its unique combination of halogen substituents can enhance its lipophilicity and alter its boiling and melting points compared to non-substituted benzaldehydes. Additionally, 5-bromo-2,3,4-trifluorobenzaldehyde may exhibit interesting biological activities, making it a candidate for further research in medicinal chemistry. Safety precautions should be taken when handling this compound, as halogenated compounds can pose health risks.

5-bromo-2,3,4-trifluorobenzaldehyde

914935-69-6: 5-Bromo-2,3,4-trifluorobenzaldehyde is an aromatic aldehyde characterized by the presence of a bromine atom and three fluorine atoms substituted on a benzene ring. The molecular structure features a benzaldehyde functional group, which is indicative of its reactivity and potential applications in organic synthesis. The presence of the bromine and trifluoromethyl groups significantly influences its electronic properties, making it a useful compound in various chemical reactions, including electrophilic aromatic substitution and cross-coupling reactions. This compound is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. Its unique combination of halogen substituents can enhance its lipophilicity and alter its boiling and melting points compared to non-substituted benzaldehydes. Additionally, 5-bromo-2,3,4-trifluorobenzaldehyde may exhibit interesting biological activities, making it a candidate for further research in medicinal chemistry. Safety precautions should be taken when handling this compound, as halogenated compounds can pose health risks.

5-Bromo-2,3,4-trifluorobenzaldehyde

<p>5-Bromo-2,3,4-trifluorobenzaldehyde</p>

CAS 914935-69-6

5-bromo-2,3,4-trifluorobenzaldehyde

5-Bromo-2,3,4-trifluorobenzaldehyde

Ref: IN-DA01K8S9

5-Bromo-2,3,4-trifluorobenzaldehyde

Ref: 54-PC57777

5-Bromo-2,3,4-trifluorobenzaldehyde

Ref: 10-F629616