2-Bromo-4,5-di(trifluoromethyl)aniline is an organic compound characterized by the presence of a bromine atom and two trifluoromethyl groups attached to an aniline structure. Its molecular formula reflects the incorporation of bromine and multiple fluorine atoms, which significantly influence its chemical properties. The trifluoromethyl groups are known for their strong electron-withdrawing effects, enhancing the compound's reactivity and stability in various chemical environments. This compound is typically a solid at room temperature and may exhibit low solubility in non-polar solvents due to its polar functional groups. It is often used in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its unique electronic properties and potential for further functionalization. Additionally, the presence of the bromine atom allows for potential substitution reactions, making it a versatile intermediate in chemical synthesis. Safety precautions should be observed when handling this compound, as it may pose health risks due to its halogenated nature.

2-bromo-4,5-di(trifluoromethyl)aniline

230295-15-5: 2-Bromo-4,5-di(trifluoromethyl)aniline is an organic compound characterized by the presence of a bromine atom and two trifluoromethyl groups attached to an aniline structure. Its molecular formula reflects the incorporation of bromine and multiple fluorine atoms, which significantly influence its chemical properties. The trifluoromethyl groups are known for their strong electron-withdrawing effects, enhancing the compound's reactivity and stability in various chemical environments. This compound is typically a solid at room temperature and may exhibit low solubility in non-polar solvents due to its polar functional groups. It is often used in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its unique electronic properties and potential for further functionalization. Additionally, the presence of the bromine atom allows for potential substitution reactions, making it a versatile intermediate in chemical synthesis. Safety precautions should be observed when handling this compound, as it may pose health risks due to its halogenated nature.

CAS 230295-15-5

2-bromo-4,5-di(trifluoromethyl)aniline

Benzenamine, 2-bromo-4,5-bis(trifluoromethyl)-

Ref: IN-DA002LXP

4,5-Bis(trifluoromethyl)-2-bromoaniline

Ref: 54-PC0295

2-Bromo-4,5-di(trifluoromethyl)aniline

Ref: 10-F064677