5-Bromo-2-methylbenzaldehyde is an organic compound characterized by its aromatic structure, which includes a bromine atom and a methyl group attached to a benzaldehyde moiety. This compound features a bromine substituent at the 5-position and a methyl group at the 2-position of the benzene ring, contributing to its unique reactivity and properties. It is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of the aldehyde functional group (-CHO) makes it a reactive species, capable of participating in various chemical reactions, such as nucleophilic additions and condensation reactions. Additionally, the bromine atom can serve as a site for further substitution reactions, enhancing its utility in organic synthesis. 5-Bromo-2-methylbenzaldehyde is used in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals, owing to its versatile reactivity and the ability to introduce functional groups into complex molecular architectures. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested.

5-Bromo-2-methylbenzaldehyde

90050-59-2: 5-Bromo-2-methylbenzaldehyde is an organic compound characterized by its aromatic structure, which includes a bromine atom and a methyl group attached to a benzaldehyde moiety. This compound features a bromine substituent at the 5-position and a methyl group at the 2-position of the benzene ring, contributing to its unique reactivity and properties. It is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of the aldehyde functional group (-CHO) makes it a reactive species, capable of participating in various chemical reactions, such as nucleophilic additions and condensation reactions. Additionally, the bromine atom can serve as a site for further substitution reactions, enhancing its utility in organic synthesis. 5-Bromo-2-methylbenzaldehyde is used in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals, owing to its versatile reactivity and the ability to introduce functional groups into complex molecular architectures. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested.

CAS 90050-59-2

5-Bromo-2-methylbenzaldehyde

5-Bromo-2-methylbenzaldehyde

Ref: 3B-B5036

Benzaldehyde, 5-bromo-2-methyl-

Ref: IN-DA00IFZM

5-Bromo-2-methylbenzaldehyde

Ref: 54-OR909370

5-Bromo-2-methylbenzaldehyde

Ref: 10-F047056