4-[(3-Bromobenzyl)oxy]benzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group and a bromobenzyl ether moiety. The presence of the bromine atom introduces both electronegative character and potential for further chemical reactivity, making it a valuable intermediate in organic synthesis. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents such as ethanol and dichloromethane, but may have limited solubility in water due to its hydrophobic aromatic components. Its molecular structure allows for various applications in pharmaceuticals, agrochemicals, and materials science, particularly in the synthesis of more complex molecules. The compound's reactivity can be influenced by the bromine substituent, which can participate in nucleophilic substitution reactions. Additionally, the aldehyde group can undergo oxidation or condensation reactions, making it a versatile building block in synthetic organic chemistry. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken.

4-[(3-bromobenzyl)oxy]benzaldehyde

588676-02-2: 4-[(3-Bromobenzyl)oxy]benzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group and a bromobenzyl ether moiety. The presence of the bromine atom introduces both electronegative character and potential for further chemical reactivity, making it a valuable intermediate in organic synthesis. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents such as ethanol and dichloromethane, but may have limited solubility in water due to its hydrophobic aromatic components. Its molecular structure allows for various applications in pharmaceuticals, agrochemicals, and materials science, particularly in the synthesis of more complex molecules. The compound's reactivity can be influenced by the bromine substituent, which can participate in nucleophilic substitution reactions. Additionally, the aldehyde group can undergo oxidation or condensation reactions, making it a versatile building block in synthetic organic chemistry. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken.

CAS 588676-02-2

4-[(3-bromobenzyl)oxy]benzaldehyde

4-[(3-bromobenzyl)oxy]benzaldehyde

Ref: IN-DA00EA5C