(3-Bromophenyl)propanedial, with the CAS number 791809-62-6, is an organic compound characterized by the presence of a bromine atom attached to a phenyl group, which is further connected to a propanedial moiety. This compound features two aldehyde functional groups (-CHO) at the terminal ends of a three-carbon chain, contributing to its reactivity and potential applications in organic synthesis. The bromine substituent enhances the electrophilic character of the aromatic ring, making it a useful intermediate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The presence of the aldehyde groups allows for further functionalization, enabling the synthesis of more complex molecules. Additionally, (3-bromophenyl)propanedial may exhibit specific physical properties such as solubility in organic solvents and distinct melting and boiling points, which are typical for compounds with similar structures. Its unique combination of functional groups makes it a valuable compound in medicinal chemistry and materials science, where it can serve as a building block for more complex organic compounds.

(3-bromophenyl)propanedial

791809-62-6: (3-Bromophenyl)propanedial, with the CAS number 791809-62-6, is an organic compound characterized by the presence of a bromine atom attached to a phenyl group, which is further connected to a propanedial moiety. This compound features two aldehyde functional groups (-CHO) at the terminal ends of a three-carbon chain, contributing to its reactivity and potential applications in organic synthesis. The bromine substituent enhances the electrophilic character of the aromatic ring, making it a useful intermediate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The presence of the aldehyde groups allows for further functionalization, enabling the synthesis of more complex molecules. Additionally, (3-bromophenyl)propanedial may exhibit specific physical properties such as solubility in organic solvents and distinct melting and boiling points, which are typical for compounds with similar structures. Its unique combination of functional groups makes it a valuable compound in medicinal chemistry and materials science, where it can serve as a building block for more complex organic compounds.

CAS 791809-62-6

(3-bromophenyl)propanedial

2-(3-Bromophenyl)malondialdehyde

Ref: 54-OR7620

2-(3-Bromophenyl)malondialdehyde

Ref: 10-F023525

2-(3-Bromophenyl)malondialdehyde

Ref: 3D-RGB80962