4'-Chlorobiphenyl-3-carbaldehyde, with the CAS number 139502-80-0, is an organic compound characterized by its biphenyl structure, which consists of two phenyl rings connected by a single bond. The presence of a chlorinated substituent at the para position of one phenyl ring and an aldehyde functional group at the meta position of the other ring defines its chemical properties. This compound is typically a solid at room temperature and exhibits moderate solubility in organic solvents due to its hydrophobic nature. It may participate in various chemical reactions, including nucleophilic additions and electrophilic substitutions, owing to the reactivity of the aldehyde group. Additionally, the chlorinated biphenyl structure can influence its electronic properties and stability, making it of interest in fields such as organic synthesis and materials science. Safety data should be consulted, as chlorinated compounds can exhibit toxicity and environmental persistence. Overall, 4'-chlorobiphenyl-3-carbaldehyde serves as a valuable intermediate in the synthesis of more complex organic molecules.

4'-CHLOROBIPHENYL-3-CARBALDEHYDE

139502-80-0: 4'-Chlorobiphenyl-3-carbaldehyde, with the CAS number 139502-80-0, is an organic compound characterized by its biphenyl structure, which consists of two phenyl rings connected by a single bond. The presence of a chlorinated substituent at the para position of one phenyl ring and an aldehyde functional group at the meta position of the other ring defines its chemical properties. This compound is typically a solid at room temperature and exhibits moderate solubility in organic solvents due to its hydrophobic nature. It may participate in various chemical reactions, including nucleophilic additions and electrophilic substitutions, owing to the reactivity of the aldehyde group. Additionally, the chlorinated biphenyl structure can influence its electronic properties and stability, making it of interest in fields such as organic synthesis and materials science. Safety data should be consulted, as chlorinated compounds can exhibit toxicity and environmental persistence. Overall, 4'-chlorobiphenyl-3-carbaldehyde serves as a valuable intermediate in the synthesis of more complex organic molecules.

[1,1'-Biphenyl]-3-carboxaldehyde, 4'-chloro-

4'-Chloro-[1,1'-biphenyl]-3-carboxaldehyde

CAS 139502-80-0

4'-CHLOROBIPHENYL-3-CARBALDEHYDE

[1,1'-Biphenyl]-3-carboxaldehyde, 4'-chloro-

Ref: IN-DA001B5A

4'-Chloro-[1,1'-biphenyl]-3-carboxaldehyde

Ref: 54-OR7356

4′-Chlorobiphenyl-3-carbaldehyde

Ref: 10-F014282