The chemical substance known as (2-bromophenyl)(4-fluorophenyl)methanonato, with the CAS number 573-46-6, is an organic compound characterized by the presence of both bromine and fluorine substituents on aromatic rings. This compound features a methanolate group, which is indicative of its potential reactivity and ability to participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. The bromine atom, being a good leaving group, can facilitate reactions that involve the formation of new carbon-carbon or carbon-heteroatom bonds. The fluorine atom, known for its electronegativity, can influence the electronic properties of the molecule, potentially affecting its reactivity and interaction with other chemical species. The presence of two distinct aromatic rings contributes to the compound's stability and may also impart unique physical properties, such as solubility and melting point. Overall, this compound's structure suggests it could be of interest in fields such as medicinal chemistry or materials science, where halogenated compounds often exhibit valuable biological or physical properties.

(2-bromophenyl)(4-fluorophenyl)methanonato

573-46-6: The chemical substance known as (2-bromophenyl)(4-fluorophenyl)methanonato, with the CAS number 573-46-6, is an organic compound characterized by the presence of both bromine and fluorine substituents on aromatic rings. This compound features a methanolate group, which is indicative of its potential reactivity and ability to participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. The bromine atom, being a good leaving group, can facilitate reactions that involve the formation of new carbon-carbon or carbon-heteroatom bonds. The fluorine atom, known for its electronegativity, can influence the electronic properties of the molecule, potentially affecting its reactivity and interaction with other chemical species. The presence of two distinct aromatic rings contributes to the compound's stability and may also impart unique physical properties, such as solubility and melting point. Overall, this compound's structure suggests it could be of interest in fields such as medicinal chemistry or materials science, where halogenated compounds often exhibit valuable biological or physical properties.

CAS 573-46-6

(2-bromophenyl)(4-fluorophenyl)methanonato

2-Bromo-4'-fluorobenzophenone

Ref: IN-DA00EEUU

(2-Bromophenyl)(4-fluorophenyl)methanone

Ref: 54-PC1002378

2-Bromo-4′-fluorobenzophenone

Ref: 10-F201489