2-Chloro-4-oxoboranyl-benzoyl chloride, identified by its CAS number 850589-38-7, is a chemical compound that features a benzoyl chloride moiety substituted with a boron-containing group. This compound typically exhibits characteristics associated with both aromatic and organoboron chemistry. The presence of the benzoyl chloride functional group suggests that it is reactive, particularly towards nucleophiles, due to the electrophilic nature of the carbonyl carbon. The boron atom in the structure may impart unique reactivity, such as the ability to form complexes with Lewis bases or participate in various coupling reactions. Additionally, the chlorine substituent can influence the compound's reactivity and stability. In terms of physical properties, while specific values may vary, compounds of this nature are often solids or viscous liquids at room temperature and may have moderate solubility in organic solvents. Safety precautions should be taken when handling this compound, as it may be hazardous due to its reactive functional groups. Overall, 2-chloro-4-oxoboranyl-benzoyl chloride is of interest in synthetic organic chemistry and materials science.

2-chloro-4-oxoboranyl-benzoyl chloride

850589-38-7: 2-Chloro-4-oxoboranyl-benzoyl chloride, identified by its CAS number 850589-38-7, is a chemical compound that features a benzoyl chloride moiety substituted with a boron-containing group. This compound typically exhibits characteristics associated with both aromatic and organoboron chemistry. The presence of the benzoyl chloride functional group suggests that it is reactive, particularly towards nucleophiles, due to the electrophilic nature of the carbonyl carbon. The boron atom in the structure may impart unique reactivity, such as the ability to form complexes with Lewis bases or participate in various coupling reactions. Additionally, the chlorine substituent can influence the compound's reactivity and stability. In terms of physical properties, while specific values may vary, compounds of this nature are often solids or viscous liquids at room temperature and may have moderate solubility in organic solvents. Safety precautions should be taken when handling this compound, as it may be hazardous due to its reactive functional groups. Overall, 2-chloro-4-oxoboranyl-benzoyl chloride is of interest in synthetic organic chemistry and materials science.

CAS 850589-38-7

2-chloro-4-oxoboranyl-benzoyl chloride

3-Chloro-4-chlorocarbonylphenylboronic anhydride

Ref: IN-DA003BRT

3-Chloro-4-(chlorocarbonyl)benzeneboronic anhydride

Ref: 54-OR4219