6-(Chloroacetyl)-2-benzoxazolinone is a chemical compound characterized by its unique structure, which includes a benzoxazolinone moiety with a chloroacetyl substituent. This compound typically appears as a solid and is known for its potential applications in various fields, including medicinal chemistry and agrochemicals. The presence of the chloroacetyl group contributes to its reactivity, making it a useful intermediate in organic synthesis. It may exhibit biological activity, which can be explored for its potential as a pharmaceutical agent. The compound is soluble in organic solvents, and its reactivity can be influenced by the presence of the chloro group, which can participate in nucleophilic substitution reactions. Safety data indicates that, like many chlorinated compounds, it should be handled with care due to potential toxicity and environmental concerns. Overall, 6-(Chloroacetyl)-2-benzoxazolinone is a versatile compound with significant implications in chemical research and development.

6-(Chloroacetyl)-2-benzoxazolinone

54903-10-5: 2(3H)-Benzoxazolone, 6-(2-chloroacetyl)-, 2(3H)-Benzoxazolone, 6-(chloroacetyl)-, 2-Chloro-1-(2-hydroxy-1,3-benzoxazol-6-yl)ethan-1-one, 6-(2-Chloroacetyl)-2(3H)-benzoxazolone, 6-(Chloroacetyl)-2,3-dihydro-1H-benzoxazol-2-one, 6-(Chloroacetyl)-2,3-dihydrobenzoxazol-2-one, 6-(Chloroacetyl)-2-benzoxazolinone

6-Chloroacetyl-2-benzoxazolinone

6-Chloroacetyl-2-benzoxazolinone is a compound that has been shown to have allelopathic properties. It is used as a herbicide and an insecticide, and it can be used in the treatment of Alzheimer's disease. This active compound inhibits the enzyme acetylcholinesterase, which prevents the breakdown of acetylcholine. 6-Chloroacetyl-2-benzoxazolinone is transported by chloride ions, which are also necessary for its activity. The concentration of this compound can be dose-dependent based on the biomolecular concentration in tissues. 6-Chloroacetyl-2-benzoxazolinone has been shown to inhibit cholinesterase in both apical and basolateral membranes, but it does not penetrate the cell membrane well and is therefore not very effective at inhibiting cholinesterase inside cells. Mutant strains of Escherichia coli have

CAS 54903-10-5: 6-(Chloroacetyl)-2-benzoxazolinone

6-Chloroacetyl-2-benzoxazolinone

Ref: IN-DA003N6A

6-Chloroacetyl-2-benzoxazolinone

Ref: 10-F012240

6-Chloroacetyl-2-benzoxazolinone

Ref: 3D-FC53842