Ethyl (4-chloro-2-nitrophenoxy)acetate is an organic compound characterized by its ester functional group, which is formed from the reaction of ethyl alcohol and a substituted phenolic compound. This substance features a chloro group and a nitro group on the aromatic ring, contributing to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of the nitro group typically enhances the compound's electrophilic character, while the chloro group can influence its solubility and stability. Ethyl (4-chloro-2-nitrophenoxy)acetate is likely to be a pale yellow to light brown liquid or solid, depending on its purity and form. It is important to handle this compound with care, as it may pose health risks, including toxicity and environmental hazards. Proper safety measures should be observed when working with this chemical, including the use of personal protective equipment and adherence to relevant regulations. Its specific applications and reactivity can be further explored in the context of synthetic organic chemistry.

ethyl (4-chloro-2-nitrophenoxy)acetate

108274-38-0: Ethyl (4-chloro-2-nitrophenoxy)acetate is an organic compound characterized by its ester functional group, which is formed from the reaction of ethyl alcohol and a substituted phenolic compound. This substance features a chloro group and a nitro group on the aromatic ring, contributing to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of the nitro group typically enhances the compound's electrophilic character, while the chloro group can influence its solubility and stability. Ethyl (4-chloro-2-nitrophenoxy)acetate is likely to be a pale yellow to light brown liquid or solid, depending on its purity and form. It is important to handle this compound with care, as it may pose health risks, including toxicity and environmental hazards. Proper safety measures should be observed when working with this chemical, including the use of personal protective equipment and adherence to relevant regulations. Its specific applications and reactivity can be further explored in the context of synthetic organic chemistry.

CAS 108274-38-0

ethyl (4-chloro-2-nitrophenoxy)acetate

Ethyl 2-(4-Chloro-2-nitrophenyl)acetate

Ref: IN-DA003Q1M

ETHYL 2-(4-CHLORO-2-NITROPHENYL)ACETATE

Ref: 10-F536200