Methyl 4-(4-(trifluoromethyl)phenoxy)benzoate, identified by the CAS number 1128268-16-5, is an organic compound characterized by its ester functional group, which is formed from the reaction of benzoic acid and methanol. This compound features a trifluoromethyl group, which significantly influences its chemical properties, including increased lipophilicity and potential biological activity. The presence of the phenoxy group enhances its reactivity and solubility in organic solvents. Methyl 4-(4-(trifluoromethyl)phenoxy)benzoate is typically a white to off-white solid at room temperature, with a moderate melting point and boiling point, indicative of its molecular structure. It is often used in various applications, including as an intermediate in organic synthesis and potentially in agrochemical formulations due to its unique electronic properties. Safety data should be consulted for handling, as compounds with trifluoromethyl groups can exhibit toxicity and environmental persistence. Overall, this compound exemplifies the complexity and utility of fluorinated organic molecules in chemical research and industry.

methyl 4-(4-(trifluoromethyl)phenoxy)benzoate(WXC03861)

1128268-16-5: Methyl 4-(4-(trifluoromethyl)phenoxy)benzoate, identified by the CAS number 1128268-16-5, is an organic compound characterized by its ester functional group, which is formed from the reaction of benzoic acid and methanol. This compound features a trifluoromethyl group, which significantly influences its chemical properties, including increased lipophilicity and potential biological activity. The presence of the phenoxy group enhances its reactivity and solubility in organic solvents. Methyl 4-(4-(trifluoromethyl)phenoxy)benzoate is typically a white to off-white solid at room temperature, with a moderate melting point and boiling point, indicative of its molecular structure. It is often used in various applications, including as an intermediate in organic synthesis and potentially in agrochemical formulations due to its unique electronic properties. Safety data should be consulted for handling, as compounds with trifluoromethyl groups can exhibit toxicity and environmental persistence. Overall, this compound exemplifies the complexity and utility of fluorinated organic molecules in chemical research and industry.

CAS 1128268-16-5

methyl 4-(4-(trifluoromethyl)phenoxy)benzoate(WXC03861)

methyl 4-[4-(trifluoromethyl)phenoxy]benzoate

Ref: IN-DA01DJAQ