Methyl 5-(trifluoromethyl)-1H-pyrrole-2-carboxylate is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. The presence of a trifluoromethyl group (-CF3) at the 5-position significantly influences its chemical properties, enhancing its lipophilicity and potentially its reactivity. The carboxylate ester functional group at the 2-position contributes to its ability to participate in various chemical reactions, including nucleophilic substitutions and esterifications. This compound is typically used in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its unique electronic properties and structural versatility. Its trifluoromethyl group can also impart desirable characteristics such as increased metabolic stability and altered biological activity. Safety data sheets should be consulted for handling and storage guidelines, as compounds containing trifluoromethyl groups can exhibit toxicity and environmental persistence. Overall, methyl 5-(trifluoromethyl)-1H-pyrrole-2-carboxylate is a valuable building block in chemical synthesis.

methyl 5-(trifluoromethyl)-1H-pyrrole-2-carboxylate

952182-25-1: Methyl 5-(trifluoromethyl)-1H-pyrrole-2-carboxylate is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. The presence of a trifluoromethyl group (-CF3) at the 5-position significantly influences its chemical properties, enhancing its lipophilicity and potentially its reactivity. The carboxylate ester functional group at the 2-position contributes to its ability to participate in various chemical reactions, including nucleophilic substitutions and esterifications. This compound is typically used in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its unique electronic properties and structural versatility. Its trifluoromethyl group can also impart desirable characteristics such as increased metabolic stability and altered biological activity. Safety data sheets should be consulted for handling and storage guidelines, as compounds containing trifluoromethyl groups can exhibit toxicity and environmental persistence. Overall, methyl 5-(trifluoromethyl)-1H-pyrrole-2-carboxylate is a valuable building block in chemical synthesis.

CAS 952182-25-1

methyl 5-(trifluoromethyl)-1H-pyrrole-2-carboxylate

Methyl 5-(trifluoromethyl)-1H-pyrrole-2-carboxylate

Ref: IN-DA01EEEV

Methyl 5-(trifluoromethyl)-1H-pyrrole-2-carboxylate

Ref: 54-PC48500

Methyl 5-(trifluoromethyl)-1h-pyrrole-2-carboxylate

Ref: 10-F653685