Diethyl 1H-indole-2,6-dicarboxylate is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This substance features two ester functional groups derived from diethyl esterification of the dicarboxylic acid at the 2 and 6 positions of the indole ring. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The compound is known for its potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to the reactivity of its ester groups. It may exhibit biological activity, making it of interest in medicinal chemistry. As with many organic compounds, it is important to handle diethyl 1H-indole-2,6-dicarboxylate with care, following appropriate safety protocols to mitigate risks associated with chemical exposure. Its solubility in organic solvents and stability under standard laboratory conditions are also notable characteristics that facilitate its use in various chemical reactions.

diethyl 1H-indole-2,6-dicarboxylate

107516-75-6: Diethyl 1H-indole-2,6-dicarboxylate is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This substance features two ester functional groups derived from diethyl esterification of the dicarboxylic acid at the 2 and 6 positions of the indole ring. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The compound is known for its potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to the reactivity of its ester groups. It may exhibit biological activity, making it of interest in medicinal chemistry. As with many organic compounds, it is important to handle diethyl 1H-indole-2,6-dicarboxylate with care, following appropriate safety protocols to mitigate risks associated with chemical exposure. Its solubility in organic solvents and stability under standard laboratory conditions are also notable characteristics that facilitate its use in various chemical reactions.

CAS 107516-75-6

diethyl 1H-indole-2,6-dicarboxylate

DIETHYL 1H-INDOLE-2,6-DICARBOXYLATE

Ref: IN-DA003PF5

Diethyl 1H-indole-2,6-dicarboxylate

Ref: 54-OR91438

DIETHYL 1H-INDOLE-2,6-DICARBOXYLATE

Ref: 10-F301909