CAS 107516-75-6: diethyl 1H-indole-2,6-dicarboxylate

Description: 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.

Formula: C₁₄H₁₅NO₄

InChI: InChI=1/C14H15NO4/c1-3-18-13(16)10-6-5-9-7-12(14(17)19-4-2)15-11(9)8-10/h5-8,15H,3-4H2,1-2H3

Diethyl 1H-indole-2,6-dicarboxylate

CAS: 107516-75-6

• Formula: C₁₄H₁₅NO₄
• Purity: 96%
• Color and Shape: Solid
• Molecular weight: 261.2732

Diethyl 1H-indole-2,6-dicarboxylate

CAS: 107516-75-6

• Purity: 95%
• Molecular weight: 261.28g/mol

DIETHYL 1H-INDOLE-2,6-DICARBOXYLATE

CAS: 107516-75-6

• Purity: 97.0%
• Molecular weight: 261.2770080566406

Diethyl indole-2,6-dicarboxylate

CAS: 107516-75-6

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• Formula: C₁₄H₁₅NO₄
• Purity: Min. 95%
• Molecular weight: 261.27 g/mol