1H-Indol-6-ol, 5-methoxy-, acetate (ester), with the CAS number 112919-69-4, is a chemical compound that belongs to the indole family, which is characterized by a bicyclic structure containing a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. This specific compound features a methoxy group at the 5-position and an acetate group at the 6-position of the indole structure, which can influence its solubility, reactivity, and biological activity. The presence of the methoxy group typically enhances lipophilicity, potentially affecting the compound's interaction with biological membranes. As an ester, it may undergo hydrolysis in the presence of water or enzymes, releasing the corresponding alcohol and acetic acid. Compounds of this nature are often studied for their pharmacological properties, including potential anti-inflammatory, antimicrobial, or anticancer activities, due to the diverse biological roles of indole derivatives. However, specific applications and effects would depend on further empirical studies and context within medicinal chemistry.

1H-Indol-6-ol, 5-methoxy-, acetate (ester)

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5-Acetoxy-6-methoxyindole is a fine chemical, useful building block, and research chemical with CAS No. 112919-69-4. It is a versatile building block and reaction component that can be used as a reagent or speciality chemical in the synthesis of other complex compounds. 5-Acetoxy-6-methoxyindole is also used as an intermediate in the synthesis of drugs and pharmaceuticals. This compound has high purity, making it a high quality product with many uses.

CAS 112919-69-4: 1H-Indol-6-ol, 5-methoxy-, acetate (ester)

5-Acetoxy-6-methoxyindole

Ref: 3D-FA66170