Tert-butyl 3-(hydroxymethyl)-5-methoxy-1H-indole-1-carboxylate, with the CAS number 600136-09-2, is a chemical compound that belongs to the indole family, characterized by its indole core structure. This compound features a tert-butyl ester group, which enhances its lipophilicity and stability, making it suitable for various applications in organic synthesis and medicinal chemistry. The presence of a hydroxymethyl group and a methoxy group on the indole ring contributes to its potential biological activity, possibly influencing its interactions with biological targets. The compound is typically synthesized through multi-step organic reactions, which may involve protecting group strategies due to the presence of multiple functional groups. Its solubility properties are influenced by the tert-butyl and methoxy groups, allowing for potential use in drug formulation. As with many indole derivatives, it may exhibit interesting pharmacological properties, warranting further investigation into its biological effects and therapeutic potential. Safety and handling precautions should be observed, as with all chemical substances, due to potential hazards associated with its use.

tert-butyl 3-(hydroxymethyl)-5-methoxy-1H-indole-1-carboxylate

600136-09-2: Tert-butyl 3-(hydroxymethyl)-5-methoxy-1H-indole-1-carboxylate, with the CAS number 600136-09-2, is a chemical compound that belongs to the indole family, characterized by its indole core structure. This compound features a tert-butyl ester group, which enhances its lipophilicity and stability, making it suitable for various applications in organic synthesis and medicinal chemistry. The presence of a hydroxymethyl group and a methoxy group on the indole ring contributes to its potential biological activity, possibly influencing its interactions with biological targets. The compound is typically synthesized through multi-step organic reactions, which may involve protecting group strategies due to the presence of multiple functional groups. Its solubility properties are influenced by the tert-butyl and methoxy groups, allowing for potential use in drug formulation. As with many indole derivatives, it may exhibit interesting pharmacological properties, warranting further investigation into its biological effects and therapeutic potential. Safety and handling precautions should be observed, as with all chemical substances, due to potential hazards associated with its use.

CAS 600136-09-2

tert-butyl 3-(hydroxymethyl)-5-methoxy-1H-indole-1-carboxylate

3-Hydroxymethyl-5-methoxyindole-1-carboxylic acid tert-butyl ester

Ref: IN-DA00E9V6

3-(Hydroxymethyl)-5-methoxy-1H-indole, N-BOC protected

Ref: 54-OR1699