Tert-butyl 7-methyl-1H-indole-1-carboxylate 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 compound features a tert-butyl ester group, which enhances its lipophilicity and stability. The presence of the methyl group at the 7-position of the indole ring contributes to its unique chemical properties and potential biological activity. Typically, compounds like this may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The tert-butyl group also serves to protect the carboxylic acid functionality, facilitating further chemical modifications. In terms of solubility, such compounds are generally soluble in organic solvents but may have limited solubility in water due to their hydrophobic characteristics. The compound's reactivity can be influenced by the indole nitrogen, which can participate in various chemical reactions, including electrophilic substitutions. Overall, tert-butyl 7-methyl-1H-indole-1-carboxylate represents a versatile scaffold for further chemical exploration and potential applications in drug development.

tert-butyl 7-methyl-1H-indole-1-carboxylate

442910-62-5: Tert-butyl 7-methyl-1H-indole-1-carboxylate 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 compound features a tert-butyl ester group, which enhances its lipophilicity and stability. The presence of the methyl group at the 7-position of the indole ring contributes to its unique chemical properties and potential biological activity. Typically, compounds like this may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The tert-butyl group also serves to protect the carboxylic acid functionality, facilitating further chemical modifications. In terms of solubility, such compounds are generally soluble in organic solvents but may have limited solubility in water due to their hydrophobic characteristics. The compound's reactivity can be influenced by the indole nitrogen, which can participate in various chemical reactions, including electrophilic substitutions. Overall, tert-butyl 7-methyl-1H-indole-1-carboxylate represents a versatile scaffold for further chemical exploration and potential applications in drug development.

CAS 442910-62-5

tert-butyl 7-methyl-1H-indole-1-carboxylate

1-BOC-7-methylindole

Ref: IN-DA00DACQ

7-Methyl-1H-indole, N-BOC protected

Ref: 54-OR59346

tert-Butyl 7-methyl-1H-indole-1-carboxylate

Ref: 10-F216167