Tert-butyl 3-bromo-7-methyl-indole-1-carboxylate is a chemical 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 a bromine atom at the 3-position and a methyl group at the 7-position of the indole ring contributes to its unique reactivity and potential biological activity. The tert-butyl group also serves to protect the carboxylic acid functionality, making it useful in various synthetic applications. This compound may be utilized in medicinal chemistry for the development of pharmaceuticals, particularly due to the indole moiety's prevalence in biologically active compounds. Its properties, such as solubility, melting point, and reactivity, can vary based on the specific conditions and solvents used in experiments. As with many organic compounds, handling should be done with care, considering safety protocols to mitigate any potential hazards associated with its use.

tert-butyl 3-bromo-7-methyl-indole-1-carboxylate

914349-39-6: Tert-butyl 3-bromo-7-methyl-indole-1-carboxylate is a chemical 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 a bromine atom at the 3-position and a methyl group at the 7-position of the indole ring contributes to its unique reactivity and potential biological activity. The tert-butyl group also serves to protect the carboxylic acid functionality, making it useful in various synthetic applications. This compound may be utilized in medicinal chemistry for the development of pharmaceuticals, particularly due to the indole moiety's prevalence in biologically active compounds. Its properties, such as solubility, melting point, and reactivity, can vary based on the specific conditions and solvents used in experiments. As with many organic compounds, handling should be done with care, considering safety protocols to mitigate any potential hazards associated with its use.

3-Bromo-7-methylindole-1-carboxylic acid tert-butyl ester

3-Bromo-7-methyl-1H-indole, N-BOC protected

CAS 914349-39-6

tert-butyl 3-bromo-7-methyl-indole-1-carboxylate

3-Bromo-7-methylindole-1-carboxylic acid tert-butyl ester

Ref: IN-DA00H02Q

3-Bromo-7-methyl-1H-indole, N-BOC protected

Ref: 54-OR1741