Tert-butyl 4-(bromomethyl)-4-methylpiperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. This compound features a tert-butyl ester group, contributing to its lipophilicity and potential applications in organic synthesis and medicinal chemistry. The presence of a bromomethyl group indicates that it can participate in nucleophilic substitution reactions, making it a versatile intermediate in the synthesis of more complex molecules. The methyl group on the piperidine ring adds to the steric bulk, which can influence the compound's reactivity and interaction with biological targets. Additionally, the carboxylate functional group suggests potential for forming salts or participating in esterification reactions. Overall, this compound's unique structure and functional groups make it of interest in various chemical applications, particularly in the development of pharmaceuticals or agrochemicals. As with any chemical substance, proper handling and safety precautions should be observed due to its reactivity and potential hazards associated with brominated compounds.

tert-butyl 4-(bromomethyl)-4-methylpiperidine-1-carboxylate

1363383-33-8: Tert-butyl 4-(bromomethyl)-4-methylpiperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. This compound features a tert-butyl ester group, contributing to its lipophilicity and potential applications in organic synthesis and medicinal chemistry. The presence of a bromomethyl group indicates that it can participate in nucleophilic substitution reactions, making it a versatile intermediate in the synthesis of more complex molecules. The methyl group on the piperidine ring adds to the steric bulk, which can influence the compound's reactivity and interaction with biological targets. Additionally, the carboxylate functional group suggests potential for forming salts or participating in esterification reactions. Overall, this compound's unique structure and functional groups make it of interest in various chemical applications, particularly in the development of pharmaceuticals or agrochemicals. As with any chemical substance, proper handling and safety precautions should be observed due to its reactivity and potential hazards associated with brominated compounds.

1-Piperidinecarboxylic acid, 4-(bromomethyl)-4-methyl-, 1,1-dimethylethyl ester

<p>4-Bromomethyl-1-Boc-4-methylpiperidine</p>

CAS 1363383-33-8

tert-butyl 4-(bromomethyl)-4-methylpiperidine-1-carboxylate

1-Piperidinecarboxylic acid, 4-(bromomethyl)-4-methyl-, 1,1-dimethylethyl ester

Ref: IN-DA0011RJ

4-Bromomethyl-1-Boc-4-methylpiperidine

Ref: 54-OR1021668

4-BROMOMETHYL-1-BOC-4-METHYLPIPERIDINE

Ref: 10-F468012