3-Bromoimidazo[1,2-a]pyridin-6-amine is a heterocyclic organic compound characterized by the presence of both bromine and an imidazo-pyridine structure. This compound features a fused ring system that includes an imidazole and a pyridine moiety, contributing to its potential biological activity. The bromine atom is located at the 3-position of the imidazole ring, which can influence the compound's reactivity and interactions with biological targets. The amino group at the 6-position of the pyridine ring enhances its solubility and can participate in hydrogen bonding, making it a candidate for various chemical reactions and applications in medicinal chemistry. Compounds of this type are often investigated for their pharmacological properties, including antimicrobial and anticancer activities. Additionally, the presence of halogens like bromine can affect the compound's electronic properties, potentially enhancing its reactivity in substitution reactions. Overall, 3-bromoimidazo[1,2-a]pyridin-6-amine is of interest in the field of drug discovery and development due to its unique structural features and potential biological applications.

3-bromoimidazo[1,2-a]pyridin-6-amine

1099621-14-3: 3-Bromoimidazo[1,2-a]pyridin-6-amine is a heterocyclic organic compound characterized by the presence of both bromine and an imidazo-pyridine structure. This compound features a fused ring system that includes an imidazole and a pyridine moiety, contributing to its potential biological activity. The bromine atom is located at the 3-position of the imidazole ring, which can influence the compound's reactivity and interactions with biological targets. The amino group at the 6-position of the pyridine ring enhances its solubility and can participate in hydrogen bonding, making it a candidate for various chemical reactions and applications in medicinal chemistry. Compounds of this type are often investigated for their pharmacological properties, including antimicrobial and anticancer activities. Additionally, the presence of halogens like bromine can affect the compound's electronic properties, potentially enhancing its reactivity in substitution reactions. Overall, 3-bromoimidazo[1,2-a]pyridin-6-amine is of interest in the field of drug discovery and development due to its unique structural features and potential biological applications.

<p>3-Bromoimidazo[1,2-a]pyridin-6-amine</p>

CAS 1099621-14-3

3-bromoimidazo[1,2-a]pyridin-6-amine

3-bromoimidazo[1,2-a]pyridin-6-amine

Ref: IN-DA003N2I

3-Bromoimidazo[1,2-a]pyridin-6-amine

Ref: 54-OR1021469

3-Bromoimidazo[1,2-a]pyridin-6-amine

Ref: 10-F320408