3-Amino-5-chloro-6-methyl-7-azaindole is a heterocyclic compound that belongs to the class of azaindoles, which are derivatives of indole containing nitrogen atoms in the ring structure. This compound features an amino group, a chlorine atom, and a methyl group, contributing to its unique chemical properties. The presence of the amino group typically imparts basic characteristics, allowing it to participate in various chemical reactions, such as nucleophilic substitutions. The chlorine atom introduces electronegativity, which can influence the compound's reactivity and solubility in different solvents. The methyl group can affect the steric hindrance and overall stability of the molecule. 3-Amino-5-chloro-6-methyl-7-azaindole may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of new drugs. Its structural features suggest potential applications in medicinal chemistry, where modifications to the azaindole framework can lead to compounds with enhanced efficacy or selectivity for specific biological targets.

3-AMINO-5-CHLORO-6-METHYL-7-AZAINDOLE

1000340-14-6: 3-Amino-5-chloro-6-methyl-7-azaindole is a heterocyclic compound that belongs to the class of azaindoles, which are derivatives of indole containing nitrogen atoms in the ring structure. This compound features an amino group, a chlorine atom, and a methyl group, contributing to its unique chemical properties. The presence of the amino group typically imparts basic characteristics, allowing it to participate in various chemical reactions, such as nucleophilic substitutions. The chlorine atom introduces electronegativity, which can influence the compound's reactivity and solubility in different solvents. The methyl group can affect the steric hindrance and overall stability of the molecule. 3-Amino-5-chloro-6-methyl-7-azaindole may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of new drugs. Its structural features suggest potential applications in medicinal chemistry, where modifications to the azaindole framework can lead to compounds with enhanced efficacy or selectivity for specific biological targets.

CAS 1000340-14-6

3-AMINO-5-CHLORO-6-METHYL-7-AZAINDOLE

5-Chloro-6-methyl-1H-pyrrolo[2,3-b]pyridin-3-amine

Ref: IN-DA0000D6