2-Amino-6-chloro-3-formylchromone is a chemical compound belonging to the chromone family, characterized by a chromone backbone with specific functional groups. It features an amino group (-NH2) and a formyl group (-CHO) at the 3 and 6 positions, respectively, along with a chlorine atom at the 6 position of the chromone ring. This compound exhibits properties typical of chromones, such as potential biological activity, including antimicrobial and anti-inflammatory effects. The presence of the amino and formyl groups can enhance its reactivity and solubility in various solvents, making it useful in organic synthesis and medicinal chemistry. Additionally, the chlorine substituent may influence its electronic properties and reactivity, potentially allowing for further derivatization. The compound's structure suggests it may participate in various chemical reactions, including nucleophilic substitutions and condensation reactions, which are common in the synthesis of more complex organic molecules. Overall, 2-amino-6-chloro-3-formylchromone is of interest for its potential applications in pharmaceuticals and materials science.

2-amino-6-chloro-3-formylchromone

68301-77-9: 2-Amino-6-chloro-3-formylchromone is a chemical compound belonging to the chromone family, characterized by a chromone backbone with specific functional groups. It features an amino group (-NH2) and a formyl group (-CHO) at the 3 and 6 positions, respectively, along with a chlorine atom at the 6 position of the chromone ring. This compound exhibits properties typical of chromones, such as potential biological activity, including antimicrobial and anti-inflammatory effects. The presence of the amino and formyl groups can enhance its reactivity and solubility in various solvents, making it useful in organic synthesis and medicinal chemistry. Additionally, the chlorine substituent may influence its electronic properties and reactivity, potentially allowing for further derivatization. The compound's structure suggests it may participate in various chemical reactions, including nucleophilic substitutions and condensation reactions, which are common in the synthesis of more complex organic molecules. Overall, 2-amino-6-chloro-3-formylchromone is of interest for its potential applications in pharmaceuticals and materials science.

CAS 68301-77-9

2-amino-6-chloro-3-formylchromone

2-Amino-6-chloro-3-formylchromone

Ref: 3B-A2743

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