2-Bromo-5-chloro-[1,2,4]triazolo[1,5-a]pyridine is a heterocyclic compound characterized by its unique triazole and pyridine ring structures. This compound features a bromine atom and a chlorine atom as substituents, which can influence its reactivity and biological activity. The presence of the triazole ring contributes to its potential as a pharmacophore in medicinal chemistry, often associated with various biological activities, including antimicrobial and antifungal properties. The chlorine and bromine substituents can enhance lipophilicity and affect the compound's interaction with biological targets. Additionally, the compound's structure suggests it may participate in hydrogen bonding and other intermolecular interactions, which are critical for its function in biological systems. Its synthesis typically involves multi-step organic reactions, and it may be used in research settings to explore its potential applications in drug development or as a chemical probe in biological studies. As with many halogenated compounds, considerations regarding environmental impact and safety are essential during handling and disposal.

2-BroMo-5-chloro-[1,2,4]triazolo[1,5-a]pyridine

1784176-14-2: 2-Bromo-5-chloro-[1,2,4]triazolo[1,5-a]pyridine is a heterocyclic compound characterized by its unique triazole and pyridine ring structures. This compound features a bromine atom and a chlorine atom as substituents, which can influence its reactivity and biological activity. The presence of the triazole ring contributes to its potential as a pharmacophore in medicinal chemistry, often associated with various biological activities, including antimicrobial and antifungal properties. The chlorine and bromine substituents can enhance lipophilicity and affect the compound's interaction with biological targets. Additionally, the compound's structure suggests it may participate in hydrogen bonding and other intermolecular interactions, which are critical for its function in biological systems. Its synthesis typically involves multi-step organic reactions, and it may be used in research settings to explore its potential applications in drug development or as a chemical probe in biological studies. As with many halogenated compounds, considerations regarding environmental impact and safety are essential during handling and disposal.

2-Bromo-5-chloro-[1,2,4]triazolo[1,5-a]pyridine

<p>2-Bromo-5-chloro-[1,2,4]triazolo[1,5-a]pyridine</p>

CAS 1784176-14-2

2-BroMo-5-chloro-[1,2,4]triazolo[1,5-a]pyridine

2-Bromo-5-chloro-[1,2,4]triazolo[1,5-a]pyridine

Ref: IN-DA00HZTY

2-Bromo-5-chloro-[1,2,4]triazolo[1,5-a]pyridine

Ref: 54-OR1032497

2-Bromo-5-chloro-[1,2,4]triazolo[1,5-a]pyridine

Ref: 10-F869973