Pyrazolo[1,5-a]pyridine-3-carbonyl chloride is a heterocyclic organic compound characterized by its unique bicyclic structure, which consists of a pyrazole ring fused to a pyridine ring. This compound features a carbonyl chloride functional group, making it a reactive acyl chloride derivative. It is typically used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in various chemical reactions, such as acylation and nucleophilic substitutions. The presence of the carbonyl chloride group enhances its reactivity, allowing for the introduction of diverse functional groups. Pyrazolo[1,5-a]pyridine derivatives are of interest in medicinal chemistry for their potential biological activities, including anti-inflammatory and anti-cancer properties. The compound is generally handled with care due to its reactivity and potential hazards associated with the carbonyl chloride moiety, which can release hydrochloric acid upon hydrolysis. Proper safety measures should be observed when working with this substance in a laboratory setting.

pyrazolo[1,5-a]pyridine-3-carbonyl chloride

78933-24-1: Pyrazolo[1,5-a]pyridine-3-carbonyl chloride is a heterocyclic organic compound characterized by its unique bicyclic structure, which consists of a pyrazole ring fused to a pyridine ring. This compound features a carbonyl chloride functional group, making it a reactive acyl chloride derivative. It is typically used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in various chemical reactions, such as acylation and nucleophilic substitutions. The presence of the carbonyl chloride group enhances its reactivity, allowing for the introduction of diverse functional groups. Pyrazolo[1,5-a]pyridine derivatives are of interest in medicinal chemistry for their potential biological activities, including anti-inflammatory and anti-cancer properties. The compound is generally handled with care due to its reactivity and potential hazards associated with the carbonyl chloride moiety, which can release hydrochloric acid upon hydrolysis. Proper safety measures should be observed when working with this substance in a laboratory setting.

Pyrazolo[1,5-a]pyridine-3-carbonyl chloride

CAS 78933-24-1

pyrazolo[1,5-a]pyridine-3-carbonyl chloride

Pyrazolo[1,5-a]pyridine-3-carbonyl chloride

Ref: 54-OR14302