2-Bromo-4-chlorothieno[3,2-c]pyridine is a heterocyclic compound characterized by its unique structure, which includes a thieno ring fused to a pyridine ring, along with bromine and chlorine substituents. This compound typically exhibits a pale yellow to brown appearance and is soluble in organic solvents such as dichloromethane and dimethyl sulfoxide, but may have limited solubility in water. The presence of halogen atoms (bromine and chlorine) contributes to its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and cross-coupling reactions. Its thieno and pyridine moieties can impart interesting biological activities, making it of interest in medicinal chemistry and material science. The compound's molecular structure allows for potential interactions with biological targets, which may lead to applications in pharmaceuticals. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 2-Bromo-4-chlorothieno[3,2-c]pyridine is a versatile compound with significant implications in both synthetic and applied chemistry.

2-Bromo-4-chlorothieno[3,2-c]pyridine

28948-61-0: Thieno[3,2-c]pyridine, 2-bromo-4-chloro-, 2-Bromo-4-chlorothieno[3,2-c]pyridine, 2-Bromo-4-chloro-5-azabenzothiophene

The 2-bromo-4-chlorothieno[3,2-c]pyridine is a pyridine derivative that has been synthesized with the coupling of boronic acid and boronate ester. This fluorescent compound has an emission peak at 489 nm and a quantum yield of 0.14. The substituent on this molecule can be changed to alter the fluorescence properties. This is an example of how quantum chemistry is used in organic synthesis.

CAS 28948-61-0: 2-Bromo-4-chlorothieno[3,2-c]pyridine

2-Bromo-4-chlorothieno[3,2-c]pyridine

Ref: 54-OR59871

2-Bromo-4-chlorothieno[3,2-c]pyridine

Ref: 10-F076775

2-Bromo-4-chlorothieno[3,2-c]pyridine

Ref: 3D-FB151003

Thieno[3,2-c]pyridine, 2-bromo-4-chloro-

Ref: IN-DA002X5Z