Produktname:2-(Azetidin-3-yl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine

IUPAC Name:3-{5H,6H,7H,8H-imidazo[1,2-a]pyridin-2-yl}azetidine

CAS:2141619-95-4
Molekulare Formel:C10H15N3
Reinheit:95%+
Katalognummer:CM558293
Molekulargewicht:177.25

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Produkt-Details

CAS-Nr.:2141619-95-4
Molekulare Formel:C10H15N3
Schmelzpunkt:-
SMILES-Code:C1(C2=CN3CCCCC3=N2)CNC1
Dichte:
Katalognummer:CM558293
Molekulargewicht:177.25
Siedepunkt:
Mdl-Nr.:
Lagerung:

Category Infos

Imidazoles
Imidazole is an important five-membered nitrogen-containing heterocyclic compound. Among the numerous heterocyclic compounds, imidazole and its derivatives are regarded as a unique and multifaceted scaffold material due to their diverse applications in industrial, organic and pharmaceutical chemistry. Imidazoles interact in different ways with many therapeutic targets, enzymes and receptors in biological systems and thus exhibit a wide range of biological activities. In particular, several imidazoles can be used as clinical drugs to treat various types of cancer with high therapeutic efficacy. Furthermore, imidazoles are one of the most critical segments in the field of anti-covid-19 virus drug discovery due to their ability to interact with active targets in living systems.
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Piperidines
Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.
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Azetidines
Azetidines are an important class of saturated four-membered nitrogen-containing heterocyclic compounds. The research hotspots related to this structure mainly focus on two aspects: one is the research of pharmaceutical chemistry; the other is related to chiral azetidines, using rigid azetidine compounds as chiral ligands for asymmetric catalytic reactions. Many nitrogen-containing heterocycles play important roles in drug structures, and in many cases small structural changes can improve ligand selectivity and pharmacokinetic properties.
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