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Structure of 206446-45-9
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This pyridine derivative features a sterically constrained azetidinyl group, delivering enhanced metabolic stability and improved membrane permeability. The dihydrochloride salt form ensures excellent solubility and crystalline handling under standard conditions. Designed for medicinal chemistry applications, it integrates efficiently into targeted molecular scaffolds requiring nitrogen-rich heterocyclic motifs.
2-(Azetidin-3-yl)pyridinedihydrochloride serves as a versatile building block in medicinal chemistry, enabling efficient construction of nitrogen-containing heterocycles. Its azetidine moiety offers enhanced metabolic stability and improved solubility profiles, while the pyridine ring facilitates diverse functionalization via electrophilic substitution or transition-metal-catalyzed coupling. The dihydrochloride salt form enhances crystallinity and handling stability, simplifying purification and storage—ideal for high-throughput synthesis and API development workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: