5-Nitro-2-(piperidin-3-yloxy)-pyridinehydrochloride

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Reagent Code: #219598
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CAS Number 1185312-46-2

science Other reagents with same CAS 1185312-46-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.689 g/mol
Formula C₁₀H₁₄ClN₃O₃
badge Registry Numbers
MDL Number MFCD09607580
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as a key intermediate in the synthesis of varenicline, a medication for smoking cessation. It plays a critical role in constructing the core structure of varenicline due to its functional groups, which allow for selective chemical transformations. The nitro group enables reduction to an amine, facilitating further coupling reactions, while the piperidinyl-oxygen linkage contributes to the molecule’s affinity for nicotinic acetylcholine receptors. Its hydrochloride salt form enhances stability and solubility, making it suitable for use in pharmaceutical manufacturing processes.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿29,360.00

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5-Nitro-2-(piperidin-3-yloxy)-pyridinehydrochloride
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Used primarily as a key intermediate in the synthesis of varenicline, a medication for smoking cessation. It plays a critical role in constructing the core structure of varenicline due to its functional groups, which allow for selective chemical transformations. The nitro group enables reduction to an amine, facilitating further coupling reactions, while the piperidinyl-oxygen linkage contributes to the molecule’s affinity for nicotinic acetylcholine receptors. Its hydrochloride salt form enhances stabil

Used primarily as a key intermediate in the synthesis of varenicline, a medication for smoking cessation. It plays a critical role in constructing the core structure of varenicline due to its functional groups, which allow for selective chemical transformations. The nitro group enables reduction to an amine, facilitating further coupling reactions, while the piperidinyl-oxygen linkage contributes to the molecule’s affinity for nicotinic acetylcholine receptors. Its hydrochloride salt form enhances stability and solubility, making it suitable for use in pharmaceutical manufacturing processes.

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