3-Nitro-2-(piperidin-3-ylmethoxy)-pyridinehydrochloride

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Reagent Code: #219593
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CAS Number 1185310-12-6

science Other reagents with same CAS 1185310-12-6

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scatter_plot Molecular Information
Weight 273.72 g/mol
Formula C₁₁H₁₆ClN₃O₃
badge Registry Numbers
MDL Number MFCD09877663
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to engage in hydrogen bonding and π-π interactions, enhancing binding affinity to target proteins. Commonly employed in the preparation of small molecule drugs targeting neurological disorders and inflammatory diseases. Its nitro and piperidine functionalities allow for further chemical modifications, enabling the optimization of pharmacokinetic properties such as solubility and metabolic stability.

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

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3-Nitro-2-(piperidin-3-ylmethoxy)-pyridinehydrochloride
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to engage in hydrogen bonding and π-π interactions, enhancing binding affinity to target proteins. Commonly employed in the preparation of small molecule drugs targeting neurological disorders and inflammatory diseases. Its nitro and piperidine functionalities allow for further chemical modi

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to engage in hydrogen bonding and π-π interactions, enhancing binding affinity to target proteins. Commonly employed in the preparation of small molecule drugs targeting neurological disorders and inflammatory diseases. Its nitro and piperidine functionalities allow for further chemical modifications, enabling the optimization of pharmacokinetic properties such as solubility and metabolic stability.

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