(3-Nitro-pyridin-2-yl)-piperidin-3-ylmethyl-aminehydrochloride

97%

Reagent Code: #219548
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CAS Number 1185319-15-6

science Other reagents with same CAS 1185319-15-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.731 g/mol
Formula C₁₁H₁₇ClN₄O₂
badge Registry Numbers
MDL Number MFCD09607823
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its nitrogen-rich heterocyclic structure, which enhances binding affinity to biological targets. Commonly employed in research settings for designing drugs that modulate enzyme activity, especially in oncology and inflammatory diseases. Its derivatives are explored for improved selectivity and potency in targeted therapies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,610.00
inventory 500mg
10-20 days ฿16,140.00
(3-Nitro-pyridin-2-yl)-piperidin-3-ylmethyl-aminehydrochloride
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its nitrogen-rich heterocyclic structure, which enhances binding affinity to biological targets. Commonly employed in research settings for designing drugs that modulate enzyme activity, especially in oncology and inflammatory diseases. Its derivatives are explored for improved selectivity and potency i

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its nitrogen-rich heterocyclic structure, which enhances binding affinity to biological targets. Commonly employed in research settings for designing drugs that modulate enzyme activity, especially in oncology and inflammatory diseases. Its derivatives are explored for improved selectivity and potency in targeted therapies.

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