3-Amino-1H-pyrazolo[4,3-c]pyridin-4(5H)-one

95%

Reagent Code: #137069
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CAS Number 900863-27-6

science Other reagents with same CAS 900863-27-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.14 g/mol
Formula C₆H₆N₄O
badge Registry Numbers
MDL Number MFCD16877656
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as a key 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 ability to form hydrogen bonds and engage in π-π stacking interactions, enhancing binding affinity to target proteins. Also employed in the preparation of bioactive molecules with anti-inflammatory and neuroprotective properties. Its scaffold is explored in drug discovery programs for designing selective and potent therapeutic agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,550.00
inventory 1g
10-20 days ฿29,110.00

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3-Amino-1H-pyrazolo[4,3-c]pyridin-4(5H)-one
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Used as a key 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 ability to form hydrogen bonds and engage in π-π stacking interactions, enhancing binding affinity to target proteins. Also employed in the preparation of bioactive molecules with anti-inflammatory and neuroprotective properties. Its scaffold is explored in drug discovery programs for designing s

Used as a key 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 ability to form hydrogen bonds and engage in π-π stacking interactions, enhancing binding affinity to target proteins. Also employed in the preparation of bioactive molecules with anti-inflammatory and neuroprotective properties. Its scaffold is explored in drug discovery programs for designing selective and potent therapeutic agents.

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