1H-Pyrazolo[4,3-c]pyridin-4-amine

≥95%

Reagent Code: #196793
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CAS Number 1159829-57-8

science Other reagents with same CAS 1159829-57-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 134.142 g/mol
Formula C₆H₆N₄
badge Registry Numbers
MDL Number MFCD12400993
thermostat Physical Properties
Boiling Point 416.4±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.480±0.06 g/cm3(Predicted)
Storage 2-8°C, avoiding light

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 scaffold in medicinal chemistry due to its ability to mimic purine bases, enabling interaction with biological targets such as ATP-binding sites in enzymes. Its derivatives are explored for anti-inflammatory, antiviral, and neuroprotective activities. Also employed in research for designing selective inhibitors in signal transduction pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,600.00
inventory 250mg
10-20 days ฿21,030.00
inventory 1g
10-20 days ฿34,130.00

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1H-Pyrazolo[4,3-c]pyridin-4-amine
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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 scaffold in medicinal chemistry due to its ability to mimic purine bases, enabling interaction with biological targets such as ATP-binding sites in enzymes. Its derivatives are explored for anti-inflammatory, antiviral, and neuroprotective activities. Also employed in research for designing selective inhibitors in signal transduction pathways.

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 scaffold in medicinal chemistry due to its ability to mimic purine bases, enabling interaction with biological targets such as ATP-binding sites in enzymes. Its derivatives are explored for anti-inflammatory, antiviral, and neuroprotective activities. Also employed in research for designing selective inhibitors in signal transduction pathways.

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