3-Methyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid

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Reagent Code: #203044
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CAS Number 1118787-14-6

science Other reagents with same CAS 1118787-14-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.16 g/mol
Formula C₈H₇N₃O₂
badge Registry Numbers
MDL Number MFCD11857900
thermostat Physical Properties
Melting Point >350 °C
Boiling Point 468.8±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.512±0.06 g/cm3(Predicted)
Storage 2-8°C

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 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 antiviral properties. Its structural features make it valuable in optimizing drug candidates for improved metabolic stability and solubility.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,460.00
inventory 500mg
10-20 days ฿15,370.00

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3-Methyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid
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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 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 antiviral properties. Its structural features make it valuable in optimizing drug candidates for i

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 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 antiviral properties. Its structural features make it valuable in optimizing drug candidates for improved metabolic stability and solubility.

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