1H-Pyrazolo[3,4-b]pyrazine-3-carboxylic acid

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Reagent Code: #197713
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CAS Number 1286754-47-9

science Other reagents with same CAS 1286754-47-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.12 g/mol
Formula C₆H₄N₄O₂
badge Registry Numbers
MDL Number MFCD27987648
thermostat Physical Properties
Boiling Point 493.8±40.0 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting cancer-related enzymes. Its structure supports the development of compounds with high selectivity and potency in cell signaling pathways. Also explored in agrochemicals for designing novel pesticides due to its ability to interact with biological targets in pests. Commonly employed in medicinal chemistry for scaffold modification to enhance drug-like properties such as solubility and metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿44,000.00
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1H-Pyrazolo[3,4-b]pyrazine-3-carboxylic acid
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting cancer-related enzymes. Its structure supports the development of compounds with high selectivity and potency in cell signaling pathways. Also explored in agrochemicals for designing novel pesticides due to its ability to interact with biological targets in pests. Commonly employed in medicinal chemistry for scaffold modification to enhance drug-like properties such as solubility and me

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting cancer-related enzymes. Its structure supports the development of compounds with high selectivity and potency in cell signaling pathways. Also explored in agrochemicals for designing novel pesticides due to its ability to interact with biological targets in pests. Commonly employed in medicinal chemistry for scaffold modification to enhance drug-like properties such as solubility and metabolic stability.

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