5,7-Diphenylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid

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Reagent Code: #178592
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CAS Number 352208-55-0

science Other reagents with same CAS 352208-55-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.33 g/mol
Formula C₁₉H₁₃N₃O₂
badge Registry Numbers
MDL Number MFCD01527942
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. It exhibits utility in medicinal chemistry due to its ability to modulate biological targets involved in cell signaling pathways. Its structural framework supports binding to ATP sites in kinases, making it valuable in designing drugs for oncology and inflammatory diseases. Also employed in research settings to explore structure-activity relationships in heterocyclic compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,970.00
inventory 250mg
10-20 days ฿4,830.00
inventory 1g
10-20 days ฿15,600.00

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5,7-Diphenylpyrazolo[1,5-a]pyrimidine-3-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 therapy. It exhibits utility in medicinal chemistry due to its ability to modulate biological targets involved in cell signaling pathways. Its structural framework supports binding to ATP sites in kinases, making it valuable in designing drugs for oncology and inflammatory diseases. Also employed in research settings to explore structure-activity relationships in heterocyc

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. It exhibits utility in medicinal chemistry due to its ability to modulate biological targets involved in cell signaling pathways. Its structural framework supports binding to ATP sites in kinases, making it valuable in designing drugs for oncology and inflammatory diseases. Also employed in research settings to explore structure-activity relationships in heterocyclic compounds.

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