Ethyl 6-cyclopropylpyrazolo[1,5-a]pyrimidine-3-carboxylate

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Reagent Code: #58912
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CAS Number 1956363-80-6

science Other reagents with same CAS 1956363-80-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.25 g/mol
Formula C₁₂H₁₃N₃O₂
badge Registry Numbers
MDL Number MFCD29917102
inventory_2 Storage & Handling
Density 1.41±0.1 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It serves as a building block for the development of potential therapeutic agents, particularly in the design of inhibitors targeting specific enzymes or receptors. Its pyrazolo[1,5-a]pyrimidine core structure is of significant interest due to its ability to mimic purine bases, making it valuable in the creation of compounds with potential anticancer, anti-inflammatory, or antiviral properties. Additionally, its cyclopropyl group can enhance metabolic stability and influence the pharmacokinetic profile of the resulting drug candidates. Researchers often employ this compound in early-stage drug discovery to explore structure-activity relationships and optimize lead compounds for further development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,374.00
inventory 250mg
10-20 days ฿23,400.00
inventory 1g
10-20 days ฿46,800.00

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Ethyl 6-cyclopropylpyrazolo[1,5-a]pyrimidine-3-carboxylate
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It serves as a building block for the development of potential therapeutic agents, particularly in the design of inhibitors targeting specific enzymes or receptors. Its pyrazolo[1,5-a]pyrimidine core structure is of significant interest due to its ability to mimic purine bases, making it valuable in the creation of compounds with potential anticancer, anti-infla

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It serves as a building block for the development of potential therapeutic agents, particularly in the design of inhibitors targeting specific enzymes or receptors. Its pyrazolo[1,5-a]pyrimidine core structure is of significant interest due to its ability to mimic purine bases, making it valuable in the creation of compounds with potential anticancer, anti-inflammatory, or antiviral properties. Additionally, its cyclopropyl group can enhance metabolic stability and influence the pharmacokinetic profile of the resulting drug candidates. Researchers often employ this compound in early-stage drug discovery to explore structure-activity relationships and optimize lead compounds for further development.

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