Ethyl 1-(pyridin-4-yl)-1H-pyrazole-4-carboxylate

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Reagent Code: #180601
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CAS Number 1014631-92-5

science Other reagents with same CAS 1014631-92-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.22 g/mol
Formula C₁₁H₁₁N₃O₂
badge Registry Numbers
MDL Number MFCD20275539
thermostat Physical Properties
Boiling Point 361.6±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.23±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in medicinal chemistry for designing drugs with high selectivity. Also employed in agrochemical research for developing new pesticides due to its ability to modulate biological activity in target organisms. Commonly utilized in combinatorial chemistry and high-throughput screening for lead compound optimization.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿25,260.00
inventory 5g
10-20 days ฿88,400.00

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Ethyl 1-(pyridin-4-yl)-1H-pyrazole-4-carboxylate
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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. Its structure supports binding to enzyme active sites, making it valuable in medicinal chemistry for designing drugs with high selectivity. Also employed in agrochemical research for developing new pesticides due to its ability to modulate biological activity in target organisms. Commonly utilized in combinatorial chemistry and high-throughput screening for lead

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in medicinal chemistry for designing drugs with high selectivity. Also employed in agrochemical research for developing new pesticides due to its ability to modulate biological activity in target organisms. Commonly utilized in combinatorial chemistry and high-throughput screening for lead compound optimization.

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