Ethyl 1-(2-((tert-butoxycarbonyl)amino)ethyl)-3-(4-chlorophenyl)-4-(((trifluoromethyl)sulfonyl)oxy)-1H-pyrazole-5-carboxylate

≥95%

Reagent Code: #184741
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CAS Number 1956364-75-2

science Other reagents with same CAS 1956364-75-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 541.93 g/mol
Formula C₂₀H₂₃ClF₃N₃O₇S
badge Registry Numbers
MDL Number MFCD28991975
thermostat Physical Properties
Boiling Point 632.8±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.43±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors and anti-inflammatory agents. Its structure allows for selective modification, making it valuable in developing drug candidates with improved potency and metabolic stability. Commonly employed in cross-coupling reactions due to the trifluoromethylsulfonyl oxy group, enabling carbon–carbon bond formation in complex molecule assembly. Also utilized in the preparation of pyrazole-based derivatives for studies in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,690.00
inventory 250mg
10-20 days ฿23,620.00

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Ethyl 1-(2-((tert-butoxycarbonyl)amino)ethyl)-3-(4-chlorophenyl)-4-(((trifluoromethyl)sulfonyl)oxy)-1H-pyrazole-5-carboxylate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors and anti-inflammatory agents. Its structure allows for selective modification, making it valuable in developing drug candidates with improved potency and metabolic stability. Commonly employed in cross-coupling reactions due to the trifluoromethylsulfonyl oxy group, enabling carbon–carbon bond formation in complex molecule assembly. Also utilized in the preparatio

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors and anti-inflammatory agents. Its structure allows for selective modification, making it valuable in developing drug candidates with improved potency and metabolic stability. Commonly employed in cross-coupling reactions due to the trifluoromethylsulfonyl oxy group, enabling carbon–carbon bond formation in complex molecule assembly. Also utilized in the preparation of pyrazole-based derivatives for studies in medicinal chemistry.

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