Isopropyl 4-(1H-pyrazol-4-yl)piperidine-1-carboxylate

95%

Reagent Code: #198587
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CAS Number 1245645-53-7

science Other reagents with same CAS 1245645-53-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.3 g/mol
Formula C₁₂H₁₉N₃O₂
badge Registry Numbers
MDL Number MFCD12911420
thermostat Physical Properties
Boiling Point 402.0±38.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.161 g/cm3
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of treatments for inflammatory diseases and certain cancers due to its ability to modulate signaling pathways. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies involving pyrazole and piperidine derivatives. Its carboxylate ester group allows for easy modification, making it valuable in drug design and optimization.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿14,590.00
1g
10-20 days ฿66,910.00
Isopropyl 4-(1H-pyrazol-4-yl)piperidine-1-carboxylate
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of treatments for inflammatory diseases and certain cancers due to its ability to modulate signaling pathways. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies involving pyrazole and piperidine derivatives. Its carboxylate ester group allows for easy modification, making it valuable in drug design

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of treatments for inflammatory diseases and certain cancers due to its ability to modulate signaling pathways. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies involving pyrazole and piperidine derivatives. Its carboxylate ester group allows for easy modification, making it valuable in drug design and optimization.

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