tert-Butyl 4-(6-fluoro-1H-indazol-3-yl)piperidine-1-carboxylate

95%

Reagent Code: #152302
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CAS Number 1198284-41-1

science Other reagents with same CAS 1198284-41-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.37 g/mol
Formula C₁₇H₂₂FN₃O₂
badge Registry Numbers
MDL Number MFCD12912620
thermostat Physical Properties
Boiling Point 470.2±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.234±0.06 g/cm3(Predicted)
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports the development of agents with potential anticancer and anti-inflammatory properties. The presence of the fluoroindazole moiety enhances binding affinity to certain enzyme targets, making it valuable in drug discovery. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid piperidine-indazole framework.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,080.00
inventory 250mg
10-20 days ฿19,800.00
inventory 1g
10-20 days ฿62,330.00

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tert-Butyl 4-(6-fluoro-1H-indazol-3-yl)piperidine-1-carboxylate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports the development of agents with potential anticancer and anti-inflammatory properties. The presence of the fluoroindazole moiety enhances binding affinity to certain enzyme targets, making it valuable in drug discovery. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid piperidine-inda

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports the development of agents with potential anticancer and anti-inflammatory properties. The presence of the fluoroindazole moiety enhances binding affinity to certain enzyme targets, making it valuable in drug discovery. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid piperidine-indazole framework.

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