3-(6-Bromo-pyridin-2-yloxy)-piperidine-1-carboxylicacidtert-butylester

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Reagent Code: #152192
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CAS Number 1065484-39-0

science Other reagents with same CAS 1065484-39-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 357.243 g/mol
Formula C₁₅H₂₁BrN₂O₃
badge Registry Numbers
MDL Number MFCD10698905
thermostat Physical Properties
Boiling Point 416.4±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.355 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of complex heterocyclic systems important in drug discovery. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance binding affinity and selectivity toward target enzymes. Also utilized in research settings to prepare analogs for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿19,750.00

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3-(6-Bromo-pyridin-2-yloxy)-piperidine-1-carboxylicacidtert-butylester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of complex heterocyclic systems important in drug discovery. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance binding affinity and selectivity toward target enzymes. Also utilized in research settings to prepare analogs for structure-activity relationship (SAR) studies.

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of complex heterocyclic systems important in drug discovery. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance binding affinity and selectivity toward target enzymes. Also utilized in research settings to prepare analogs for structure-activity relationship (SAR) studies.

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