Benzyl (3-fluoro-4-(piperidin-1-yl)phenyl)carbamate

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Reagent Code: #150978
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CAS Number 172967-05-4

science Other reagents with same CAS 172967-05-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 328.38 g/mol
Formula C₁₉H₂₁FN₂O₂
badge Registry Numbers
MDL Number MFCD31803506
thermostat Physical Properties
Boiling Point 439.7±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.234±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting tyrosine kinases involved in cancer cell proliferation. It serves as a building block for compounds under investigation for oncology applications, including treatments for solid tumors. Its structure supports blood-brain barrier penetration, making it relevant in the development of central nervous system-targeted therapies. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates for improved potency and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,130.00
inventory 250mg
10-20 days ฿5,870.00
inventory 1g
10-20 days ฿11,740.00

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Benzyl (3-fluoro-4-(piperidin-1-yl)phenyl)carbamate
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting tyrosine kinases involved in cancer cell proliferation. It serves as a building block for compounds under investigation for oncology applications, including treatments for solid tumors. Its structure supports blood-brain barrier penetration, making it relevant in the development of central nervous system-targeted therapies. Also employed in medicinal chemistry for structure-activity relatio

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting tyrosine kinases involved in cancer cell proliferation. It serves as a building block for compounds under investigation for oncology applications, including treatments for solid tumors. Its structure supports blood-brain barrier penetration, making it relevant in the development of central nervous system-targeted therapies. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates for improved potency and selectivity.

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