tert-butyl ((4-(4-fluorophenyl)tetrahydro-2H-pyran-4-yl)methyl)carbamate

90%

Reagent Code: #195736

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.38 g/mol
Formula C₁₇H₂₄FNO₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports binding to specific enzyme targets, making it valuable in drug discovery for oncology and inflammatory diseases. The tert-butyl carbamate group acts as a protecting group for amines during multi-step syntheses, allowing selective reactivity. It is also employed in the preparation of bioactive molecules where the tetrahydropyran ring mimics natural product scaffolds, enhancing metabolic stability and solubility. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its favorable physicochemical properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿24,300.00
inventory 250mg
10-20 days ฿9,450.00

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tert-butyl ((4-(4-fluorophenyl)tetrahydro-2H-pyran-4-yl)methyl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports binding to specific enzyme targets, making it valuable in drug discovery for oncology and inflammatory diseases. The tert-butyl carbamate group acts as a protecting group for amines during multi-step syntheses, allowing selective reactivity. It is also employed in the preparation of bioactive molecules where the tetrahydropyran ring mimics natural product scaf

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports binding to specific enzyme targets, making it valuable in drug discovery for oncology and inflammatory diseases. The tert-butyl carbamate group acts as a protecting group for amines during multi-step syntheses, allowing selective reactivity. It is also employed in the preparation of bioactive molecules where the tetrahydropyran ring mimics natural product scaffolds, enhancing metabolic stability and solubility. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its favorable physicochemical properties.

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