tert-Butyl 4-(3-amino-6-((1S,3S,4S)-4-((tert-butyldimethylsilyl)oxy)-3-fluorocyclohexyl)pyrazin-2-yl)-2-fluorobenzoate

97%

Reagent Code: #113206
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CAS Number 1715032-87-3

science Other reagents with same CAS 1715032-87-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 519.70 g/mol
Formula C₂₇H₃₉F₂N₃O₃Si
badge Registry Numbers
MDL Number MFCD30609554
thermostat Physical Properties
Boiling Point 571.3±50.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This chemical is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex drug molecules. Its structure, featuring multiple functional groups such as amino, fluoro, and silyl-protected hydroxyl, makes it a valuable building block for the development of targeted therapies. It is often employed in the preparation of compounds designed for oncology and other therapeutic areas where precise molecular interactions are crucial. The presence of fluorine atoms enhances the metabolic stability and bioavailability of the resulting drugs, while the silyl protection allows for controlled deprotection during synthesis. Researchers leverage its versatility to create molecules with improved efficacy and reduced side effects, particularly in the design of kinase inhibitors and other small-molecule drugs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿954.00
inventory 250mg
10-20 days ฿1,935.00

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tert-Butyl 4-(3-amino-6-((1S,3S,4S)-4-((tert-butyldimethylsilyl)oxy)-3-fluorocyclohexyl)pyrazin-2-yl)-2-fluorobenzoate
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This chemical is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex drug molecules. Its structure, featuring multiple functional groups such as amino, fluoro, and silyl-protected hydroxyl, makes it a valuable building block for the development of targeted therapies. It is often employed in the preparation of compounds designed for oncology and other therapeutic areas where precise molecular interactions are crucial. The presence of fluorine atoms enhances the metabolic stability and bioavailability of the resulting drugs, while the silyl protection allows for controlled deprotection during synthesis. Researchers leverage its versatility to create molecules with improved efficacy and reduced side effects, particularly in the design of kinase inhibitors and other small-molecule drugs.
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