Tert-butyl(2-amino-6-fluorophenyl)carbamate

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Reagent Code: #244307
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CAS Number 954239-11-3

science Other reagents with same CAS 954239-11-3

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scatter_plot Molecular Information
Weight 226.25 g/mol
Formula C₁₁H₁₅FN₂O₂
badge Registry Numbers
MDL Number MFCD09701254
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug discovery. Commonly employed in the preparation of tyrosine kinase inhibitors and analogs used in cancer research. Also utilized in the construction of fluorinated aromatic scaffolds to enhance metabolic stability and binding affinity in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,130.00
inventory 250mg
10-20 days ฿6,400.00
inventory 1g
10-20 days ฿21,110.00

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Tert-butyl(2-amino-6-fluorophenyl)carbamate
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Used as an intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug discovery. Commonly employed in the preparation of tyrosine kinase inhibitors and analogs used in cancer research. Also utilized in the construction of fluorinated aromatic scaffolds to enhance metabolic stability an

Used as an intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug discovery. Commonly employed in the preparation of tyrosine kinase inhibitors and analogs used in cancer research. Also utilized in the construction of fluorinated aromatic scaffolds to enhance metabolic stability and binding affinity in medicinal chemistry.

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