tert-butyl ((1-(4-chloro-2-fluorophenyl)cyclobutyl)methyl)carbamate

90%

Reagent Code: #241947

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.8 g/mol
Formula C₁₆H₂₁ClFNO₂
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 for targeted cancer therapies. Its structural features allow for selective modification in drug design, enhancing metabolic stability and bioavailability. Commonly employed in medicinal chemistry research to construct complex molecules requiring sterically hindered amine functionalities. Also utilized in the preparation of proteolysis-targeting chimeras (PROTACs) due to its favorable protecting group characteristics and compatibility with multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,340.00
inventory 250mg
10-20 days ฿6,930.00
inventory 1g
10-20 days ฿17,860.00

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tert-butyl ((1-(4-chloro-2-fluorophenyl)cyclobutyl)methyl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structural features allow for selective modification in drug design, enhancing metabolic stability and bioavailability. Commonly employed in medicinal chemistry research to construct complex molecules requiring sterically hindered amine functionalities. Also utilized in the preparation of proteolysis-targeting chimeras (PROTACs) due to its favorable

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structural features allow for selective modification in drug design, enhancing metabolic stability and bioavailability. Commonly employed in medicinal chemistry research to construct complex molecules requiring sterically hindered amine functionalities. Also utilized in the preparation of proteolysis-targeting chimeras (PROTACs) due to its favorable protecting group characteristics and compatibility with multi-step synthetic routes.

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