Tert-butyl 4-aminocyclohexylcarbamate

95%

Reagent Code: #240268
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CAS Number 195314-59-1

science Other reagents with same CAS 195314-59-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.31 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD01076211
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring protected amine functionalities. Its structure allows for selective reactions at the amino group while the tert-butyl carbamate (Boc) group remains stable under various conditions, enabling stepwise construction of complex molecules. Commonly employed in the synthesis of kinase inhibitors and other bioactive compounds where a cyclohexyl linker with dual amine functions is needed. The compound’s stability and solubility profile make it suitable for solid-phase and solution-phase peptide-like synthesis. It is also utilized in medicinal chemistry for scaffold modification to improve metabolic stability and binding affinity in drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿460.00
inventory 5g
10-20 days ฿2,060.00
inventory 25g
10-20 days ฿9,380.00

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Tert-butyl 4-aminocyclohexylcarbamate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring protected amine functionalities. Its structure allows for selective reactions at the amino group while the tert-butyl carbamate (Boc) group remains stable under various conditions, enabling stepwise construction of complex molecules. Commonly employed in the synthesis of kinase inhibitors and other bioactive compounds where a cyclohexyl linker with dual amine function

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring protected amine functionalities. Its structure allows for selective reactions at the amino group while the tert-butyl carbamate (Boc) group remains stable under various conditions, enabling stepwise construction of complex molecules. Commonly employed in the synthesis of kinase inhibitors and other bioactive compounds where a cyclohexyl linker with dual amine functions is needed. The compound’s stability and solubility profile make it suitable for solid-phase and solution-phase peptide-like synthesis. It is also utilized in medicinal chemistry for scaffold modification to improve metabolic stability and binding affinity in drug candidates.

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