tert-Butyl N-[trans-4-amino-1-methylcyclohexyl]carbamate

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Reagent Code: #141158
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CAS Number 412293-46-0

science Other reagents with same CAS 412293-46-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.33 g/mol
Formula C₁₂H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD30333484
thermostat Physical Properties
Boiling Point 325.9±31.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.01±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring sterically hindered amine functionalities. Its protected amine group allows for selective reactions in multi-step organic syntheses, especially in the preparation of kinase inhibitors and other bioactive molecules. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions and can be easily removed under mild acidic conditions, making it ideal for use in peptide chemistry and medicinal chemistry routes. Commonly employed in the production of central nervous system (CNS) agents and anti-inflammatory drugs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,920.00
inventory 1g
10-20 days ฿39,590.00
inventory 500mg
10-20 days ฿26,370.00

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tert-Butyl N-[trans-4-amino-1-methylcyclohexyl]carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring sterically hindered amine functionalities. Its protected amine group allows for selective reactions in multi-step organic syntheses, especially in the preparation of kinase inhibitors and other bioactive molecules. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions and can be easily removed under mild acidic conditi
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring sterically hindered amine functionalities. Its protected amine group allows for selective reactions in multi-step organic syntheses, especially in the preparation of kinase inhibitors and other bioactive molecules. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions and can be easily removed under mild acidic conditions, making it ideal for use in peptide chemistry and medicinal chemistry routes. Commonly employed in the production of central nervous system (CNS) agents and anti-inflammatory drugs.
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