Tert-butyl (cis-4-(aminomethyl)cyclohexyl)carbamate

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Reagent Code: #242627
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CAS Number 509143-00-4

science Other reagents with same CAS 509143-00-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.33 g/mol
Formula C₁₂H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD03844602
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where protection of the amine group is required. Its structure allows for selective reactions in multi-step organic syntheses, especially in the preparation of biologically active compounds such as receptor agonists or enzyme inhibitors. Commonly employed in medicinal chemistry for constructing complex molecules with improved metabolic stability and target specificity. The tert-butyloxycarbonyl (Boc) protecting group enables controlled deprotection under mild acidic conditions, making it valuable in peptide and peptidomimetic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,510.00
inventory 250mg
10-20 days ฿3,440.00
inventory 1g
10-20 days ฿10,230.00
inventory 5g
10-20 days ฿41,190.00

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Tert-butyl (cis-4-(aminomethyl)cyclohexyl)carbamate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where protection of the amine group is required. Its structure allows for selective reactions in multi-step organic syntheses, especially in the preparation of biologically active compounds such as receptor agonists or enzyme inhibitors. Commonly employed in medicinal chemistry for constructing complex molecules with improved metabolic stability and target specificit

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where protection of the amine group is required. Its structure allows for selective reactions in multi-step organic syntheses, especially in the preparation of biologically active compounds such as receptor agonists or enzyme inhibitors. Commonly employed in medicinal chemistry for constructing complex molecules with improved metabolic stability and target specificity. The tert-butyloxycarbonyl (Boc) protecting group enables controlled deprotection under mild acidic conditions, making it valuable in peptide and peptidomimetic synthesis.

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