N-Boc-(methylamino)acetaldehyde

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Reagent Code: #217146
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CAS Number 123387-72-4

science Other reagents with same CAS 123387-72-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.212 g/mol
Formula C₈H₁₅NO₃
badge Registry Numbers
MDL Number MFCD08064267
thermostat Physical Properties
Boiling Point 218.2±19.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.026 g/cm3
Storage -20°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where protected amino aldehyde functionalities are required. Its aldehyde group enables coupling reactions such as reductive amination, while the Boc-protected methylamino group ensures stability and selectivity during multi-step syntheses. Commonly employed in the preparation of complex molecules including protease inhibitors, kinase inhibitors, and other bioactive compounds. Its structure allows for selective deprotection and further functionalization, making it valuable in medicinal chemistry and drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿850.00
inventory 10g
10-20 days ฿1,680.00
inventory 100g
10-20 days ฿14,020.00
inventory 250g
10-20 days ฿31,920.00
inventory 25g
10-20 days ฿3,760.00

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N-Boc-(methylamino)acetaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where protected amino aldehyde functionalities are required. Its aldehyde group enables coupling reactions such as reductive amination, while the Boc-protected methylamino group ensures stability and selectivity during multi-step syntheses. Commonly employed in the preparation of complex molecules including protease inhibitors, kinase inhibitors, and other bioactive

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where protected amino aldehyde functionalities are required. Its aldehyde group enables coupling reactions such as reductive amination, while the Boc-protected methylamino group ensures stability and selectivity during multi-step syntheses. Commonly employed in the preparation of complex molecules including protease inhibitors, kinase inhibitors, and other bioactive compounds. Its structure allows for selective deprotection and further functionalization, making it valuable in medicinal chemistry and drug discovery.

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