Tert-butyl methylcarbamate

≥95%

Reagent Code: #240279
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CAS Number 16066-84-5

science Other reagents with same CAS 16066-84-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 131.17 g/mol
Formula C₆H₁₃NO₂
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MDL Number MFCD08899404
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Tert-butyl methylcarbamate is the tert-butyloxycarbonyl (Boc)-protected form of methylamine, serving as a key intermediate in organic synthesis. It is widely used in the pharmaceutical industry for the preparation of active pharmaceutical ingredients (APIs), including sartans like losartan, where the protected amine prevents side reactions during multi-step processes. The Boc group is introduced to shield the nitrogen and can be selectively removed under mild acidic conditions, such as with trifluoroacetic acid (TFA) or HCl in dioxane, facilitating complex molecule assembly. Its compatibility with various functional groups enhances flexibility in synthetic routes. Additionally, it is employed in the synthesis of agrochemicals and fine chemicals as a building block.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿162.00
inventory 5g
10-20 days ฿330.00
inventory 25g
10-20 days ฿1,600.00
inventory 100g
10-20 days ฿6,140.00
Tert-butyl methylcarbamate
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Tert-butyl methylcarbamate is the tert-butyloxycarbonyl (Boc)-protected form of methylamine, serving as a key intermediate in organic synthesis. It is widely used in the pharmaceutical industry for the preparation of active pharmaceutical ingredients (APIs), including sartans like losartan, where the protected amine prevents side reactions during multi-step processes. The Boc group is introduced to shield the nitrogen and can be selectively removed under mild acidic conditions, such as with trifluoroacet

Tert-butyl methylcarbamate is the tert-butyloxycarbonyl (Boc)-protected form of methylamine, serving as a key intermediate in organic synthesis. It is widely used in the pharmaceutical industry for the preparation of active pharmaceutical ingredients (APIs), including sartans like losartan, where the protected amine prevents side reactions during multi-step processes. The Boc group is introduced to shield the nitrogen and can be selectively removed under mild acidic conditions, such as with trifluoroacetic acid (TFA) or HCl in dioxane, facilitating complex molecule assembly. Its compatibility with various functional groups enhances flexibility in synthetic routes. Additionally, it is employed in the synthesis of agrochemicals and fine chemicals as a building block.

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