tert-Butyl methyl(3-nitrophenyl)carbamate

95%

Reagent Code: #141264
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CAS Number 528882-15-7

science Other reagents with same CAS 528882-15-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.2664 g/mol
Formula C₁₂H₁₆N₂O₄
badge Registry Numbers
MDL Number MFCD11111482
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protected amine derivative, allowing selective reactions at other functional sites in complex molecule assembly. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions and can be removed under mild acidic conditions, making it valuable in multi-step synthesis. The presence of the nitro group enables further transformations such as reduction to an amine, facilitating the construction of nitrogen-containing compounds. Commonly employed in the development of bioactive molecules where controlled reactivity and functional group compatibility are essential.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,510.00
inventory 250mg
10-20 days ฿11,040.00
inventory 1g
10-20 days ฿29,830.00

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tert-Butyl methyl(3-nitrophenyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protected amine derivative, allowing selective reactions at other functional sites in complex molecule assembly. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions and can be removed under mild acidic conditions, making it valuable in multi-step synthesis. The presence of the nitro group enables further transformations such as reduction

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protected amine derivative, allowing selective reactions at other functional sites in complex molecule assembly. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions and can be removed under mild acidic conditions, making it valuable in multi-step synthesis. The presence of the nitro group enables further transformations such as reduction to an amine, facilitating the construction of nitrogen-containing compounds. Commonly employed in the development of bioactive molecules where controlled reactivity and functional group compatibility are essential.

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