tert-Butyl benzyloxycarbamate

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Reagent Code: #145974
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CAS Number 79722-21-7

science Other reagents with same CAS 79722-21-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.27 g/mol
Formula C₁₂H₁₇NO₃
badge Registry Numbers
MDL Number MFCD00191873
thermostat Physical Properties
Melting Point 45-47°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used as a protecting group for amines in organic synthesis, particularly in peptide and pharmaceutical manufacturing. Its stability under various reaction conditions makes it ideal for multi-step syntheses where selective deprotection is required. It is commonly employed in the production of active pharmaceutical ingredients (APIs) to mask amine functionality temporarily, allowing reactions to proceed at other sites without interference. The group can be removed under mild acidic conditions or via hydrogenolysis, offering flexibility in synthetic routes. It is also utilized in the preparation of intermediates for agrochemicals and fine chemicals due to its reliable performance and compatibility with a range of functional groups.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿630.00
inventory 25g
10-20 days ฿2,450.00
inventory 100g
10-20 days ฿9,610.00

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tert-Butyl benzyloxycarbamate
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Widely used as a protecting group for amines in organic synthesis, particularly in peptide and pharmaceutical manufacturing. Its stability under various reaction conditions makes it ideal for multi-step syntheses where selective deprotection is required. It is commonly employed in the production of active pharmaceutical ingredients (APIs) to mask amine functionality temporarily, allowing reactions to proceed at other sites without interference. The group can be removed under mild acidic conditions or via

Widely used as a protecting group for amines in organic synthesis, particularly in peptide and pharmaceutical manufacturing. Its stability under various reaction conditions makes it ideal for multi-step syntheses where selective deprotection is required. It is commonly employed in the production of active pharmaceutical ingredients (APIs) to mask amine functionality temporarily, allowing reactions to proceed at other sites without interference. The group can be removed under mild acidic conditions or via hydrogenolysis, offering flexibility in synthetic routes. It is also utilized in the preparation of intermediates for agrochemicals and fine chemicals due to its reliable performance and compatibility with a range of functional groups.

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