N-(tert-Butoxycarbonyloxy)succinimide

98%

Reagent Code: #60103
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Alias Boc-OSu
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CAS Number 13139-12-3

science Other reagents with same CAS 13139-12-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.20 g/mol
Formula C₉H₁₃NO₅
badge Registry Numbers
EC Number 236-071-1
MDL Number MFCD00037903
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This chemical is widely used as a protecting agent in organic synthesis, particularly for amino groups. It is employed to introduce the tert-butoxycarbonyl (Boc) group, which shields amines during reactions that might otherwise affect them. This protection is crucial in peptide synthesis, where it allows for the selective formation of peptide bonds without unwanted side reactions. After the desired reactions are complete, the Boc group can be easily removed under mild acidic conditions, restoring the original amino group. Its stability and ease of removal make it a valuable tool in the development of pharmaceuticals, agrochemicals, and complex organic molecules.

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Test Parameter Specification
Purity 97.5-100%

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿2,940.00
inventory 1g
10-20 days ฿400.00
inventory 5g
10-20 days ฿900.00

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N-(tert-Butoxycarbonyloxy)succinimide
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This chemical is widely used as a protecting agent in organic synthesis, particularly for amino groups. It is employed to introduce the tert-butoxycarbonyl (Boc) group, which shields amines during reactions that might otherwise affect them. This protection is crucial in peptide synthesis, where it allows for the selective formation of peptide bonds without unwanted side reactions. After the desired reactions are complete, the Boc group can be easily removed under mild acidic conditions, restoring the ori

This chemical is widely used as a protecting agent in organic synthesis, particularly for amino groups. It is employed to introduce the tert-butoxycarbonyl (Boc) group, which shields amines during reactions that might otherwise affect them. This protection is crucial in peptide synthesis, where it allows for the selective formation of peptide bonds without unwanted side reactions. After the desired reactions are complete, the Boc group can be easily removed under mild acidic conditions, restoring the original amino group. Its stability and ease of removal make it a valuable tool in the development of pharmaceuticals, agrochemicals, and complex organic molecules.

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