Dibenzyl Dicarbonate

≥97%

Reagent Code: #60116
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CAS Number 31139-36-3

science Other reagents with same CAS 31139-36-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.28 g/mol
Formula C₁₆H₁₄O₅
badge Registry Numbers
MDL Number MFCD00043124
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Dibenzyl dicarbonate is primarily used as a protecting agent in organic synthesis, particularly for alcohols and amines. It acts as a benzyloxycarbonyl (Cbz) group donor, which helps shield reactive functional groups during complex chemical reactions. This allows chemists to selectively modify other parts of a molecule without interference. It is commonly employed in peptide synthesis to protect amino groups, ensuring the desired sequence is achieved. Additionally, it finds application in the preparation of pharmaceuticals and fine chemicals, where precise control over molecular structure is critical. Its stability and ease of removal under mild conditions make it a valuable tool in synthetic chemistry.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity 97-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,360.00
inventory 5g
10-20 days ฿9,950.00

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Dibenzyl Dicarbonate
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Dibenzyl dicarbonate is primarily used as a protecting agent in organic synthesis, particularly for alcohols and amines. It acts as a benzyloxycarbonyl (Cbz) group donor, which helps shield reactive functional groups during complex chemical reactions. This allows chemists to selectively modify other parts of a molecule without interference. It is commonly employed in peptide synthesis to protect amino groups, ensuring the desired sequence is achieved. Additionally, it finds application in the preparation

Dibenzyl dicarbonate is primarily used as a protecting agent in organic synthesis, particularly for alcohols and amines. It acts as a benzyloxycarbonyl (Cbz) group donor, which helps shield reactive functional groups during complex chemical reactions. This allows chemists to selectively modify other parts of a molecule without interference. It is commonly employed in peptide synthesis to protect amino groups, ensuring the desired sequence is achieved. Additionally, it finds application in the preparation of pharmaceuticals and fine chemicals, where precise control over molecular structure is critical. Its stability and ease of removal under mild conditions make it a valuable tool in synthetic chemistry.

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