1-Benzyl-3-((dimethylcarbamoyl)oxy)pyridin-1-ium bromide

≥95%

Reagent Code: #126275
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CAS Number 587-46-2

science Other reagents with same CAS 587-46-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.21 g/mol
Formula C15H17BrN2O2
badge Registry Numbers
MDL Number MFCD00867184
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in organic synthesis as a reagent for introducing the benzyl group into various molecules. It is particularly effective in reactions where selective benzylation is required, such as in the modification of nucleosides, nucleotides, and other heterocyclic compounds. Additionally, it finds application in the preparation of pharmaceutical intermediates, where the benzyl group acts as a protecting group for functional groups like alcohols, amines, and carboxylic acids. Its use is also observed in the development of ionic liquids and as a catalyst or co-catalyst in certain chemical transformations.

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Test Parameter Specification
Appearance White to off-white to yellow solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,807.00
inventory 250mg
10-20 days ฿19,710.00
inventory 1g
10-20 days ฿31,350.00

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1-Benzyl-3-((dimethylcarbamoyl)oxy)pyridin-1-ium bromide
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This compound is primarily used in organic synthesis as a reagent for introducing the benzyl group into various molecules. It is particularly effective in reactions where selective benzylation is required, such as in the modification of nucleosides, nucleotides, and other heterocyclic compounds. Additionally, it finds application in the preparation of pharmaceutical intermediates, where the benzyl group acts as a protecting group for functional groups like alcohols, amines, and carboxylic acids. Its use

This compound is primarily used in organic synthesis as a reagent for introducing the benzyl group into various molecules. It is particularly effective in reactions where selective benzylation is required, such as in the modification of nucleosides, nucleotides, and other heterocyclic compounds. Additionally, it finds application in the preparation of pharmaceutical intermediates, where the benzyl group acts as a protecting group for functional groups like alcohols, amines, and carboxylic acids. Its use is also observed in the development of ionic liquids and as a catalyst or co-catalyst in certain chemical transformations.

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