1-Carbobenzoxy-3-methylimidazolium Trifluoromethanesulfonate

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Reagent Code: #73263
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CAS Number 163080-99-7

science Other reagents with same CAS 163080-99-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 366.31 g/mol
Formula C₁₃H₁₃F₃N₂O₅S
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used in organic synthesis as a reagent for the protection of amino groups. It facilitates the formation of carbamate esters, which are crucial intermediates in peptide synthesis. The compound is particularly valued for its ability to provide a stable protecting group that can be easily removed under mild conditions, making it highly useful in the production of complex organic molecules, including pharmaceuticals and bioactive compounds. Its trifluoromethanesulfonate component enhances its reactivity, enabling efficient transformations in various chemical reactions. This makes it a versatile tool in the development of new drugs and other fine chemicals.

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Test Parameter Specification
Appearance White to Almost White Powder to Crystal
Purity (%) 98-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿2,601.00

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1-Carbobenzoxy-3-methylimidazolium Trifluoromethanesulfonate
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This chemical is primarily used in organic synthesis as a reagent for the protection of amino groups. It facilitates the formation of carbamate esters, which are crucial intermediates in peptide synthesis. The compound is particularly valued for its ability to provide a stable protecting group that can be easily removed under mild conditions, making it highly useful in the production of complex organic molecules, including pharmaceuticals and bioactive compounds. Its trifluoromethanesulfonate component e

This chemical is primarily used in organic synthesis as a reagent for the protection of amino groups. It facilitates the formation of carbamate esters, which are crucial intermediates in peptide synthesis. The compound is particularly valued for its ability to provide a stable protecting group that can be easily removed under mild conditions, making it highly useful in the production of complex organic molecules, including pharmaceuticals and bioactive compounds. Its trifluoromethanesulfonate component enhances its reactivity, enabling efficient transformations in various chemical reactions. This makes it a versatile tool in the development of new drugs and other fine chemicals.

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