(Trimethylsilyl)methyl Trifluoromethanesulfonate
≥98%
Reagent
Code: #113899
CAS Number
64035-64-9
blur_circular Chemical Specifications
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Molecular Information
Weight
236.28 g/mol
Formula
C₅H₁₁F₃O₃SSi
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Registry Numbers
MDL Number
MFCD00009914
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Storage & Handling
Storage
2-8°C, stored in inert gas
description Product Description
This chemical is widely used as a reagent in organic synthesis, particularly in the introduction of the trimethylsilyl group into various organic compounds. It is effective in silylation reactions, where it acts as a protecting group for alcohols, amines, and other functional groups, enhancing stability during complex chemical processes. Additionally, it is employed in the preparation of organosilicon compounds, which are valuable in the development of polymers, coatings, and adhesives. Its trifluoromethanesulfonate component also makes it a strong alkylating agent, useful in creating carbon-carbon bonds in synthetic pathways. This compound is particularly favored in the pharmaceutical and materials science industries for its efficiency and versatility in facilitating challenging chemical transformations.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Colorless to light yellow clear liquid |
Purity (%) | 98-100% |
Infrared Spectrum | Conforms To Structure |
High Boiling Impurity of Silylation Agent | No impurity higher than isopropyl myristate (≤50 ppm) after 5 min + hold-up time |
Agent | No impurity > Isopropyl myristate (≤50 ppm) after 5 min + hold up time |
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(Trimethylsilyl)methyl Trifluoromethanesulfonate
This chemical is widely used as a reagent in organic synthesis, particularly in the introduction of the trimethylsilyl group into various organic compounds. It is effective in silylation reactions, where it acts as a protecting group for alcohols, amines, and other functional groups, enhancing stability during complex chemical processes. Additionally, it is employed in the preparation of organosilicon compounds, which are valuable in the development of polymers, coatings, and adhesives. Its trifluoromethanesulfonate component also makes it a strong alkylating agent, useful in creating carbon-carbon bonds in synthetic pathways. This compound is particularly favored in the pharmaceutical and materials science industries for its efficiency and versatility in facilitating challenging chemical transformations.
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