1-(Trifluoromethanesulfonyl)imidazole
≥98%
Reagent
Code: #114492
CAS Number
29540-81-6
blur_circular Chemical Specifications
scatter_plot
Molecular Information
Weight
200.14 g/mol
Formula
C₄H₃F₃N₂O₂S
badge
Registry Numbers
MDL Number
MFCD00037891
thermostat
Physical Properties
Boiling Point
40°C/10mmHg(lit.)
inventory_2
Storage & Handling
Storage
2-8°C
description Product Description
This chemical is widely used as a reagent in organic synthesis, particularly for introducing the trifluoromethanesulfonyl group into molecules, which is valuable in creating compounds with enhanced stability and reactivity. It is commonly employed in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals, where the triflyl group acts as a strong electron-withdrawing moiety. Additionally, it serves as a key intermediate in the synthesis of complex organic molecules, including heterocycles and biologically active compounds. Its ability to act as a triflating agent makes it useful in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds in advanced chemical processes.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Colorless to almost colorless clear liquid |
Purity (%) | 97.5-100% |
Infrared Spectrum | Conforms to Structure |
NMR | Conforms To Structure |
shopping_cart Available Sizes & Pricing
1-(Trifluoromethanesulfonyl)imidazole
This chemical is widely used as a reagent in organic synthesis, particularly for introducing the trifluoromethanesulfonyl group into molecules, which is valuable in creating compounds with enhanced stability and reactivity. It is commonly employed in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals, where the triflyl group acts as a strong electron-withdrawing moiety. Additionally, it serves as a key intermediate in the synthesis of complex organic molecules, including heterocycles and biologically active compounds. Its ability to act as a triflating agent makes it useful in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds in advanced chemical processes.
Mechanism | - |
Appearance | - |
Longevity | - |
Strength | - |
Storage | - |
Shelf Life | - |
Allergen(s) | - |
Dosage (Range) | - |
Recommended Dosage | - |
Dosage (Per Day) | - |
Recommended Dosage (Per Day) | - |
Mix Method | - |
Heat Resistance | - |
Stable in pH range | - |
Solubility | - |
Product Types | - |
INCI | - |
Purchase History for
Loading purchase history...
Cart
No products
Subtotal:
฿0.00
Total
฿0.00
THB