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Trifluoromethanesulphonamide
[CAS# 421-85-2]

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Complete supplier list of Trifluoromethanesulphonamide
Identification
Classification Organic raw materials >> Amino compound >> Amide compound
Name Trifluoromethanesulphonamide
Synonyms triflimidic acid
Molecular Structure CAS # 421-85-2, Trifluoromethanesulphonamide, triflimidic acid
Molecular Formula CH2F3NO2S
Molecular Weight 149.09
CAS Registry Number 421-85-2
EC Number 627-705-1
SMILES C(F)(F)(F)S(=O)(=O)N
Properties
Melting point 120-124 ºC
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H302-H315-H319-H335    Details
Precautionary Statements P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Acute toxicityAcute Tox.4H302
Specific target organ toxicity - single exposureSTOT SE3H335
Eye irritationEye Irrit.2H319
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.4H312
Eye irritationEye Irrit.2AH319
SDS Available
up Discovory and Applicatios
Trifluoromethanesulphonamide, with the chemical formula CF3SO2NH2, is an organofluorine compound characterized by the presence of a trifluoromethyl group attached to a sulphonamide moiety. This compound is recognized for its unique chemical properties and diverse applications in organic synthesis and material science.

The discovery of trifluoromethanesulphonamide emerged from the broader study of sulphonamide derivatives and their potential applications. The trifluoromethyl group, known for its electron-withdrawing properties, enhances the reactivity of the sulphonamide functionality. The synthesis of trifluoromethanesulphonamide involves the reaction of trifluoromethylsulphonyl chloride with ammonia or primary amines. This process provides a straightforward route to obtain the trifluoromethanesulphonamide with high purity.

In organic synthesis, trifluoromethanesulphonamide is widely used as a reagent and catalyst. Its strong electron-withdrawing trifluoromethyl group makes it an effective electrophile in various chemical reactions. For instance, it can participate in nucleophilic substitution reactions where it acts as a sulphonamide donor, facilitating the formation of new carbon-nitrogen bonds. Additionally, it is employed in the synthesis of complex molecules and pharmaceuticals due to its ability to modify functional groups and enhance reaction selectivity.

The compound also finds applications in materials science, particularly in the development of fluorinated polymers and advanced materials. Trifluoromethanesulphonamide can be used to introduce trifluoromethyl groups into polymers, imparting unique properties such as increased hydrophobicity and chemical resistance. These modified polymers are valuable in various industrial applications, including coatings, adhesives, and membranes.

Moreover, trifluoromethanesulphonamide is utilized in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Its reactivity allows for the introduction of trifluoromethyl groups into drug molecules, which can enhance their biological activity and stability. Research continues to explore its potential in the development of new therapeutic agents and advanced drug delivery systems.

In summary, trifluoromethanesulphonamide is a versatile chemical compound with significant applications in organic synthesis, materials science, and pharmaceuticals. Its unique chemical properties make it a valuable reagent and catalyst in various chemical transformations and material modifications.
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