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65007-00-3

Pyridin-2-yl trifluoromethanesulfonate

Catalog#: AR003IM8  |   CAS#: 65007-00-3  |   MDL#: MFCD00192531  |   MF: C6H4F3NO3S  |   MW: 227.1611

Packsize Purity Price Availability Quantity
1g 98% $14.00 Global Stock Buy Now Add To Cart
5g 98% $48.00 Global Stock Buy Now Add To Cart
10g 98% $90.00 Global Stock Buy Now Add To Cart
25g 98% $170.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003IM8
Chemical Name Pyridin-2-yl trifluoromethanesulfonate
CAS Number 65007-00-3
Molecular Formula C6H4F3NO3S
Molecular Weight 227.1611
MDL Number MFCD00192531
SMILES O=S(=O)(C(F)(F)F)Oc1ccccn1

Pyridin-2-yl trifluoromethanesulfonate is a versatile chemical reagent commonly used in chemical synthesis as a powerful and efficient electrophilic trifluoromethanesulfonylating agent. Its unique structure allows for selective introduction of the trifluoromethanesulfonyl group onto nucleophilic substrates, enabling the synthesis of various valuable compounds with enhanced physicochemical properties.In organic synthesis, Pyridin-2-yl trifluoromethanesulfonate can be employed in the functionalization of a wide range of nucleophiles, including alcohols, amines, and thiols, to produce trifluoromethanesulfonate esters, sulfonamides, and sulfides, respectively. This reagent offers distinct advantages such as high reactivity, mild reaction conditions, and good functional group tolerance, making it an attractive option for the modification of complex molecules.Furthermore, Pyridin-2-yl trifluoromethanesulfonate has found applications in the pharmaceutical industry for the synthesis of drug candidates and bioactive compounds due to the trifluoromethanesulfonyl group's ability to enhance the pharmacokinetic and pharmacodynamic properties of the target molecules. Its utility in medicinal chemistry has contributed to the development of novel pharmaceuticals with improved potency, metabolic stability, and bioavailability.Overall, Pyridin-2-yl trifluoromethanesulfonate serves as a valuable tool in modern chemical synthesis, enabling chemists to access diverse molecular structures and functional groups that would be challenging to achieve using conventional methods. Its versatility and efficiency make it a preferred reagent for the synthesis of complex molecules in both academic research and industrial applications.
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GHS Pictogram
Signal Word Danger
UN# 1993
Hazard Statements H226-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class 3
Packing Group

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