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Home> Products> Intermediates> Organic Intermediates> Trifluoromethanesulfonic anhydride CAS 358-23-6
Trifluoromethanesulfonic anhydride CAS 358-23-6
Trifluoromethanesulfonic anhydride CAS 358-23-6
Trifluoromethanesulfonic anhydride CAS 358-23-6
Trifluoromethanesulfonic anhydride CAS 358-23-6
Trifluoromethanesulfonic anhydride CAS 358-23-6
Trifluoromethanesulfonic anhydride CAS 358-23-6

Trifluoromethanesulfonic anhydride CAS 358-23-6

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Payment Type:L/C
Incoterm:FOB
Min. Order:1 Kilogram
Transportation:Land,Ocean,Air,Express
Port:Shanghai Port,Qingdao Port,Ningbo Port
Product Attributes

Model No.vsk 358-23-6

BrandVolksky

Place Of OriginChina

Types OfSyntheses Material Intermediates

Packaging & Delivery
Selling Units : Kilogram
Package Type : 10000 Kilogram/Kilograms per Week
Transparent liquid
Product Description

Trifluoromethanesulfonic anhydride Basic information

    Trifluoromethanesulfonic Anhydride is a strong electrophile used in chemical synthesis for introducing the triflyl group.

Product Name: Trifluoromethanesulfonic anhydride
Synonyms: Trifluoromethanesulfonic anhydlladium(0);Trifluoromethanesulfonic anhydride purum, >=98.0% (T);Trifluoromethanesulfonic anhydride solution 1 M in methylene chloride;Triflic anhydride solution;7561347, DT: 23.1 1.2016) RE-EXPORT;TRIFLUOROMETHANE SULFONIC ANHYDRIDE(ORIG INAL IMPORT VIDE BE.NO;Trifluoromethanesulfonic anhydride solution ;Methanesulfonic acid, trifluoro-, anhydride
CAS: 358-23-6
MF: C2F6O5S2
MW: 282.14
Trifluoromethanesulfonic anhydride Chemical Properties

Melting point  -80°C
Boiling point  81-83 °C (lit.)
density  1.677 g/mL at 25 °C (lit.)
mf Trifluoromethanesulfonic anhydride
Trifluoromethanesulfonic anhydride Usage And Synthesis

    Trifluoromethanesulfonic anhydride is used to convert phenols and imine into triflic ester and NTf group. It is a strong electrophile used for the introduction of triflyl group in chemical synthesis. It serves as a reagent in the preparation of alkyl and vinyl triflates, and for the stereoselective synthesis of mannosazide methyl uronate donors. It acts as a catalyst for glycosylation with anomeric hydroxy sugars to prepare polysaccharides.

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