82113-65-3

  • Product Name:Trifluoromethanesulfonimide
  • MF:C2HF6NO4S2
  • Purity:99%
  • Molecular Weight:281.157
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Product Details

Cost-effective and customizable Trifluoromethanesulfonimide 82113-65-3 supplier

  • Molecular Formula:C2HF6NO4S2
  • Molecular Weight:281.157
  • Appearance/Colour:light yellow to brown liquid 
  • Vapor Pressure:0.274mmHg at 25°C 
  • Melting Point:52-56 °C 
  • Refractive Index:1.523 
  • Boiling Point:190.5 °C at 760 mmHg 
  • PKA:-10.42±0.40(Predicted) 
  • Flash Point:69 °C 
  • PSA:97.07000 
  • Density:1.936 g/cm3 
  • LogP:2.82770 

TRIFLUOROMETHANESULFONIMIDE(Cas 82113-65-3) Usage

General Description

Bis(trifluoromethane)sulfonimide (TFSI, Tf2N) is utilized as anion species to form 1-ethyl-3-methylimidazolium molten salts. It undergoes acid-base complexation with rod-like poly(2,5-pyridine) to afford highly-ordered lamellar self-assemblies in the hydrated films.

InChI:InChI=1/C8H7F3OS/c9-8(10,11)13-7-3-1-2-6(4-7)5-12/h1-4,12H,5H2

82113-65-3 Relevant articles

Thermally stable bis(trifluoromethylsulfonyl)imide salts and their mixtures

Scheuermeyer, Marlene,Kusche, Matthias,Agel, Friederike,Schreiber, Patrick,Maier, Florian,Steinrück, Hans-Peter,Davis, James H.,Heym, Florian,Jess, Andreas,Wasserscheid, Peter

, p. 7157 - 7161 (2016)

We show that both tetraphenylphosphonium...

N-FLUORO-BIS(TRIFLUOROMETHANESULFONYL)IMIDE AN IMPROVED SYNTHESIS

Desmarteau, Darryl D.,Witz, Michael

, p. 7 - 12 (1991)

An improved synthesis of (CF3SO2)2NH and...

A one-pot synthesis of a ternary nanocomposite based on mesoporous silica, polyaniline and silver

Rosa, Ana Claudia De Abreu,Correa, Cintia Marques,Faez, Roselena,Bizeto, Marcos Augusto,Camilo, Fernanda Ferraz

, p. 26142 - 26148 (2013)

The research on hybrid materials compose...

PERFLUOROALKYL SULFONAMIDE AND METHOD FOR PRODUCING THE SAME

-

Paragraph 0070-0074, (2018/06/05)

PROBLEM TO BE SOLVED: To simply provide ...

Silylium-Catalyzed Carbon–Carbon Coupling of Alkynylsilanes with (2-Bromo-1-methoxyethyl)arenes: Alternative Approaches

Rubial, Belén,Ballesteros, Alfredo,González, José M.

supporting information, p. 6194 - 6198 (2018/07/31)

The catalytic activation of alkynylsilan...

Preparation method of LiN(CF3SO2)2 salt

-

Paragraph 0044; 0046; 0049; 0052; 0054, (2018/02/04)

The invention discloses a preparation me...

METHOD FOR PRODUCING TRIFLUOROMETHANESULFONYL IMIDE OR ITS SALT

-

Paragraph 0154; 0155, (2017/02/28)

The present invention relates to trifluo...

82113-65-3 Process route

(CH<sub>3</sub>)3CN(SO<sub>2</sub>CF<sub>3</sub>)2
41804-81-3

(CH3)3CN(SO2CF3)2

bis(trifluoromethanesulfonyl)amide
82113-65-3

bis(trifluoromethanesulfonyl)amide

isobutene
115-11-7,15220-85-6

isobutene

Conditions
Conditions Yield
decompn. with quantitative elimination of (CH3)2CH2;
>99
decompn. with quantitative elimination of (CH3)2CH2;
>99
trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

trifluorormethanesulfonic acid
1493-13-6

trifluorormethanesulfonic acid

bis(trifluoromethanesulfonyl)amide
82113-65-3

bis(trifluoromethanesulfonyl)amide

Conditions
Conditions Yield
trifluoromethane sulfonyl chloride; With dmap; ammonia; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃;
With dihydrogen peroxide; In water; at 80 ℃;

82113-65-3 Upstream products

  • 91742-21-1
    91742-21-1

    sodium bis(trifluoromethanesulfonyl)imide

  • 91742-20-0
    91742-20-0

    N-(trimethylsilyl)trifluoromethanesulfonamide N-sodium salt

  • 90076-65-6
    90076-65-6

    bis(trifluoromethane)sulfonimide lithium

  • 41804-81-3
    41804-81-3

    (CH3)3CN(SO2CF3)2

82113-65-3 Downstream products

  • 149108-74-7
    149108-74-7

    5-trifluoromethanesulfonyloxy-3,4-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester

  • 180691-65-0
    180691-65-0

    5-trifluoromethanesulfonyloxy-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester

  • 187737-37-7
    187737-37-7

    propene

  • 82113-66-4
    82113-66-4

    trimethylsilyl bis(trifluoromethanesulfonyl)imide