What is the Sodium trifluoromethanesulfonate?

Sodium trifluoromethanesulfonate is White to off-white powder, while it's Molecular Formula is CF3HSO3Na. White to off-white powder Sodium trifluoromethanesulfonate can be employed as a reagent for the preparation of: Aryl fluorides via silver-catalyzed fluorination of arylstannanes.Ionic liquids such as N, N -dialkylpyrrolidinium triflate, N,N-dialkylimidazolium triflate, and N-alkylpyridinium triflate.It can be also used as supporting electrolyte in electrochemical O-glycosylation of primary alcohols with O-protected thioglycosides.

What is the CAS number for Sodium trifluoromethanesulfonate?

The CAS number of Sodium trifluoromethanesulfonate is 2926-30-9.

What is Sodium trifluoromethanesulfonate (2926-30-9) used for?

Sodium trifluoromethanesulfonate, also known as Sodium triflate or NaOTf, is a white to off-white powder that serves as an efficient catalyst and reagent in various organic reactions. It is particularly prominent in catalytic asymmetric Mannich-type reactions, Mannich-type reactions in water, and Diels-Alder reactions.InChI:InChI=1/CHF3O3S.Na/c2-1(3,4)8(5,6)7;/h(H,5,6,7);/q;+1/p-1

What is the Sodium trifluoromethanesulfonate?

Sodium trifluoromethanesulfonate is White to off-white powder, while it's Molecular Formula is CF3HSO3Na. White to off-white powder Sodium trifluoromethanesulfonate can be employed as a reagent for the preparation of: Aryl fluorides via silver-catalyzed fluorination of arylstannanes.Ionic liquids such as N, N -dialkylpyrrolidinium triflate, N,N-dialkylimidazolium triflate, and N-alkylpyridinium triflate.It can be also used as supporting electrolyte in electrochemical O-glycosylation of primary alcohols with O-protected thioglycosides.

What is the CAS number for Sodium trifluoromethanesulfonate?

The CAS number of Sodium trifluoromethanesulfonate is 2926-30-9.

What is Sodium trifluoromethanesulfonate (2926-30-9) used for?

Sodium trifluoromethanesulfonate, also known as Sodium triflate or NaOTf, is a white to off-white powder that serves as an efficient catalyst and reagent in various organic reactions. It is particularly prominent in catalytic asymmetric Mannich-type reactions, Mannich-type reactions in water, and Diels-Alder reactions.InChI:InChI=1/CHF3O3S.Na/c2-1(3,4)8(5,6)7;/h(H,5,6,7);/q;+1/p-1

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Sodium trifluoromethanesulfonate

CAS
Purity

2926-30-9
99%

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Bulk supply high purity Sodium trifluoromethanesulfonate 2926-30-9, Paid sample available

Molecular Formula: CF3HSO3Na
Molecular Weight: 172.06
Appearance/Colour: White to off-white powder
Vapor Pressure: 1.14mmHg at 25°C
Melting Point: 253-255 °C(lit.)
Boiling Point: 162 °C at 760 mmHg
PSA： 65.58000
LogP: 1.13220

Sodium trifluoromethanesulfonate(Cas 2926-30-9) Usage

General Description

Sodium trifluoromethanesulfonate (Sodium triflate or NaOTf) is an efficient catalyst as well as a reagent in many organic reactions. The prominent application includes catalytic asymmetric Mannich-type reactions, Mannich-type reactions in water, and Diels-Alder reactions.

InChI:InChI=1/CHF3O3S.Na/c2-1(3,4)8(5,6)7;/h(H,5,6,7);/q;+1/p-1

2926-30-9 Relevant articles

Preparation method of trifluoromethane sulfonic acid

-

Paragraph 0028; 0031, (2017/01/09)

The invention relates to a preparation m...

Catalytic enantioselective carboannulation with allylsilanes

Ball-Jones, Nicolas R.,Badillo, Joseph J.,Tran, Ngon T.,Franz, Annaliese K.

supporting information, p. 9462 - 9465 (2015/02/05)

The first catalytic asymmetric carboannu...

Two different hydrogen bond donor ligands together: A selectivity improvement in organometallic {Re(CO)3} anion hosts

Ion, Laura,Nieto, Sonia,Perez, Julio,Riera, Lucia,Riera, Victor,Diaz, Jesus,Lopez, Ramon,Anderson, Kirsty M.,Steed, Jonathan W.

, p. 8524 - 8531 (2011/10/12)

Rhenium(I) compounds [Re(CO)3(Hdmpz)2(am...

Method for preparing sulphonate salts

-

, (2008/06/13)

The invention concerns a method for prep...

2926-30-9 Process route

: 84370-17-2
Trifluoro-methanesulfonate((Z)-1-butyl-2-trifluoromethanesulfonyloxy-hex-1-enyl)-triphenyl-phosphonium;

: 1942-46-7
5-decyne

: 2926-30-9
sodium triflate

: 603-35-0
triphenylphosphine

Conditions

Conditions	Yield
With sodium amalgam; In tetrahydrofuran; at 5 ℃; for 17h;	45%

: 64-17-5
ethanol

: 335-05-7
Trifluoromethanesulfonyl fluoride

: 425-75-2
trifluoromethanesulfonic acid ethyl ester

: 2926-30-9
sodium triflate

Conditions

Conditions	Yield
100°C, 1 h, absolute ethanol;	0%
100°C, 1 h, absolute ethanol;	0%

2926-30-9 Upstream products

2926-29-6
Langlois reagent
2794-60-7
barium trifluoromethanesulfonate
84370-15-0
Trifluoro-methanesulfonate((Z)-1-methyl-2-phenyl-2-trifluoromethanesulfonyloxy-vinyl)-triphenyl-phosphonium;
84370-17-2
Trifluoro-methanesulfonate((Z)-1-butyl-2-trifluoromethanesulfonyloxy-hex-1-enyl)-triphenyl-phosphonium;