We have been specializing in organic fluoro chemicals since 1984. We have been supplying it to Europe, USA, Japan, Korea etc. regularly for several years Superiority 1.Powerful R & D team 2.The ability of quantized production,from gram
Cas:33454-82-9
Min.Order:100 Gram
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Type:Lab/Research institutions
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Min.Order:1 Metric Ton
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Type:Manufacturers
inquiryhebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm
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Min.Order:1 Metric Ton
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inquiryBottom price high quality Lithium triflate Cas 33454-82-9 with reliable factory Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its intermediates,
Cas:33454-82-9
Min.Order:10 Kilogram
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Type:Trading Company
inquiryProduct description: Product name Lithium trifluoromethanesulfonate CAS number 33454-82-9 Assay ≥99% Appearance White powder Capacity 500mt/year Application Plant growth regu
Cas:33454-82-9
Min.Order:10 Gram
FOB Price: $12.0
Type:Lab/Research institutions
inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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inquiryhigh purity Storage:Sealed, dry, microtherm , avoid light and smell. Package:meet customer's demand Application:organic synthesis Transportation:by sea or by air Port:shanghai
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Cas:33454-82-9
Min.Order:1 Gram
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Type:Manufacturers
inquiryTrifluoromethanesulfonic acid lithium salt Manufacturer CAS no 33454-82-9 Chemwill Asia co.,Ltd is one of the leading manufacturer in CHINA.We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.O
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inquiryProduct Name: Lithium triflate Synonyms: Methanesulfonicacid,trifluoro-,lithiumsalt;trifluoro-methanesulfonicacilithiumsalt;Lithium triflate, Trifluoromethanesulfonic acid lithium salt;Lithium trifluoromethanesulfonate ,97%;Lithium tri
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Type:Lab/Research institutions
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Min.Order:1 Kilogram
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inquiryProduct name Lithium triflate CAS 33454-82-9 Name Lithium trifluoromethanesulfonate Color White Powder Boiling Point 162°Cat760mmHg
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Type:Trading Company
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Cas:33454-82-9
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Min.Order:1 Gram
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Type:Lab/Research institutions
inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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Type:Lab/Research institutions
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Min.Order:1 Kilogram
Negotiable
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Min.Order:1 Kilogram
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Min.Order:1 Gram
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Negotiable
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inquiryBuy High quality 33454-82-9 low price Lithium triflate on hot selling the conductivity and electrochemical stability of lithium trifluoromethanesulfonate are not as good as LiPF6, but its thermal stability, water absorption decomposition and cycle p
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Min.Order:1 Gram
Negotiable
Type:Other
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inquirytrifluorormethanesulfonic acid
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In water at 100℃; for 1h; | 93.3% |
LiSn(C6H5)2CH3
{(CH3)3C}{(CH3)2CH}Si(OSO2CF3)2
trifluorormethanesulfonic acid
dimethyl amine
A
{(CH3)3C}{(CH3)2CH}{(CH3)2N}SiSn{N(CH3)2}(C6H5)CH3
B
lithium trifluoromethanesulfonate
C
[Me2NH2]OTf
Conditions | Yield |
---|---|
In diethyl ether; toluene byproducts: C6H6; Ar-atmosphere; addn. of LiSnPh2Me to Si-derivative in ether (-&0°C), toluene addn., addn. of triflic acid (-70°C), stirring (3 h, -70°C), addn. of Me2NH (-40°C); sepn. of Me2NH2OSO2CF3, filtration, evapn. (vac.), fractional distn.; mixt. of stereoisomers (1 : 1) not sepd.; elem. anal.; | A 54% B n/a C n/a |
barium trifluoromethanesulfonate
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
With lithium sulfate In water for 24h; |
bis(trifluoromethyl)sulfone
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
With lithium hydroxide In methanol at 0℃; for 0.5h; |
barium trifluoromethanesulfonate
lithium hydroxide
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
With sulfuric acid In water | |
With dild. H2SO4 In water |
trifluorormethanesulfonic acid
lithium hydroxide
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
byproducts: H2O; |
Trifluoromethanesulfonyl fluoride
lithium hydroxide
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
byproducts: HF; |
Lithium enolate of the acetaldehyde
copper(II) bis(trifluoromethanesulfonate)
lithium trifluoromethanesulfonate
copper(II) bis(trifluoromethanesulfonate)
1,2,2-triphenyl-ethanone; lithium enolate
lithium trifluoromethanesulfonate
(C6H5)2Sn(OSO2CF3)2
lithium hexamethyldisilazane
A
(C6H5)2Sn{N(Si(CH3)3)2}(OSO2CF3)
B
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In diethyl ether Ar-atmosphere; mixing at -50°C, warming to room temp. (during 2 h); evapn. (vac., room temp.), toluene addn. filtration off of Li-triflate, evapn. (vac.); elem. anal.; | A >95 B n/a |
(C6H5)2Sn(OSO2CF3)2
lithium phenylacetylide
A
(C6H5)2Sn(CCC6H5)OSO2CF3
B
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In diethyl ether Ar-atmosphere; mixing at -50°C, warming to room temp. (during 2 h); evapn. (vac., room temp.), toluene addn. filtration off of Li-triflate, evapn. (vac.); elem. anal.; | A >95 B n/a |
bis(trifluoromethanesulfonyloxy)dimethylsilane
triphenylgermyl lithium
A
(CH3)2SiGe(C6H5)3(OSO2CF3)
B
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In diethyl ether Ar-atmosphere; mixing at -70°C, stirring and warming to 0°C (3 h); evapn. (vac., 0°C), toluene addn., filtration off of Li-triflate (cooling), evapn. (vac.); elem. anal.; | A >95 B n/a |
bis(trifluoromethanesulfonyloxy)dimethylsilane
lithium triphenylstannide
A
(CH3)2SiSn(C6H5)3(OSO2CF3)
B
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In diethyl ether Ar-atmosphere; mixing at -70°C, stirring and warming to 0°C (3 h); evapn. (vac., 0°C), toluene addn., filtration off of Li-triflate (cooling), evapn. (vac.); elem. anal.; | A >95 B n/a |
(C6H5)2Sn(OSO2CF3)2
lithium diphenylphosphide
A
(C6H5)2Sn{P(C6H5)2}(OSO2CF3)
B
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In diethyl ether Ar-atmosphere; mixing at -50°C, warming to room temp. (during 2 h); evapn. (vac., room temp.), toluene addn. filtration off of Li-triflate, evapn. (vac.); elem. anal.; | A >95 B n/a |
Trifluoromethanesulfonyl fluoride
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
With calcium oxide; lithium hydroxide In water for 9.5h; | 1001 g |
lithium trifluoromethanesulfonate
(4'-formyl-1,1'-biphenyl-4-yl)(triphenyl)phosphonium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In dichloromethane; water; acetonitrile for 1h; | 100% |
bis(4-fluorophenyl)sulfoxide
lithium trifluoromethanesulfonate
10H-acridin-9-one
CF3O3S(1-)*C25H16F2NOS(1+)
Conditions | Yield |
---|---|
Stage #1: bis(4-fluorophenyl)sulfoxide; 10H-acridin-9-one With methanesulfonic acid; phosphorus pentoxide In chlorobenzene at 50℃; for 2h; Inert atmosphere; Stage #2: lithium trifluoromethanesulfonate In dichloromethane for 1h; | 100% |
lithium trifluoromethanesulfonate
C26H43F3LiNO8S
Conditions | Yield |
---|---|
In diethyl ether at 20℃; Inert atmosphere; Schlenk technique; | 100% |
Tetraethylene glycol dimethyl ether
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
at 79.84℃; for 0.5h; | 100% |
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
With fluorine In acetonitrile at -10 - 20℃; Inert atmosphere; | 99% |
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In chloroform at 20℃; for 0.5h; | 99% |
Conditions | Yield |
---|---|
In ethanol at 80℃; for 0.333333h; Irradiation; | 99% |
Conditions | Yield |
---|---|
In water at 20℃; for 2h; | 99% |
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In water at 20℃; for 24h; | 99% |
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In ethanol; water at 20℃; for 4h; | 98.6% |
1-(1-methyl-1-pyrrolidinio)propane-3-sulfonate
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In methanol for 12h; | 98% |
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In dichloromethane for 8h; Inert atmosphere; | 98% |
In dichloromethane | 92% |
lithium trifluoromethanesulfonate
acrolein
Conditions | Yield |
---|---|
In acetonitrile N2; org. compd. dissoln. in CH3CN containing Li-salt, this soln. addn. to Os-compd., soln. stirring for ca. 12 h, pptn. on adding to stirring Et2O; ppt. filtration off, rinsing (ether), vac. drying; elem. anal.; | 97% |
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In dichloromethane for 0.166667h; Glovebox; Inert atmosphere; | 97% |
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In methanol at 20℃; for 12h; | 97% |
lithium trifluoromethanesulfonate
trifluorormethanesulfonic acid
Conditions | Yield |
---|---|
With sulfuric acid | 96.8% |
methyl (4-pyridyl) ketone
lithium trifluoromethanesulfonate
N-Fluoro-4-acetylpyridinium triflate
Conditions | Yield |
---|---|
With fluorine In acetonitrile at -40℃; for 3h; | 96% |
lithium trifluoromethanesulfonate
1-butyl-3-methylimidazolium chloride
1-(n-butyl)-3-methylimidazolium triflate
Conditions | Yield |
---|---|
In water | 96% |
In dichloromethane at 20℃; for 72h; Inert atmosphere; | 86.7% |
In acetonitrile Heating; | 82.8% |
4-(1-methylpyrrolidinium-1-yl)butane-1-sulfonate
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In methanol for 12h; | 96% |
4-aza-1-benzylazoniabicyclo<2.2.2>octane chloride
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 24h; Inert atmosphere; | 96% |
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
Stage #1: 1,1'-(pyridine-2,6-diyl)bis(3-(4-(phenylethynyl)benzyl)-1H-benzo[d]imidazol-3-ium) dibromide; lithium trifluoromethanesulfonate In methanol; acetonitrile at 85℃; for 12h; Stage #2: In water at 100℃; for 12h; | 96% |
Br(1-)*C23H39N2(1+)
lithium trifluoromethanesulfonate
CF3O3S(1-)*C23H39N2(1+)
Conditions | Yield |
---|---|
In water for 1h; | 95% |
Conditions | Yield |
---|---|
In methanol at 20℃; for 12h; | 95% |
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In methanol at 20℃; for 12h; | 95% |
Conditions | Yield |
---|---|
In acetonitrile at 50 - 60℃; for 5h; | 95% |
pyridine-4-carbonitrile
lithium trifluoromethanesulfonate
N-Fluoro-4-cyanopyridinium triflate
Conditions | Yield |
---|---|
With fluorine In acetonitrile at -40℃; for 3h; | 94% |
((2,6-bis(1-methylbenzimidazole-2-yl)pyridine)(Cl)Ru)2Cl2
lithium trifluoromethanesulfonate
acetylacetone
Conditions | Yield |
---|---|
Stage #1: ((2,6-bis(1-methylbenzimidazole-2-yl)pyridine)(Cl)Ru)2Cl2 With trifluorormethanesulfonic acid for 1h; Stage #2: acetylacetone With triethylamine In methanol for 3h; Inert atmosphere; Reflux; Stage #3: lithium trifluoromethanesulfonate In water | 94% |
Conditions | Yield |
---|---|
In water at 20℃; for 2h; | 94% |
lithium trifluoromethanesulfonate
Conditions | Yield |
---|---|
Stage #1: C19H34N4(2+)*2Br(1-); C14H13ClN2Pt With triethylamine In acetonitrile at 90℃; for 24h; Stage #2: lithium trifluoromethanesulfonate In acetonitrile at 20℃; | 94% |
lithium trifluoromethanesulfonate
n-decyl-tri-n-butylphosphonium bromide
Conditions | Yield |
---|---|
In water; acetone at 20℃; for 15h; | 93.4% |
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