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inquiryProduct Name: 1H,1H,2H,2H-Perfluorohexan-1-ol Synonyms: 1,1,2,2-Tetrahydroperfluoro-1-hexanol;3,3,4,4,5,5,6,6,6-nonafluoro-1-hexano;1H,1H,2H,2H-NONAFLUORO-1-HEXANOL;1H,1H,2H,2H-NONAFLUOROHEXAN-1-OL;1H,1H,2H,2H-PERFLUOROHEXAN-1-OL;1H,1H
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inquiryProduct Name:1H,1H,2H, 2H-Perfluorohexan-1-ol Cas No:2043-47-2 MF:C6H5F9O MW:264.09 Structural: Appearance: Colorless Liquid Storage:Store in cool and dry place, away from sun light. Package:drum Application:oled Transportation:By sea Por
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inquiry1,1,2,2-Tetrahydroperfluoro-1-hexanol 1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:White Powder Storage:Store
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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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inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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inquiryProName: 1H,1H,2H,2H-Perfluorohexan-1-ol CasNo: 2043-47-2 Molecular Formula: C6H5F9O Appearance: detailed see specifications Application: An important raw material and intermed... DeliveryTime: prompt PackAge: according to the clients require
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inquiryProduct name: Perfluorobutyl Ethanol CAS No.: 2043-47-2 Molecule Formula:C6H5F9O Molecule Weight:264.09 Purity: 99.0% Package: 25kg/drum Description:White powder Manufacture Standards:Enterprise Standard TESTING ITEMS
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inquiryHangzhou Fanda Chemical Co.,Ltd (FandaChem) , a China-based chemical company, specialize in exporting 1H,1H,2H,2H-Perfluorohexan-1-ol CAS:2043-47-2 , Please contact us by email freely. We are leading exporter in China. If you really n
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inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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inquiryConditions | Yield |
---|---|
With hydrogenchloride; formic acid; oxygen; copper; zinc In water at 80℃; for 2h; Product distribution; various solvents, water concentration; | 100% |
With water In N,N-dimethyl-formamide at 125 - 130℃; under 9000.9 Torr; for 30h; Pressure; Solvent; Green chemistry; | 85% |
Yield given. Multistep reaction; | |
With potassium hydroxide In 1-methyl-pyrrolidin-2-one; water; dimethyl sulfoxide at 140℃; under 7125.71 Torr; for 10h; Concentration; Solvent; Temperature; |
potassium 6,6,6,5,5,4,4,3,3-nonafluorohexyl sulfate
1H,1H,2H,2H-nonafluoro-1-hexanol
Conditions | Yield |
---|---|
With hydrogenchloride; water at 70℃; for 25h; pH=0 - 1; | 87% |
3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene
A
1H,1H,2H,2H-nonafluoro-1-hexanol
B
3,3,4,4,5,5,6,6,6-Nonafluoro-2-hexanol
Conditions | Yield |
---|---|
Stage #1: 3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene With bis(cyclohexanyl)borane In tetrahydrofuran at 20℃; for 16h; Stage #2: With dihydrogen peroxide In tetrahydrofuran alkaline solution; Further stages.; |
3-(perfluorohexyl)prop-1-ene
A
1H,1H,2H,2H-nonafluoro-1-hexanol
B
3-(F-hexyl)propan-2-ol
Conditions | Yield |
---|---|
Stage #1: 3-(perfluorohexyl)prop-1-ene With dichloroborane In hexane Stage #2: With dihydrogen peroxide In hexane alkaline solution; Further stages.; |
3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene
A
1H,1H,2H,2H-nonafluoro-1-hexanol
Conditions | Yield |
---|---|
Stage #1: 3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene With benzo[1,3,2]dioxaborole; (η4-cyclooctadiene)((R)-2,2'-bis(diphenylphosphanyl)-1,1'-binaphthyl)rhodium(I) tetrfluoroborate In tetrahydrofuran at 0℃; for 1h; Stage #2: With sodium hydroxide; dihydrogen peroxide In ethanol Further stages. Title compound not separated from byproducts.; |
3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane
A
1H,1H,2H,2H-nonafluoro-1-hexanol
B
3,3,4,4,5,5,6,6,6-Nonafluoro-2-hexanol
Conditions | Yield |
---|---|
Stage #1: 3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane; Wilkinson's catalyst In tetrahydrofuran at 20℃; for 2.5h; Stage #2: With sodium hydroxide; dihydrogen peroxide In tetrahydrofuran Further stages. Title compound not separated from byproducts.; |
3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene
benzo[1,3,2]dioxaborole
A
1H,1H,2H,2H-nonafluoro-1-hexanol
B
3,3,4,4,5,5,6,6,6-Nonafluoro-2-hexanol
Conditions | Yield |
---|---|
Stage #1: 3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene; benzo[1,3,2]dioxaborole; Wilkinson's catalyst In tetrahydrofuran at 20℃; for 1h; Stage #2: With sodium hydroxide; dihydrogen peroxide In tetrahydrofuran Further stages. Title compound not separated from byproducts.; |
3,3,4,4,5,5,6,6,6-nonafluorohexyliodide
1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane
2-(n-perfluorooctyl)ethyl iodide
1-iodo-1H,1H,2H,2H-perfluorododecane
1-iodo-1H,1H,2H,2H-perfluorotetradecane
A
1H,1H,2H,2H-perfluorohexadecan-1-ol
B
1H,1H,2H,2H-tridecafluoro-n-octanol
C
2-(perfluorodecyl)ethanol
D
1H,1H,2H,2H-nonafluoro-1-hexanol
E
1H,1H,2H,2H-perfluorobutadecan-1-ol
F
3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-decanol
Conditions | Yield |
---|---|
With water; silver nitrate; copper(II) sulfate at 180℃; Conversion of starting material; Gas phase; |
3,3,4,4,5,5,6,6,6-nonafluorohexyliodide
potassium acrylate
A
perfluorobutylethyl acrylate
B
3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene
C
1H,1H,2H,2H-nonafluoro-1-hexanol
Conditions | Yield |
---|---|
With 10H-phenothiazine In tert-butyl alcohol at 160℃; for 6h; |
1H,1H,2H,2H-nonafluoro-1-hexanol
3,3,4,4,5,5,6,6,6-nonafluorohexanoic acid
Conditions | Yield |
---|---|
With chromium(VI) oxide; sulfuric acid In diethyl ether; acetone for 0.0833333h; | 98% |
With chromium(VI) oxide; sulfuric acid In diethyl ether; water; acetone for 0.5h; Jones oxidation; | 81% |
With Jones reagent In diethyl ether; acetone |
1H,1H,2H,2H-nonafluoro-1-hexanol
Conditions | Yield |
---|---|
With tetraphosphorus decasulfide In toluene Heating; | 98% |
ethyl bromide
1H,1H,2H,2H-nonafluoro-1-hexanol
1,1,1,2,2,3,3,4,4-nonafluoro-7-oxanonane
Conditions | Yield |
---|---|
With potassium hydroxide In 1-methyl-pyrrolidin-2-one; water at 50 - 70℃; for 7h; | 95% |
Conditions | Yield |
---|---|
With (4,4′-di-tert-butyl-2,2′-dipyridyl)Ni(o-tolyl)(Br); 1,8-diazabicyclo[5.4.0]undec-7-ene In toluene at 80℃; for 12h; Inert atmosphere; Sealed tube; UV-irradiation; | 95% |
1H,1H,2H,2H-nonafluoro-1-hexanol
p-toluenesulfonyl chloride
toluene-4-sulfonic acid 3,3,4,4,5,5,6,6,6-nonafluorohexyl ester
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane at 0℃; for 3h; Inert atmosphere; | 94% |
With dmap; triethylamine |
1H,1H,2H,2H-nonafluoro-1-hexanol
acrylic acid
perfluorobutylethyl acrylate
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid; hydroquinone at 80℃; for 5.5h; Reagent/catalyst; Green chemistry; | 92.2% |
Stage #1: 1H,1H,2H,2H-nonafluoro-1-hexanol; acrylic acid With sodium carbonate; triethylamine; benzenesulfonyl chloride; Sumilizer GM In dichloromethane at 30 - 40℃; for 2h; Stage #2: With water In dichloromethane for 1h; Stage #3: acrylic acid With water; triethylamine; benzenesulfonyl chloride Product distribution / selectivity; more than 3 stages; | 84% |
Stage #1: 1H,1H,2H,2H-nonafluoro-1-hexanol; acrylic acid With triethylamine; benzenesulfonyl chloride; Sumilizer GM In dichloromethane at 20 - 40℃; for 3h; Stage #2: With water In dichloromethane for 0.5h; Product distribution / selectivity; | 76% |
1H,1H,2H,2H-nonafluoro-1-hexanol
4'-(Benzyloxy)-biphenyl-4-carboxylic acid
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; | 92% |
1H,1H,2H,2H-nonafluoro-1-hexanol
1H,1H,2H,2H-perfluorohexyl trifluoromethanesulfonate
Conditions | Yield |
---|---|
With trifluoromethylsulfonic anhydride; triethylamine In dichloromethane at 5℃; for 24h; | 91.8% |
1H,1H,2H,2H-nonafluoro-1-hexanol
Conditions | Yield |
---|---|
Stage #1: 1H,1H,2H,2H-nonafluoro-1-hexanol With pyridine; di(succinimido) carbonate In N,N-dimethyl-formamide at 40℃; for 15h; Stage #2: Nα-(tert-butyloxycarbonyl)-(R)-lysine tert-butyl ester In N,N-dimethyl-formamide at 20 - 30℃; | 91% |
1H,1H,2H,2H-nonafluoro-1-hexanol
A
3,3,4,4,5,5,6,6,6-nonafluorohexyl 2,2-difluoro-3-hydroxy-4-methylpentanoate
B
3,3,4,4,5,5,6,6,6-nonafluorohexyl 2,2-difluoro-3-methacryloyloxy-4-methylpentanoate
Conditions | Yield |
---|---|
A 87% B n/a | |
A 87% B n/a |
1H,1H,2H,2H-nonafluoro-1-hexanol
propyl bromide
1,1,1,2,2,3,3,4,4-nonafluoro-7-oxadecane
Conditions | Yield |
---|---|
Stage #1: 1H,1H,2H,2H-nonafluoro-1-hexanol With sodium hydroxide In tetrahydrofuran; cyclohexane; water at 25℃; for 2h; Stage #2: propyl bromide; N-benzyl-N,N,N-triethylammonium chloride In tetrahydrofuran; cyclohexane; water at 40 - 70℃; for 48h; | 86% |
With potassium hydroxide In 1-methyl-pyrrolidin-2-one; water at 50 - 70℃; for 7h; | 84% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid at 140℃; for 8h; | 85% |
With toluene-4-sulfonic acid In toluene at 20℃; Reflux; | 80% |
With toluene-4-sulfonic acid In toluene at 20℃; Reflux; | 80% |
With toluene-4-sulfonic acid In toluene at 110℃; for 15h; | 61.5% |
1-Bromopentane
1H,1H,2H,2H-nonafluoro-1-hexanol
1,1,1,2,2,3,3,4,4-nonafluoro-7-oxadodecane
Conditions | Yield |
---|---|
With potassium hydroxide In 1-methyl-pyrrolidin-2-one; water at 50 - 70℃; for 7h; | 83% |
Stage #1: 1H,1H,2H,2H-nonafluoro-1-hexanol With sodium hydroxide In tetrahydrofuran; cyclohexane; water at 25℃; for 2h; Stage #2: 1-Bromopentane; N-benzyl-N,N,N-triethylammonium chloride In tetrahydrofuran; cyclohexane; water at 40 - 70℃; for 48h; | 79% |
methacryloyl anhydride
1H,1H,2H,2H-nonafluoro-1-hexanol
3,3,4,4,5,5,6,6,6,-nonafluorohexyl methacrylate
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane; 1,1,2-Trichloro-1,2,2-trifluoroethane at 30℃; for 18h; | 80% |
Conditions | Yield |
---|---|
With (4,4′-di-tert-butyl-2,2′-dipyridyl)Ni(o-tolyl)(Br); 1,8-diazabicyclo[5.4.0]undec-7-ene In toluene at 80℃; for 12h; Inert atmosphere; Sealed tube; UV-irradiation; | 78% |
1H,1H,2H,2H-nonafluoro-1-hexanol
allyl bromide
6-(allyloxy)-1,1,1,2,2,3,3,4,4-nonafluorohexane
Conditions | Yield |
---|---|
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate at 65℃; for 16h; | 76% |
Stage #1: 1H,1H,2H,2H-nonafluoro-1-hexanol With tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide for 0.333333h; Stage #2: allyl bromide at 65℃; for 14h; | 76% |
With sodium hydroxide; tetrabutylammomium bromide In tetrahydrofuran for 5h; Heating / reflux; |
Conditions | Yield |
---|---|
With sodium hydroxide In tetrahydrofuran; water at 50℃; for 24h; | 74% |
Stage #1: 1H,1H,2H,2H-nonafluoro-1-hexanol With sodium hydroxide In N,N-dimethyl-formamide at -15℃; for 0.166667h; Stage #2: propargyl bromide In N,N-dimethyl-formamide at -15 - 20℃; for 24h; | 71% |
1H,1H,2H,2H-nonafluoro-1-hexanol
Conditions | Yield |
---|---|
With tert-butyl alcohol; phosphorus trichloride In dichloromethane for 15h; | 73% |
Conditions | Yield |
---|---|
Stage #1: 1H,1H,2H,2H-nonafluoro-1-hexanol With sodium hydride In tetrahydrofuran at 0℃; for 0.583333h; Inert atmosphere; Stage #2: phenyl isothiocyanate In tetrahydrofuran at 0 - 20℃; for 3h; Inert atmosphere; | 73% |
1-Bromotetradecane
1H,1H,2H,2H-nonafluoro-1-hexanol
1,1,1,2,2,3,3,4,4-nonafluoro-7-oxaheneicosane
Conditions | Yield |
---|---|
With potassium hydroxide In 1-methyl-pyrrolidin-2-one; water at 50 - 70℃; for 7h; | 71% |
1-bromo-octane
1H,1H,2H,2H-nonafluoro-1-hexanol
1,1,1,2,2,3,3,4,4-nonafluoro-7-oxapentadecane
Conditions | Yield |
---|---|
With potassium hydroxide In 1-methyl-pyrrolidin-2-one; water at 50 - 70℃; for 7h; | 70% |
Conditions | Yield |
---|---|
Stage #1: 1H,1H,2H,2H-nonafluoro-1-hexanol With sodium hydride In tetrahydrofuran at 0℃; for 0.583333h; Inert atmosphere; Stage #2: Benzyl isothiocyanate In tetrahydrofuran at 0 - 20℃; for 3h; Inert atmosphere; | 70% |
1H,1H,2H,2H-nonafluoro-1-hexanol
2-Bromoacetyl bromide
2-Perfluorobutylethyl-α-bromoacetate
Conditions | Yield |
---|---|
In diethyl ether at 60℃; for 12h; | 69% |
Heneicosyl bromide
1H,1H,2H,2H-nonafluoro-1-hexanol
1,1,1,2,2,3,3,4,4-nonafluoro-7-oxaoctacosane
Conditions | Yield |
---|---|
With potassium hydroxide In 1-methyl-pyrrolidin-2-one; water at 50 - 70℃; for 7h; | 69% |
Conditions | Yield |
---|---|
Stage #1: 1H,1H,2H,2H-nonafluoro-1-hexanol With sodium hydride In tetrahydrofuran at 0℃; for 0.583333h; Inert atmosphere; Stage #2: Ethyl isothiocyanate In tetrahydrofuran at 0 - 20℃; for 3h; Inert atmosphere; | 66% |
1H,1H,2H,2H-nonafluoro-1-hexanol
2-(2,2,3,3,4,4,5,5,6,6,6-Undecafluoro-hexanoyl)-cyclopentanone
7,7,8,8,9,9,10,10,11,11,11-Undecafluoro-6-oxo-undecanoic acid 3,3,4,4,5,5,6,6,6-nonafluoro-hexyl ester
Conditions | Yield |
---|---|
at 70℃; for 120h; | 65% |
1H,1H,2H,2H-nonafluoro-1-hexanol
1-Bromooctadecane
1,1,1,2,2,3,3,4,4-nonafluoro-7-oxapentacosane,
Conditions | Yield |
---|---|
With potassium hydroxide In 1-methyl-pyrrolidin-2-one; water at 50 - 70℃; for 7h; | 65% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene for 48h; Reflux; Dean-Stark; | 65% |
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