2043-47-2
- Product Name：2-Perfluorobutyl ethyl alcohol
- Molecular Formula：C6H5 F9 O
- Purity：99%
- Molecular Weight：264.091
Product Details;
CasNo： 2043-47-2
Molecular Formula： C6H5 F9 O
factory and supplier 2043-47-2 2-Perfluorobutyl ethyl alcohol in stock
- Molecular Formula:C6H5 F9 O
- Molecular Weight:264.091
- Vapor Pressure:12.9mmHg at 25°C
- Refractive Index:n20/D 1.314(lit.)
- Boiling Point:140-143 ºC
- PKA:14.16±0.10(Predicted)
- Flash Point:164 ºF
- PSA：20.23000
- Density:1.59
- LogP:2.83700
1H,1H,2H,2H-Perfluorohexan-1-ol(Cas 2043-47-2) Usage
InChI:InChI=1/C6H5F9O/c7-3(8,1-2-16)4(9,10)5(11,12)6(13,14)15/h16H,1-2H2
2043-47-2 Relevant articles
New insights on the asymmetric hydroboration of perfluoroalkenes
Segarra, Anna M.,Claver, Carmen,Fernandez, Elena
, p. 464 - 465 (2004)
Enantioselective access to Markovnikov r...
-
Blancou,H.,Benefice,S.
, p. 57 (1983)
-
Environmentally friendly preparation method of fluorine-containing acrylate
-
Paragraph 0019; 0022; 0029; 0032, (2019/01/06)
The invention relates to the technical f...
Method for preparing perfluoroalkyl ethanol
-
Paragraph 0026-0032, (2017/11/29)
The invention discloses a method for pre...
Synthesis of 2-(perfluoroalkyl)ethyl potassium sulfates based on perfluorinated Grignard reagents
Paterová, Jana,Skalicky, Martin,Rybá?ková, Markéta,Kví?alová, Magdalena,Cva?ka, Josef,Kví?ala, Jaroslav
experimental part, p. 1338 - 1343 (2011/02/22)
The first example of nucleophilic substi...
Purification of fluorinated alcohols
-
Page/Page column 4-5, (2008/06/13)
A process for reducing the level of perf...
2043-47-2 Process route
-
-
2043-55-2,71215-70-8
3,3,4,4,5,5,6,6,6-nonafluorohexyliodide
-
-
2043-47-2
1H,1H,2H,2H-nonafluoro-1-hexanol
| Conditions | 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 ℃;
for 30h;
under 9000.9 Torr;
Pressure;
Solvent;
Green chemistry;
|
85% |
|
Yield given. Multistep reaction;
|
|
|
With
potassium hydroxide;
In
1-methyl-pyrrolidin-2-one; water; dimethyl sulfoxide;
at 140 ℃;
for 10h;
under 7125.71 Torr;
Concentration;
Solvent;
Temperature;
|
-
-
2043-55-2,71215-70-8
3,3,4,4,5,5,6,6,6-nonafluorohexyliodide
-
-
10192-85-5
potassium acrylate
-
-
52591-27-2
perfluorobutylethyl acrylate
-
-
19430-93-4
3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene
-
-
2043-47-2
1H,1H,2H,2H-nonafluoro-1-hexanol
| Conditions | Yield |
|---|---|
|
With
10H-phenothiazine;
In
tert-butyl alcohol;
at 160 ℃;
for 6h;
|
2043-47-2 Upstream products
-
2043-55-2
3,3,4,4,5,5,6,6,6-nonafluorohexyliodide
-
19430-93-4
3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene
-
80793-18-6
3-(perfluorohexyl)prop-1-ene
-
25015-63-8
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane
2043-47-2 Downstream products
-
1799-84-4
3,3,4,4,5,5,6,6,6,-nonafluorohexyl methacrylate
-
353-50-4
Carbonyl fluoride
-
2706-90-3
Perfluoropentanoic acid
-
135984-67-7
3,3,4,4,5,5,6,6,6-Nonafluoro-hexanal
Relevant Products
-
Trifluoromethanesulfonic acidCAS：1493-13-6
-
1,10-Decanediol dimethacrylateCAS：6701-13-9
-
1-N-Boc-trans-1,4-cyclohexyldiamineCAS：177906-48-8
