isopropyl 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoate
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
Conditions | Yield |
---|---|
With RuCl2(DPPEA)(±DAIPEN); hydrogen; sodium methylate In isopropyl alcohol; benzene at 100℃; under 750.075 - 45004.5 Torr; for 40h; Autoclave; | 95% |
Conditions | Yield |
---|---|
With diethyl ether; pyrographite; ruthenium at 175℃; under 257428 Torr; Hydrogenation; | |
Multi-step reaction with 2 steps 1: 90 percent / thionyl chloride, N,N-dimethylformamide / 4 h / Heating 2: 77 percent / sodium bis(2-methoxyethoxy)aluminum hydride / diethyl ether; toluene / 0.5 h / Heating View Scheme | |
Multi-step reaction with 2 steps 1: chloroform 2: lithium alanate; diethyl ether View Scheme |
pentadecafluorooctanoyl chloride
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
Conditions | Yield |
---|---|
With sodium bis(2-methoxyethoxy)aluminium dihydride In diethyl ether; toluene for 0.5h; Heating; | 77% |
With lithium aluminium tetrahydride; diethyl ether |
Conditions | Yield |
---|---|
With formic acid; water-d2; ruthenium trichloride; triphenylphosphine at 200℃; for 8h; | |
With hydrogen; water-d2; 5 wt% Ru/C at 160℃; under 44134.3 Torr; for 8h; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride |
pentadecafluoro-octanoic acid butyl ester
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
2-bromoisobutyric acid bromide
Conditions | Yield |
---|---|
With dmap; triethylamine In tetrahydrofuran at 20℃; | 97% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
1-Hexadecanol
Conditions | Yield |
---|---|
With tributylphosphine; 1,1'-azodicarbonyl-dipiperidine In benzene at 65℃; for 2h; | 96% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
3-chloroprop-1-ene
8-(allyloxyl)-1,1,1,2,2,3,3,4,4,5,5,6,6,7,7-pentadecafluorooctane
Conditions | Yield |
---|---|
With sodium hydroxide; tetramethylammonium hydrogen sulfate at 40℃; for 12h; | 96% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
Nonafluorobutanesulfonyl fluoride
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluorooctyl nonafluorobutanesulfonate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; | 96% |
With triethylamine In diethyl ether | 95% |
With triethylamine In diethyl ether at 0 - 20℃; for 24h; | 95% |
With triethylamine In dichloromethane at -15℃; | 49% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
bromoacetic acid
1H,1H-perfluorooctyloxyacetic acid
Conditions | Yield |
---|---|
Stage #1: 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol With sodium hydride In tetrahydrofuran at 20℃; for 1.5h; deprotonation; Stage #2: bromoacetic acid In tetrahydrofuran at 20℃; for 24h; Alkylation; | 96% |
Conditions | Yield |
---|---|
With tributylphosphine; 1,1'-azodicarbonyl-dipiperidine In benzene for 2h; Ambient temperature; | 95% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
trifluoromethylsulfonic anhydride
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-n-octyl trifluoromethanesulfonate
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 0 - 20℃; | 91.5% |
With triethylamine In diethyl ether at -50 - 0℃; for 0.333333h; | |
With pyridine In dichloromethane at 0 - 20℃; Inert atmosphere; | |
With pyridine In dichloromethane |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
trifluoromethane sulfonyl chloride
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-n-octyl trifluoromethanesulfonate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 6h; Ambient temperature; | 90% |
With triethylamine In dichloromethane for 1h; Ambient temperature; | 85% |
With triethylamine In dichloromethane |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
Hexamethylphosphorous triamide
Conditions | Yield |
---|---|
With potassium hexafluorophosphate; tetrachloromethane In tetrahydrofuran at -30℃; for 0.5h; | 90% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
<(4-nitrophenyl)oxy>sulfonyl isocyanate
Conditions | Yield |
---|---|
at 20℃; for 0.0166667h; Addition; | 90% |
Conditions | Yield |
---|---|
With sodium hydroxide; tert-butyl alcohol at 65 - 70℃; for 7h; | 90% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
isocyanate de chloro-4 phenoxysulfonyle
Conditions | Yield |
---|---|
at 20℃; for 0.0166667h; Addition; | 89% |
para-dinitrobenzene
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
4-nitro-1-(2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctyloxy)benzene
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In N,N-dimethyl-formamide at 20℃; for 2h; | 89% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
Thioctic acid
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; Cooling with ice; | 88% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
1,1,1,3,3,3-hexamethyl-disilazane
Conditions | Yield |
---|---|
With saccharin sodium salt at 80 - 90℃; for 2h; | 87.5% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
isocyanatosulfuric acid 2,6-dimethyl-phenyl ester
Conditions | Yield |
---|---|
at 20℃; for 0.416667h; Addition; | 87% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
tetrakis(pentafluorophenyl)porphyrin
Conditions | Yield |
---|---|
With potassium hydroxide In tetrahydrofuran at 20℃; for 24h; Inert atmosphere; regioselective reaction; | 87% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
malonoyl dichloride
bis (1.1-dihydroperfluorooctyl) malonate
Conditions | Yield |
---|---|
In toluene | 86.5% |
In toluene | 86.5% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
Fluorosulfuric acid pentadecafluoroheptyl ester
Conditions | Yield |
---|---|
With potassium fluorosulfonate; fluorosulphonic acid at 25℃; anodic oxidation; 6.5 F/mol; | 85% |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
propargyl bromide
3-((1-perfluoroheptyl)methoxy)prop-1-yne
Conditions | Yield |
---|---|
With sodium hydroxide In tetrahydrofuran at 20℃; Cooling with ice; | 85% |
With sodium hydroxide In tetrahydrofuran at 20℃; |
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octanol
p-toluenesulfonyl chloride
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-1-octyl 4-toluenesulfonate
Conditions | Yield |
---|---|
With potassium hydroxide In diethyl ether at -4℃; for 24h; | 85% |
With triethylamine In dichloromethane at 0 - 20℃; | 77% |
IUPAC Name: 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluorooctan-1-ol
Product Name: 1H,1H-Pentadecafluoro-1-octanol
The MF of 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluorooctan-1-ol (CAS NO.307-30-2) is C8H3F15O.
The MW of 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluorooctan-1-ol (CAS NO.307-30-2) is 400.08.
Synonyms of 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluorooctan-1-ol (CAS NO.307-30-2): 1-Octanol, 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro- ; 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluorooctan-1-ol ; 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluorooctyl alcohol ; 1H,1H-Pentadecafluoro-1-octanol ; 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluoro-1-octanol
Product Categories: Fluorous Chemistry;Fluorous Compounds;Synthetic Organic Chemistry;Fluorous Synthesis;Rf-Tagged Building Blocks and Precursors
Apperance: white crystalline mass
Index of Refraction: 1.285
EINECS: 206-197-1
Density: 1.665 g/ml
Flash Point: 49.2 °C
Boiling Point: 164 °C
Melting Point: 38-40 °C
BRN: 1716494
2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluorooctan-1-ol (CAS NO.307-30-2) is used as fine chemicals, chemical synthesis, medicine, pesticide intermediates.
Safety information of 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluorooctan-1-ol (CAS NO.307-30-2):
Hazard Codes Xi
Risk Statements
36/37/38 Irritating to eyes, respiratory system and skin
Safety Statements
26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36 Wear suitable protective clothing
WGK Germany 3
Hazard Note Irritant
TSCA T
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