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CAS No.: | 30556-86-6 |
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Name: | 3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctylamine |
Article Data: | 14 |
Molecular Structure: | |
Formula: | C8H6F13N |
Molecular Weight: | 363.122 |
Synonyms: | 1-Octanamine,3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro;3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylamine;1H,1H,2H,2H-perfluorooctylamine; |
PSA: | 26.02000 |
LogP: | 4.77430 |
8-azido-1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorooctane
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylamine
Conditions | Yield |
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With hydrogen; palladium on activated charcoal In diethyl ether at 20℃; under 5171.62 Torr; | 88% |
With hydrazine hydrate; nickel In water at 60℃; for 8h; | 83% |
With lithium aluminium tetrahydride In tetrahydrofuran | 77% |
1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylamine
Conditions | Yield |
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With sodium azide; N2H4*H2O-Raney Ni; hydrazine hydrate Multistep reaction; | |
Multi-step reaction with 2 steps 1: sodium azide; Aliquot 336 / H2O / Heating 2: H2 / Pd/C / diethyl ether / 2585.74 Torr View Scheme | |
Multi-step reaction with 2 steps 1: NaN3 / dimethylformamide / 72 h / 20 °C 2: 8.1 g / H2 / Pd/C / diethyl ether / 12 h / 5250.42 Torr View Scheme |
Conditions | Yield |
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With triethylamine In chloroform Solvent; Concentration; Cooling with ice; | 99% |
isocyanate de chloro-4 phenoxysulfonyle
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylamine
Conditions | Yield |
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In toluene at 0℃; for 0.0833333h; Addition; | 98% |
Glyoxal
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylamine
Conditions | Yield |
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In methanol at 20℃; for 48h; Condensation; | 98% |
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylamine
Isopropyl isocyanate
Conditions | Yield |
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In dichloromethane at 20℃; for 0.5h; | 95% |
2,2-bis(hydroxymethyl)propionic acid
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylamine
3-Hydroxy-2-hydroxymethyl-2-methyl-N-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyl)-propionamide
Conditions | Yield |
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With tertiary amine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate | 94% |
3-(tert-butyloxycarbonylamino)propionic acid
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylamine
C16H19F13N2O3
Conditions | Yield |
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Stage #1: 3-(tert-butyloxycarbonylamino)propionic acid With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 0.166667h; Stage #2: 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylamine In dichloromethane at 20℃; for 12h; | 94% |
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylamine
epichlorohydrin
Conditions | Yield |
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at 40 - 45℃; for 15h; | 93% |
Boc-Asp-OH
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylamine
Conditions | Yield |
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With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane | 92% |
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine In acetonitrile for 3h; Ambient temperature; | 66% |