추천 제품
Quality Level
분석
96%
형태
liquid
반응 적합성
reaction type: click chemistry
refractive index
n20/D 1.3 (lit.)
bp
64 °C (lit.)
density
1.682 g/mL at 25 °C (lit.)
작용기
fluoro
SMILES string
FC(F)(F)C(F)(F)C(F)(F)C(F)(F)S(F)(=O)=O
InChI
1S/C4F10O2S/c5-1(6,3(9,10)11)2(7,8)4(12,13)17(14,15)16
InChI key
LUYQYZLEHLTPBH-UHFFFAOYSA-N
애플리케이션
Perfluoro-1-butanesulfonyl fluoride (NfF) reacts with alcohols, including phenols, to yield nonafluorobutanesulfonate esters (nonaflates). Nonaflates can be used as electrophiles in several palladium-catalyzed cross coupling reactions and in Buchwald-Hartwig amination.
NfF can also be used to prepare aryl nonaflates by reacting with corresponding aryloxysilanes in the presence of fluoride ion.
NfF can also be used to prepare aryl nonaflates by reacting with corresponding aryloxysilanes in the presence of fluoride ion.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Faceshields, Gloves, Goggles
이미 열람한 고객
Synthesis of polysubstituted olefins by Pd-catalyzed cross-coupling reaction of tosylhydrazones and aryl nonaflates.
Organic Letters, 13(3), 510-513 (2010)
Hydrierende Spaltung phenolischer und enolischer Perfluoroalkansulfonate.
Synthesis, 1984(06), 481-485 (1984)
Palladium-catalyzed amination of aryl nonaflates.
The Journal of Organic Chemistry, 68(25), 9563-9573 (2003)
Facile synthesis of trifluoro-and hexafluoroisopropyl halides.
The Journal of Organic Chemistry, 54(6), 1432-1435 (1989)
Uber Perfluoralkansulfonsaurearylester.
European Journal of Organic Chemistry, 1973(1), 20-32 (1973)
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