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1)  Perfluoroalkylethyl
多氟烷基乙基
1.
Synthesis and Biological Activity of N-2-Perfluoroalkylethyl-substituted or Glucopyranosyl-substituted Triazole Derivatives;
多氟烷基乙基和葡萄糖基取代的三唑类化合物的合成及生物活性研究
2)  perfluoroalkyl
多氟烷基
1.
To improve their bioactivities of oxadiazole and triazole analogues,a series of N-2-perfluoroalkylethyl-substituted 1,3,4-oxadiazole-2-thiones 6a~6l and 1,2,4-triazole-5-thiones 9a~9l were synthesized and their structures were confirmed by 1H NMR,19F NMR,IR,MS spectra and elemental analysis.
为改善二唑及三唑类化合物的生物活性,设计合成了一系列多氟烷基乙基取代的1,3,4-噁二唑-2-硫酮6a~6l及1,2,4-三唑-5-硫酮类化合物9a~9l。
2.
On the basis of these Schiff bases, a series of 1-perfluoroalkyl-substituted or glycopyranosyl-substituted 2,4-dihydro- 1,2,4-triazole-3-thione Schiff bases (5a~5r, 6a~6d) were synthesized by the reaction of the Sch.
在此基础上,化合物4a~4i分别与多氟烷基碘代烷和溴代乙酰基葡萄糖反应合成了一系列2,4-二氢-1,2,4-三唑-3-硫酮类席夫碱的多氟烷基取代物5a~5r和葡萄糖基取代物6a~6d,并用1HNMR,19FNMR,IR和MS谱以及元素分析表征了它们的结构。
3.
Synthesis N-Perfluoroalkylethyl-substituted Oxadiazole, Triazole and Its Application of Quasiracemic Synthesis;
关于它们唑环NH上的氢原子的反应已有较多的研究,比较典型的就是Mannich反应,但是对于该氢原子被多氟烷基取代的化合物,却未有文献报道。
3)  polyfluoroalkyl iodide
多氟烷基碘代烷
1.
A new convenient synthesis of a series of polyfluoroalkyl substituted cyclopropane derivatives was achieved by the reaction of polyfluoroalkyl iodides with diethyl allylmalonate in the presence of sodium dithionite in 45%~55% yields.
以连二亚硫酸钠为引发剂,烯丙基丙二酸二乙酯与多氟烷基碘代烷在温和条件下反应,方便地得到一系列多氟烷基取代的环丙烷衍生物,产率45%~55%。
4)  2-fluoroalkylacetic acid
2-氟烷基乙酸
5)  Perfluoroalkyl alcohol
全氟烷基乙醇
6)  methoxyflurane [me,θɔksi'fluərein]
甲氧基氟氯乙烷
补充资料:(氰基-1-甲基乙基)十二烷基乙基锍四氟代硼酸盐
CAS:72140-65-9
中文名称:(氰基-1-甲基乙基)十二烷基乙基锍四氟代硼酸盐

英文名称:(Cyano-1-methylethyl)dodecylethylsulphoniumtetrafluoroborate
(2-cyano-1-methylethyl)dodecylethyl-sulfoniu tetrafluoroborate
(2-cyano-1-methylethyl)dodecylethyl-sulfoniutetrafluoroborate
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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