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二甲基氟离子 | 64710-12-9

分子结构分类

中文名称
二甲基氟离子
中文别名
——
英文名称
dimethylfluoronium ion
英文别名
dimethylfluoronium;Dimethyl-fluorid-kation
二甲基氟离子化学式
CAS
64710-12-9
化学式
C2H6F
mdl
——
分子量
49.068
InChiKey
YUVJHFIUYFHNGZ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.33
  • 重原子数:
    3.0
  • 可旋转键数:
    0.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

SDS

SDS:fc579c628b022bea2b9acc0ca8170232
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反应信息

  • 作为反应物:
    参考文献:
    名称:
    Site of gas-phase methylation of l-phenyl-2-aminopropane
    摘要:
    AbstractThe regioselectivity of methyl cation transfer from (CH3)2F+, (CH3)2Cl+ and (CH3)3O+ to 1‐phenyl‐2‐aminopropane was studied by Fourier transform ion cyclotron resonance in combination with collision‐induced dissociation and neutralization‐reionization mass spectrometry of the stable [M + CH3]+ ions formed in a chemical ionization source. The (CH3)2F+ ion transfers a methyl cation to the NH2 group and the phenyl ring with almost equal probability. Predominant CH3+ transfer to the NH2 group is observed for the (CH3)2Cl+ ion whereas the (CH3)3O+ ion reacts almost exclusively at the amino group. The preference for methylation at NH2 is discussed in terms of a lower methyl cation affinity of the phenyl ring than of the amino group and the existence of an energy barrier for methylation of the phenyl moiety.
    DOI:
    10.1002/oms.1210260610
  • 作为产物:
    描述:
    氟甲烷 作用下, 生成 二甲基氟离子
    参考文献:
    名称:
    Methyl cation affinities
    摘要:
    DOI:
    10.1021/ja00231a002
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文献信息

  • Gas-phase heteroaromatic substitution. 3. Electrophilic methylation of furan and thiophene by CH<sub>3</sub>XCH<sub>3+</sub> (X = fluoro, chloro) ions
    作者:Giancarlo Angelini、Gaetano Lilla、Maurizio Speranza
    DOI:10.1021/ja00389a035
    日期:1982.12
    CH/sub 3/ClCH/sub 3//sup +/ confirms its inherent affinity toward n-type nucleophilic centers by attacking preferentially the heteroatom of 3 and 4. In light of the previous results concerning CH/sub 3/XCH/sub 3//sup +/ methylation of pyrroles, it is concluded that gas-phase attack of CH/sub 3/XCH/sub 3//sup +/ on simple five-membered heteroaromatics is essentially regulated by the electrostatic interaction
    先前对 CH/sub 3/XCH/sub 3//sup +/ (X = F 或 Cl) 离子对吡咯N-甲基吡咯的气相甲基化进行的辐解研究,来自 CH 的 ..gamma.. 辐解/sub 3/X,扩展为呋喃 (3) 和噻吩 (4)。讨论了通过分子内 1,2 甲基转移发生的取代和随后异构化的机制,并评估了所选亲电子物种的底物和位置选择性。至于吡咯呋喃噻吩的气相CH/sub 3/FCH/sub 3//sup +/甲基化的特点是缺乏底物区分(k/sub S//k/sub B/ = 1.2 (3) , 0.8 (4)),伴随着对具有最高负净电荷的底物位置的明显位置选择性(O:..cap alpha..:..beta.. = 36%:35%:29% for 3; S:..cap alpha..:..beta.. = 19%:43%:38% for 4)。相反,CH/sub 3/ClCH/sub
  • Gas-phase protonation and methyl cation transfer from methyl halide ions
    作者:R. Houriet、E. Rolli、R. Flammang、A. Maquestiau、G. Bouchoux
    DOI:10.1002/oms.1210221203
    日期:1987.12
    AbstractThe ion‐molecule reactions between [CH3X]+˙ [CH3XH] +, [CH3XCH3]+ ions (X = F, Cl, Br, I) and a number of nucleophiles have been studied by ion cyclotron resonance techniques. Protonation of the nucleophiles is observed to occur from both the molecular ions [CH3]X+˙ and protonated species [CH3XH]+ whereas dimethylhalonium ions [CH3XCH3]+ react principally by methyl cation transfer. A notable exception occurs in methyl iodide where the molecular ions [CH3I]+˙ act both as proton and methyl cation donors, whereas dimethyliodonium ions are found unreactive. The results are discussed with reference to the use of alkyl halides as reagent gases in chemical ionization experiments.
  • Gas-phase heteroaromatic substitution. 2. Electrophilic methylation of pyrrole and N-methylpyrrole by CH<sub>3</sub>XCH<sub>3</sub><sup>+</sup> (X = fluoro, chloro) ions
    作者:Giancarlo Angelini、Cinzia Sparapani、Maurizio Speranza
    DOI:10.1021/ja00389a034
    日期:1982.12
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同类化合物

()-2-(5-甲基-2-氧代苯并呋喃-3(2)-亚乙基)乙酸乙酯 (甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (反式)-4-壬烯醛 (双(2,2,2-三氯乙基)) (乙腈)二氯镍(II) (乙基N-(1H-吲唑-3-基羰基)ethanehydrazonoate) (βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (±)17,18-二HETE (±)-辛酰肉碱氯化物 (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (s)-2,3-二羟基丙酸甲酯 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 ([2-(萘-2-基)-4-氧代-4H-色烯-8-基]乙酸) ([1-(甲氧基甲基)-1H-1,2,4-三唑-5-基](苯基)甲酮) (Z)-5-辛烯甲酯 (Z)-4-辛烯醛 (Z)-4-辛烯酸 (Z)-3-[[[2,4-二甲基-3-(乙氧羰基)吡咯-5-基]亚甲基]吲哚-2--2- (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-(-)-5'-苄氧基苯基卡维地洛 (S)-(-)-2-(α-(叔丁基)甲胺)-1H-苯并咪唑 (S)-(-)-2-(α-甲基甲胺)-1H-苯并咪唑 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-(+)-5,5'',6,6'',7,7'',8,8''-八氢-3,3''-二叔丁基-1,1''-二-2-萘酚,双钾盐 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-盐酸沙丁胺醇 (S)-溴烯醇内酯 (S)-氨氯地平-d4 (S)-氨基甲酸酯β-D-O-葡糖醛酸 (S)-8-氟苯并二氢吡喃-4-胺 (S)-7,7-双[(4S)-(苯基)恶唑-2-基)]-2,2,3,3-四氢-1,1-螺双茚满 (S)-4-(叔丁基)-2-(喹啉-2-基)-4,5-二氢噁唑 (S)-4-氯-1,2-环氧丁烷 (S)-3-(((2,2-二氟-1-羟基-7-(甲基磺酰基)-2,3-二氢-1H-茚满-4-基)氧基)-5-氟苄腈 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-3-(2-(二氟甲基)吡啶-4-基)-7-氟-3-(3-(嘧啶-5-基)苯基)-3H-异吲哚-1-胺 (S)-2-(环丁基氨基)-N-(3-(3,4-二氢异喹啉-2(1H)-基)-2-羟丙基)异烟酰胺 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[[[(1R,2R)-2-[[[3,5-双(叔丁基)-2-羟基苯基]亚甲基]氨基]环己基]硫脲基]-N-苄基-N,3,3-三甲基丁酰胺 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-2-N-Fmoc-氨基甲基吡咯烷盐酸盐 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (SP-4-1)-二氯双(喹啉)-钯 (SP-4-1)-二氯双(1-苯基-1H-咪唑-κN3)-钯