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Dimethyl-[α-(ethoxy)-ethyliden]-ammonium-Ion | 41948-89-4

中文名称
——
中文别名
——
英文名称
Dimethyl-[α-(ethoxy)-ethyliden]-ammonium-Ion
英文别名
Dimethyl-<α-(ethoxy)-ethyliden>-ammonium-Ion;Methyl-dimethylamino-ethoxy-carbonium-hydroxid
Dimethyl-[α-(ethoxy)-ethyliden]-ammonium-Ion化学式
CAS
41948-89-4
化学式
BF4*C6H14NO
mdl
——
分子量
202.988
InChiKey
GOVICZOEEDQZRV-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

SDS

SDS:17184db1ba59c3d224270cb3ca9ec84c
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反应信息

  • 作为反应物:
    参考文献:
    名称:
    Meerwein,H. et al., Justus Liebigs Annalen der Chemie, 1961, vol. 641, p. 1 - 39
    摘要:
    DOI:
  • 作为产物:
    描述:
    N,N-二甲基乙酰胺 、 diphenylethylsulphonium tetrafluoroborate 反应 14.0h, 以70%的产率得到Dimethyl-[α-(ethoxy)-ethyliden]-ammonium-Ion
    参考文献:
    名称:
    O-alkylation d'amides A l'aide de sels d'alkyldiphenylsulfonium
    摘要:
    DOI:
    10.1016/s0040-4020(01)88543-4
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文献信息

  • Cardiac-slowing amidines containing the 3-thioindole group. Potential antianginal agents
    作者:Michael J. Zelesko、David F. McComsey、William E. Hageman、Samuel O. Nortey、Carol A. Baker、Bruce E. Maryanoff
    DOI:10.1021/jm00356a021
    日期:1983.2
    A series of 3-thioindolamidines (and 3-indolamidines) related to mixidine (1) was studied for cardiac-slowing properties, following the discovery of activity for prototype thioindole 2. Structure-activity relationships were explored, leading to many potent antitachycardiac agents (6-9, 12, 13, 15-17, 20, 23, 24, 30, 34, 35, 45, and 47-49). Relative to 2, cardiac-slowing activity is enhanced by substitution of the indole nitrogen with small (C1-C3) saturated alkyl groups (6-9), unsaturated alkyl groups (12, 13, and 15-17), or a methoxyethyl group (20); replacement of the N-methyl group with alkyl (23) or phenyl groups (24); and extension of the ethylene bridge by two methylene units (34). Dethio (i.e., 3-indole) analogues of 2 with alkyl substitution on the indole nitrogen (47-49) have greater activity as well. Several potent compounds were also found to have minimal myocardial depression (6-9, 13, 45, and 47). Secondary pharmacological testing is reported for thioindoles 2, 6, 7, 9, and 28.
  • Hydrolysis of N,N-disubstituted imidate esters
    作者:Vincent F. Smith、Gaston L. Schmir
    DOI:10.1021/ja00844a041
    日期:1975.5
  • Aumann, Rudolf; Hinterding, Peter, Chemische Berichte, 1990, vol. 123, p. 611 - 620
    作者:Aumann, Rudolf、Hinterding, Peter
    DOI:——
    日期:——
  • Plieninger,H. et al., Chemische Berichte, 1971, vol. 104, p. 3983 - 3985
    作者:Plieninger,H. et al.
    DOI:——
    日期:——
  • Issleib, Kurt; Leissring, Elke; Riemer, Manfred, Zeitschrift fur Chemie, 1983, vol. 23, # 3, p. 99 - 100
    作者:Issleib, Kurt、Leissring, Elke、Riemer, Manfred、Oehme, Hartmut
    DOI:——
    日期:——
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