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N,N-dimethyl-N-<2-methyl-3-oxo-3-(2-thienyl)propyl>ammonium chloride | 2522-99-8

中文名称
——
中文别名
——
英文名称
N,N-dimethyl-N-<2-methyl-3-oxo-3-(2-thienyl)propyl>ammonium chloride
英文别名
3-dimethylamino-2-methyl-1-thiophen-2-yl-propan-1-one; hydrochloride;3-dimethylamino-2-methyl-1-[2]thienyl-propan-1-one; hydrochloride;3-Dimethylamino-2-methyl-1-[2]thienyl-propan-1-on; Hydrochlorid;3-Dimethylamino-2-methyl-1-(2-thienyl)-propan-1-on*HCl;Dimethyl-(2-methyl-3-oxo-3-thiophen-2-ylpropyl)azanium;chloride;dimethyl-(2-methyl-3-oxo-3-thiophen-2-ylpropyl)azanium;chloride
N,N-dimethyl-N-<2-methyl-3-oxo-3-(2-thienyl)propyl>ammonium chloride化学式
CAS
2522-99-8
化学式
C10H15NOS*ClH
mdl
——
分子量
233.762
InChiKey
JRYJVSZTTCIVMK-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):
    2.55
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    48.6
  • 氢给体数:
    1
  • 氢受体数:
    3

SDS

SDS:5f76cb88d3e8b7efac0e785e9d2cae09
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反应信息

  • 作为反应物:
    描述:
    N,N-dimethyl-N-<2-methyl-3-oxo-3-(2-thienyl)propyl>ammonium chloride硫酸四氯化钛 作用下, 以 四氢呋喃 为溶剂, 反应 6.0h, 生成 (6E)-5-methyl-6-(5-methyl-4,5-dihydrocyclopenta[b]thiophen-6-ylidene)-4,5-dihydrocyclopenta[b]thiophene
    参考文献:
    名称:
    Bridged Dithienylethylenes as Precursors of Small Bandgap Electrogenerated Conjugated Polymers
    摘要:
    Bridged dithienylethylenes (DTEs) bearing solubilizing alkyl chains at various positions (2-5) have been synthesized by McMurry dimerization of cyclopenta[b]thiophen-6-ones. In order to introduce alkyl substituents at different positions of the DTE molecule, the precursor ketones have been prepared by different strategies based on a combination of Mannich or Wittig-Horner reaction and Friedel-Craft intramolecular cyclization. The position and the length of the alkyl substituents exert a strong effect on the ability of the precursor to undergo electrochemical polymerization. Thus, whereas substitution at the alpha-position of the ethylene linkage (3) results in a rapid inhibition of electropolymerization, introduction of alkyl chains at the beta-position (4, 5) greatly improves the efficiency of the polymerization process. The analysis of the electrochemical and optical properties of the polymers shows that rigidification of the DTE molecule leads to a significant decrease of the oxidation potential and bandgap. A comparative analysis of DTE and its bridged analogues by means of X-ray diffraction reveals, in agreement with experimental and theoretical results, that the observed reduction of both the HOMO-LUMO gap of the precursor and the bandgap of the corresponding polymers are related to a relaxation of bond length alternation in the DTE moiety.
    DOI:
    10.1021/jo9623447
  • 作为产物:
    描述:
    1-(2-噻吩基)-1-丙酮聚合甲醛盐酸二甲胺盐酸乙醇 为溶剂, 反应 4.0h, 以49%的产率得到N,N-dimethyl-N-<2-methyl-3-oxo-3-(2-thienyl)propyl>ammonium chloride
    参考文献:
    名称:
    Bridged Dithienylethylenes as Precursors of Small Bandgap Electrogenerated Conjugated Polymers
    摘要:
    Bridged dithienylethylenes (DTEs) bearing solubilizing alkyl chains at various positions (2-5) have been synthesized by McMurry dimerization of cyclopenta[b]thiophen-6-ones. In order to introduce alkyl substituents at different positions of the DTE molecule, the precursor ketones have been prepared by different strategies based on a combination of Mannich or Wittig-Horner reaction and Friedel-Craft intramolecular cyclization. The position and the length of the alkyl substituents exert a strong effect on the ability of the precursor to undergo electrochemical polymerization. Thus, whereas substitution at the alpha-position of the ethylene linkage (3) results in a rapid inhibition of electropolymerization, introduction of alkyl chains at the beta-position (4, 5) greatly improves the efficiency of the polymerization process. The analysis of the electrochemical and optical properties of the polymers shows that rigidification of the DTE molecule leads to a significant decrease of the oxidation potential and bandgap. A comparative analysis of DTE and its bridged analogues by means of X-ray diffraction reveals, in agreement with experimental and theoretical results, that the observed reduction of both the HOMO-LUMO gap of the precursor and the bandgap of the corresponding polymers are related to a relaxation of bond length alternation in the DTE moiety.
    DOI:
    10.1021/jo9623447
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文献信息

  • 755. Some 1,2-diaryl-4-dimethylamino-3-methylbutan-2-ols and derivatives related to propoxyphene
    作者:A. F. Casy、J. L. Myers
    DOI:10.1039/jr9650004092
    日期:——
  • AVRAMOVA, P.;ILARIONOV, J.;DRYANOVSKA, L., FARMATSIYA, 1985, 35, N 5, 6-12
    作者:AVRAMOVA, P.、ILARIONOV, J.、DRYANOVSKA, L.
    DOI:——
    日期:——
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