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(E)-3,4,3',4'-Tetramethyl-3H,3'H-[2,2']bithiazolylidene | 131352-71-1

中文名称
——
中文别名
——
英文名称
(E)-3,4,3',4'-Tetramethyl-3H,3'H-[2,2']bithiazolylidene
英文别名
(2E)-2-(3,4-dimethyl-1,3-thiazol-2-ylidene)-3,4-dimethyl-1,3-thiazole
(E)-3,4,3',4'-Tetramethyl-3H,3'H-[2,2']bithiazolylidene化学式
CAS
131352-71-1
化学式
C10H14N2S2
mdl
——
分子量
226.367
InChiKey
MZRAVWQJADLTRN-MDZDMXLPSA-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):
    3.19
  • 重原子数:
    14.0
  • 可旋转键数:
    0.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    6.48
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    参考文献:
    名称:
    Acidities of C2 hydrogen atoms in thiazolium cations and reactivities of their conjugate bases
    摘要:
    The equilibrium acidity for the C2-H bond in the 3,4-dimethylthiazolium cation (TZCH+), a model for thiamin, was estimated to be higher than 16 by direct titrations with indicators in DMSO solution. This result is in agreement with several earlier indirect estimates based on kinetic acidities and Bronsted plots, which place the acidity in the 16-20 pK(HA+) region in aqueous solution, but not with a direct titration in aqueous medium made under stopped-flow conditions, which placed the acidity in the region of pK(HA+) almost-equal-to 13. 3-Methylbenzothiazolium cation (BZCH+), which was found to be considerably more acidic, reacted with Et3N in DMSO to give a dimer BZC=CZB. Evidence is presented to show that this and similar dimerizations occur by addition of the conjugate base of BZCH+ to the H-C=N+ bond to the BZCH+ thiazolium cation, followed by deprotonation. The conjugate base of BZCH+ adds to BZCH+ in preference to reacting with excess of electrophiles such as t-buOH, PhCHO, or PhCH=CH2. Amines, such as piperidine, add rapidly to less acidic thiazolium cations under conditions where little or no deprotonation occurs. These observations exclude a carbene mechanism for dimerization and amine adduct formation.
    DOI:
    10.1021/ja00003a036
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文献信息

  • BORDWELL, F. G.;SATISH, A. V., J. AMER. CHEM. SOC., 113,(1991) N, C. 985-990
    作者:BORDWELL, F. G.、SATISH, A. V.
    DOI:——
    日期:——
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