2-Bromo-1,2-bis(4-butoxyphenyl)ethanone | 66659-80-1

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二苯乙烯类
• 英文名称: 2-Bromo-1,2-bis(4-butoxyphenyl)ethanone
• CAS: 66659-80-1
• 化学式: C₂₂H₂₇BrO₃
• 分子量: 419.359
• InChiKey: DMJALBLZAUAKGA-UHFFFAOYSA-N

物化性质

• 沸点：
  509.8±45.0 °C(Predicted)
• 密度：
  1.223±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6.5
• 重原子数：
  26
• 可旋转键数：
  11
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-Bromo-1,2-bis(4-butoxyphenyl)ethanone 在 tetrafluoroboric acid 、 高氯酸 、 tetraphosphorus decasulfide 作用下， 以 溶剂黄146 为溶剂， 反应 30.0h， 生成 1-[4,5-bis(4-butoxyphenyl)-1,3-dithiol-2-ylidene]piperidin-1-ium;perchlorate
  参考文献：
  名称：

  Polycarpe, Catherine; Torreilles, Eliane; Giral, Louis, Journal of Heterocyclic Chemistry, 1984, vol. 21, p. 1741 - 1745

  摘要：

  DOI：
• 作为产物：
  描述：

  4,4'-dibutoxy-deoxybenzoin 在 溴 作用下， 以 乙醚 为溶剂， 反应 1.0h， 以96%的产率得到2-Bromo-1,2-bis(4-butoxyphenyl)ethanone
  参考文献：
  名称：

  Polycarpe, Catherine; Torreilles, Eliane; Giral, Louis, Journal of Heterocyclic Chemistry, 1984, vol. 21, p. 1741 - 1745

  摘要：

  DOI：

文献信息

• 5,6-Diaryl-2,3-dihydroimidazo[2,1-b]thiazoles: a new class of immunoregulatory antiinflammatory agents
  作者：Paul E. Bender、David Hill、Priscilla H. Offen、Kazys Razgaitis、Patricia Lavanchy、Orum D. Stringer、Blaine M. Sutton、Don E. Griswold、Michael DiMartino

  DOI：10.1021/jm00147a008

  日期：1985.9

  A series of substituted 5,6-diaryl-2,3-dihydroimidazo[2,1-b]thiazoles were synthesized and evaluated in the rat adjuvant-induced arthritis and mouse oxazolone-induced contact sensitivity assays to determine the potential of these compounds for use as immunoregulatory antiinflammatory agents. This class of compounds was derived by combining salient structural features of the antiinflammatory agent flumizole and the immunoregulatory drug levamisole. Unlike the latter two, a number of compounds in the target series were found to possess the desired combination of activities. Exploration of structure-activity relationships in the adjuvant-induced arthritic rat assay revealed that optimal potency was exhibited by symmetrically substituted 5,6-diaryl compounds having one of the following alkyl heteroatom or halogen functions at the para position: methoxy, ethoxy, methylthio, N-ethyl-N-methylamino, fluoro, or chloro. Scrambling of these two substituent classes to yield the asymmetrically substituted 5,6-diaryl compounds resulted in potent activity only with the 5-alkyl heteroatom, 6-halo-substituted regioisomers. However in the oxazolone-induced contact sensitivity assay, no consistent relationship of variation in activity with structural change was apparent. The initial target compound 5,6-bis(4-methoxyphenyl)-2,3-dihydroimidazo[2,1-b]thiazole (1) was compared with its progenitors in additional models of inflammation and immunoregulation.
• POLYCARPE, C.;TORREILLES, E.;GIRAL, L.;BABEAU, A.;TINH, NGUYEN-HUN;GASPAR+, J. HETEROCYCL. CHEM., 1984, 21, N 6, 1741-1745
  作者：POLYCARPE, C.、TORREILLES, E.、GIRAL, L.、BABEAU, A.、TINH, NGUYEN-HUN、GASPAR+

  DOI：——

  日期：——
• Polycarpe, Catherine; Torreilles, Eliane; Giral, Louis, Journal of Heterocyclic Chemistry, 1984, vol. 21, p. 1741 - 1745
  作者：Polycarpe, Catherine、Torreilles, Eliane、Giral, Louis、Babeau, Annick、Tinh, Nguyen-Hun、Gasparoux, Henri

  DOI：——

  日期：——