硝基环己三烯 | 2395-99-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 硝基环己三烯
• 英文名称: 4-nitrophenyl radical
• 英文别名: p-Nitrophenyl radical；p-Nitro-phenyl-Radikal；4-Nitro-phenylradikal；p-Nitrophenyl-Radikal；p-Nitrophenylradikal；para-Nitrophenyl
• CAS: 2395-99-5
• 化学式: C₆H₄NO₂
• 分子量: 122.103
• InChiKey: ZHCAAFJSYLFLPX-UHFFFAOYSA-N

物化性质

• 熔点：
  86 °C

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  9
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  45.8
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  硝基环己三烯 在 二溴甲烷 作用下， 生成 1-溴-4-硝基苯
  参考文献：
  名称：

  Tilset, Mats; Parker, Vernon D., Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 1982, vol. 36, # 2, p. 123 - 124

  摘要：

  DOI：
• 作为产物：
  描述：

  4-硝基氯化重氮苯 在 methanol radical 作用下， 生成 硝基环己三烯
  参考文献：
  名称：

  Packer, John E.; Moenig, Joerg; Dobson, Brian C., Australian Journal of Chemistry, 1981, vol. 34, # 7, p. 1433 - 1441

  摘要：

  DOI：

文献信息

• Enemaerke, Rasmus J.; Christensen, Torben B.; Jensen, Henrik, Journal of the Chemical Society. Perkin Transactions 2 (2001), 2001, # 9, p. 1620 - 1630
  作者：Enemaerke, Rasmus J.、Christensen, Torben B.、Jensen, Henrik、Daasbjerg, Kim

  DOI：——

  日期：——
• Investigating the Mechanisms of Aromatic Amine-Induced Protein Free Radical Formation by Quantitative Structure−Activity Relationships: Implications for Drug-Induced Agranulocytosis
  作者：Arno G. Siraki、JinJie Jiang、Ronald P. Mason

  DOI：10.1021/tx900432d

  日期：2010.5.17

  Aromatic amine drugs have been associated with agranulocytosis (neutrophil depletion) for which the mechanism is unknown. We have previously shown that the metabolism of two aromatic amine drugs by human myeloperoxidase (MPO) results in phenyl radical metabolite formation and also in protein free radical formation on MPO. Because the concentration of drug required to produce a maximum signal for MPO protein free radical (MPO(center dot)) detection was different for each drug, this prompted us to consider that other aromatic amines may also show varying degrees of ability to induce MPO(center dot) formation. Immunoassay experiments using the immuno-spin-trapping technique were performed, which evaluated the potency of different aromatic amines containing the aniline substructure to generate the MPO(center dot). Each reaction contained equal amounts of H(2)O(2), 5,5-dimethyl-1-pyrroline-N-oxide, MPO, and variable concentrations of aniline derivatives. Several physicochemical parameters for aniline derivatives were used to derive quantitative structure-activity relationship equations, which showed that the Hammett constant (sigma) best correlated with the MPO(center dot) formation for all aniline derivatives. More statistically robust equations were derived if the anilines were separated into mono- and disubstituted groups. However, some aniline derivatives did not induce MPO(center dot) formation. Using electron spin resonance spectroscopy, we evaluated the ability of all aniline derivatives tested to produce phenyl radical metabolites, as previously shown by spin trapping for the aromatic amine drugs. Interestingly, we found that only those aniline derivatives that produced a phenyl radical also formed MPO(center dot). We propose that the phenyl radical is the reactive free radical metabolite responsible for generating the MPO(center dot).
• Parker, Vernon D., Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 1981, vol. 35, # 7, p. 533 - 536
  作者：Parker, Vernon D.

  DOI：——

  日期：——
• Packer, John E.; Heigway, Christopher J.; Miller, Helen M., Australian Journal of Chemistry, 1980, vol. 33, # 5, p. 965 - 977
  作者：Packer, John E.、Heigway, Christopher J.、Miller, Helen M.、Dobson, Brian C.

  DOI：——

  日期：——
• Rajkotia; Parsania, Journal of the Indian Chemical Society, 1999, vol. 76, # 1, p. 24 - 27
  作者：Rajkotia、Parsania

  DOI：——

  日期：——