6-chloro-5-nitroquinoxaline | 150536-27-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: 6-chloro-5-nitroquinoxaline
• 英文别名: 6-Chloro-5-nitro-quinoxaline
• CAS: 150536-27-9
• 化学式: C₈H₄ClN₃O₂
• 分子量: 209.592
• InChiKey: NYUBILNUCGYUEC-UHFFFAOYSA-N

物化性质

• 沸点：
  362.3±37.0 °C(Predicted)
• 密度：
  1.566±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  14
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  71.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  6-chloro-5-nitroquinoxaline 以 乙醇 为溶剂， 生成 6-chloro-5-hydroxyquinoxaline
  参考文献：
  名称：

  Phototransformations of 6-X-5-Nitroquinoxalines

  摘要：

  Photophysical properties and photochemical activity of 6-X-5-nitroquinoxalines with electrondonor substituents (X = H, CH3, Cl, OC2H5, NH2) ortho to the nitro group were studied. The quantum yield of the formation of 5-hydroxyquinoxaline from the corresponding nitro derivative depends on the nature of the substituent and irradiation conditions. Phototransformations can go through nitro-nitrite rearrangement with the participation of two alternative T(pipi*) levels, depending on the size and electronic effects of the substituent. The latter factor is largely determined by the population on excitation of different charge-transfer states involving the nitro group.

  DOI：

  10.1023/b:rugc.0000030402.66220.55
• 作为产物：
  描述：

  6-氯-2,1,3-苯并硒二唑 在 盐酸 、 sodium nitrate 、 硫酸 、 氢碘酸 作用下， 以 乙醇 、 水 为溶剂， 反应 3.0h， 生成 6-chloro-5-nitroquinoxaline
  参考文献：
  名称：

  Phototransformations of 6-X-5-Nitroquinoxalines

  摘要：

  Photophysical properties and photochemical activity of 6-X-5-nitroquinoxalines with electrondonor substituents (X = H, CH3, Cl, OC2H5, NH2) ortho to the nitro group were studied. The quantum yield of the formation of 5-hydroxyquinoxaline from the corresponding nitro derivative depends on the nature of the substituent and irradiation conditions. Phototransformations can go through nitro-nitrite rearrangement with the participation of two alternative T(pipi*) levels, depending on the size and electronic effects of the substituent. The latter factor is largely determined by the population on excitation of different charge-transfer states involving the nitro group.

  DOI：

  10.1023/b:rugc.0000030402.66220.55

文献信息

• Tian, Wei; Grivas, Spiros, Journal of Heterocyclic Chemistry, 1992, vol. 29, # 5, p. 1305 - 1308
  作者：Tian, Wei、Grivas, Spiros

  DOI：——

  日期：——
• Phototransformations of 6-X-5-Nitroquinoxalines
  作者：N. I. Rtishchev、A. V. Selitrennikov

  DOI：10.1023/b:rugc.0000030402.66220.55

  日期：2004.3

  Photophysical properties and photochemical activity of 6-X-5-nitroquinoxalines with electrondonor substituents (X = H, CH3, Cl, OC2H5, NH2) ortho to the nitro group were studied. The quantum yield of the formation of 5-hydroxyquinoxaline from the corresponding nitro derivative depends on the nature of the substituent and irradiation conditions. Phototransformations can go through nitro-nitrite rearrangement with the participation of two alternative T(pipi*) levels, depending on the size and electronic effects of the substituent. The latter factor is largely determined by the population on excitation of different charge-transfer states involving the nitro group.