2-chloro-3,5-dinitro-benzaldehyde | 713124-98-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-chloro-3,5-dinitro-benzaldehyde
• 英文别名: 2-chloro-3,5-dinitrobenzaldehyde；2-Chlor-3,5-dinitro-benzaldehyd；2-Chloro-3,5-dinitrobenzaldehyde
• CAS: 713124-98-2
• 化学式: C₇H₃ClN₂O₅
• 分子量: 230.564
• InChiKey: JQZGBYRJYHYFSG-UHFFFAOYSA-N

物化性质

• 熔点：
  78 °C
• 沸点：
  345.8±42.0 °C(Predicted)
• 密度：
  1.686±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  15
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  109
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-chloro-3,5-dinitro-benzaldehyde 、 甲胺 以 甲醇 、 乙醇 为溶剂， 反应 12.0h， 以76%的产率得到2-methylamino-3,5-dinitro-benzaldehyde
  参考文献：
  名称：

  Efficient synthesis and fluorescence properties of highly functionalized 2-aryl-quinazolin-4(3H)-ones

  摘要：

  Three different methodologies for the preparation of highly substituted 2-aryl-quinazolin-4(3H)-ones including short and high-yielding reaction sequences are described. The 2-aryl-substituent of most of the target compounds bears three functional groups. The fluorescence properties of these compounds are presented and potential correlations between structure and optical properties are discussed. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2009.03.139
• 作为产物：
  描述：

  2-氯-1-甲基-3,5-二硝基苯 生成 2-chloro-3,5-dinitro-benzaldehyde
  参考文献：
  名称：

  Mittal, Journal of the Indian Chemical Society, 1942, vol. 19, p. 408

  摘要：

  DOI：

文献信息

• Kawabata, Takeo; Jiang, Changsheng; Hayashi, Kazuhiro, Journal of the American Chemical Society, 2009, vol. 131, p. 54 - 55
  作者：Kawabata, Takeo、Jiang, Changsheng、Hayashi, Kazuhiro、Tsubaki, Kazunori、Yoshimura, Tomoyuki、et al.

  DOI：——

  日期：——
• Mittal, Proceedings of the Indian National Science Academy, 1946, vol. 15 A, p. 10
  作者：Mittal

  DOI：——

  日期：——
• Hydroxamic Acid Derivatives
  申请人：Chen Yu

  公开号：US20110269706A1

  公开（公告）日：2011-11-03

  The disclosure includes hydroxamic compounds of Formula I: (I) wherein P, Z, and m are defined herein. Also disclosed is a method for treating a neoplastic disease or an immune disease with these compounds.
• Efficient synthesis and fluorescence properties of highly functionalized 2-aryl-quinazolin-4(3H)-ones
  作者：Michael Waibel、Jens Hasserodt

  DOI：10.1016/j.tetlet.2009.03.139

  日期：2009.6

  Three different methodologies for the preparation of highly substituted 2-aryl-quinazolin-4(3H)-ones including short and high-yielding reaction sequences are described. The 2-aryl-substituent of most of the target compounds bears three functional groups. The fluorescence properties of these compounds are presented and potential correlations between structure and optical properties are discussed. (C) 2009 Elsevier Ltd. All rights reserved.
• Mittal, Journal of the Indian Chemical Society, 1942, vol. 19, p. 408
  作者：Mittal

  DOI：——

  日期：——