氯对苯二甲酸

氯对苯二甲酸是一种有机化合物,化学式为C8H5ClO4。它可由2-氯-4-甲基苯乙酮和高锰酸钾[1]氯对二甲苯硝酸[2]的氧化反应制得。它和混酸(H2SO4/HNO3)反应,可以得到2-氯-5-硝基-1,4-苯二甲酸。[3]它可用于构筑金属有机框架材料[4]

氯对苯二甲酸
识别
CAS号 1967-31-3  checkY
PubChem 74785
性质
化学式 C8H5ClO4
摩尔质量 200.58 g·mol−1
外观 无色固体[1]
熔点 316—317 °C(589—590 K)[1]
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

参考文献 编辑

  1. ^ 1.0 1.1 1.2 Robert E. Lutz, Rufus K. Allison, Gilbert Ashburn, Philip S. Bailey, Marion T. Clark, John F. Codington, Adolf J. Deinet, James A. Freek, Robert H. Jordan, Norman H. Leake, Tellis A. Martin, Kent C. Nicodemus, Russell J. Rowlett, Newton H. Shearer, J. Doyle Smith, James W. Wilson. ANTIMALARIALS. α-PHENYL-β-DIALKYLAMINO ALCOHOLS 1. The Journal of Organic Chemistry. 1947-09, 12 (5): 673 [2022-12-16]. ISSN 0022-3263. doi:10.1021/jo01169a001. (原始内容存档于2022-12-16) (英语). 
  2. ^ Martin Lammert, Michael T. Wharmby, Simon Smolders, Bart Bueken, Alexandra Lieb, Kirill A. Lomachenko, Dirk De Vos, Norbert Stock. Cerium-based metal organic frameworks with UiO-66 architecture: synthesis, properties and redox catalytic activity. Chemical Communications. 2015, 51 (63): 12578–12581 [2022-12-16]. ISSN 1359-7345. doi:10.1039/C5CC02606G (英语). 
  3. ^ Schulz, Mark James; Wang, Yonghui. Prolyl hydroxylase inhibitors. 2010 WO 2010059549 A1.
  4. ^ Weibin Liang, Ravichandar Babarao, Deanna M. D’Alessandro. Microwave-Assisted Solvothermal Synthesis and Optical Properties of Tagged MIL-140A Metal–Organic Frameworks. Inorganic Chemistry. 2013-11-18, 52 (22): 12878–12880 [2022-12-16]. ISSN 0020-1669. doi:10.1021/ic4024234. (原始内容存档于2022-12-16) (英语).