ethyl tert-butyl phosphate

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 有机磷酸及其衍生物
• 英文名称: ethyl tert-butyl phosphate
• 英文别名: phosphoric acid tert-butyl ester ethyl ester；Ethyl-tert-butyl-phosphat；Tert-butyl ethyl hydrogen phosphate
• 化学式: C₆H₁₅O₄P
• 分子量: 182.156
• InChiKey: OATPTEJWZSGIME-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  11
• 可旋转键数：
  4
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  55.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  ethyl metaphosphate 、 叔丁醇 反应 7.0h， 生成 ethyl tert-butyl phosphate
  参考文献：
  名称：

  通过2,3-氧杂磷双环[2.2.2]辛-5-烯衍生物的光解生成偏磷酸的酯和酰胺衍生物

  摘要：

  在254 nm处照射P-NMe 2和P-OEt膦酸酯衍生物，其中P掺入2,3-氧杂磷双环[2.2.2] oct-5-ene骨架中，导致分子断裂，释放N，N-二甲基氨基偏氨基磷酸酯和偏磷酸乙酯。两种物质都迅速聚合，但是当反应混合物中包含醇时，它们会有效地被捕获为磷酸盐衍生物。

  DOI：

  10.1016/0040-4039(88)85244-4

文献信息

• Substituted Aminothiazole Prodrugs of Compounds with Anti-HCV Activity
  申请人：Liu Cuixan

  公开号：US20090304605A1

  公开（公告）日：2009-12-10

  The invention provides amino-substituted aminothiazole compounds of Formula I and Formula II where A is a group of the formula: and the variables X, Y, R, and R 1 to R 7 are described herein. These compounds are prodrugs of compounds useful as inhibitors of viral replication. Compositions containing such compounds, and methods of treating viral infections with these compounds, as well as to processes and intermediates useful for preparing such compounds are also provided by the invention.

  该发明提供了公式I和公式II的氨基取代氨噻唑化合物，其中A是以下式的基团：变量X、Y、R和R1至R7如本文所述。这些化合物是可用作抑制病毒复制的化合物的前药。该发明还提供了含有这些化合物的组合物，以及使用这些化合物治疗病毒感染的方法，以及用于制备这些化合物的过程和中间体。
• COMPOUNDS FOR TREATING BACTERIAL INFECTIONS
  申请人：Glaser Gad

  公开号：US20110086813A1

  公开（公告）日：2011-04-14

  The present invention relates to a novel class of guanine nucleotide analogs which inhibit RelA and Relseq synthetic activity and which possess anti-bacterial activity. The present invention also relates to pharmaceutical compositions that include such compounds, and to methods of use of such compounds or compositions for combating bacteria and treating bacterial infections.

  本发明涉及一类新型鸟嘌呤核苷酸类似物，其抑制RelA和Relseq的合成活性，并具有抗细菌活性。本发明还涉及包括这些化合物的药物组合物，以及利用这些化合物或组合物来对抗细菌和治疗细菌感染的方法。
• Studies in phosphorylation. Part XXIX. The synthesis of dialkyl phosphates from monoalkyl phosphonates: direct oxidative esterification
  作者：G. M. Blackburn、J. S. Cohen、Lord Todd

  DOI：10.1039/j39660000239

  日期：——

  Dialkyl hydrogen phosphates, RO(R′O)PO2H, are produced from monoalkyl hydrogen phosphonates, RO(HO)PHO, by oxidation either with bromine in pyridine or with carbon tetrachloride and triethylamine with stoicheiometric quantities of an alcohol. In the absence of an alcohol, the former reagent gives sym-dialkyl dihydrogen pyrophosphates in good yield. The nature of the phosphorylating entity in each system

  磷酸二烷基氢酯RO（R'O）PO 2 H由膦酸单烷基氢酯RO（HO）PHO通过在吡啶中的溴或四氯化碳和三乙胺与化学计量的醇氧化而制得。在不存在醇，前者试剂赋予符号二烷基焦磷酸二氢盐以良好的收率。讨论了每个系统中磷酸化实体的性质。
• Composite membrane and method for making the same
  申请人：——

  公开号：US20010050252A1

  公开（公告）日：2001-12-13

  A composite membrane and method for making the same, comprising a porous support and a polyamide surface. The subject membrane provides improved flux and/or rejection rates. The subject membrane is further capable of operating at lower operating pressures. The subject method includes reacting a polyfunctional amine with a polyfunctional acyl halide to form a polyamide. The method includes the step of contacting a complexing agent with the polyfunctional acyl halide prior substantial reaction between the polyfunctional acyl halide and a polyfunctional amine. The subject process is easily adapted to commercial scale manufacturing processes and is particularly suited for making nanofiltration and reverse osmosis composite membranes.

  一种复合膜及其制造方法，包括多孔支架和聚酰胺表面。该膜提高了通量和/或排斥率。该膜还能在较低的工作压力下工作。该方法包括将多官能团胺与多官能团酰基卤反应生成聚酰胺。该方法包括在多官能酰基卤与多官能胺发生实质性反应之前，将络合剂与多官能酰基卤接触。该主题工艺很容易适用于商业规模的制造工艺，尤其适用于制造纳滤和反渗透复合膜。
• QUIN, LOUIS D.;PETE, BELA;SZEWCZYK, JERZY;HUGHES, ALAN N., TETRAHEDRON LETT., 29,(1988) N 22, C. 2627-2630
  作者：QUIN, LOUIS D.、PETE, BELA、SZEWCZYK, JERZY、HUGHES, ALAN N.

  DOI：——

  日期：——