m-Fluorobenzyl tert-butyl ether | 72402-80-3

• 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: m-Fluorobenzyl tert-butyl ether
• 英文别名: (3-Fluorophenyl) methanol, tert.-butyl ether；1-fluoro-3-[(2-methylpropan-2-yl)oxymethyl]benzene
• CAS: 72402-80-3
• 化学式: C₁₁H₁₅FO
• 分子量: 182.238
• InChiKey: YOKKPBRMFAVWTQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  13
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  3-氟苄醇 、 叔丁醇 在 硫酸 作用下， 生成 m-Fluorobenzyl tert-butyl ether
  参考文献：
  名称：

  Photochemcial transformations. 26. Sensitized and unsensitized photoreactions of some benzyl chlorides in tert-butyl alcohol

  摘要：

  DOI：

  10.1021/jo01294a007

文献信息

• PROTOZOAN PARASITE GROWTH INHIBITORS
  申请人：Northeastern University

  公开号：US20150259331A1

  公开（公告）日：2015-09-17

  Compounds and methods for inhibiting growth of a protozoan parasite. Methods of treating a protozoan parasite infection in a subject by administering a therapeutically effective amount of a compound as disclosed herein. The compounds and methods can be used to inhibit growth of protozoan parasites such as Trypanosoma brucei, Trypanosoma cruzi, Leishmania spp., and Plasmodium spp.

  用于抑制原生动物寄生虫生长的化合物和方法。通过向主体施用如本文所述的治疗有效量的化合物来治疗原生动物寄生虫感染的方法。这些化合物和方法可用于抑制如非洲锥虫、克鲁兹锥虫、利什曼原虫属和疟原虫属等原生动物寄生虫的生长。
• Piperazine Metabotropic Glutamate Receptor 5 (MGLUR5) Negative Allosteric Modulators For Anxiety/Depression
  申请人：Bursavich Matthew Gregory

  公开号：US20090325964A1

  公开（公告）日：2009-12-31

  The present teachings relate to piperazine metabotropic glutamate receptor 5 (mGluR5) negative allosteric modulators having Formula I: wherein the constituent variables are as defined herein. The present teachings further relate to methods for the preparation of the compounds, and to methods for using the compounds for treatment of diseases and disorders including schizophrenia, paranoia, depression, manic-depressive illness and anxiety.

  本发明涉及具有公式I的哌嗪代谢型谷氨酸受体5（mGluR5）负向变构调节剂： 其中，组成变量如本文所定义。本发明还涉及制备该化合物的方法，并涉及使用该化合物治疗疾病和障碍的方法，包括精神分裂症、偏执症、抑郁症、躁郁病和焦虑症。
• TRIAZINE DERIVATIVES AND THEIR THERAPEUTICAL APPLICATIONS
  申请人：Tao Chunlin

  公开号：US20120172361A1

  公开（公告）日：2012-07-05

  Compounds of the formula (I) and formula (II) and pharmaceutically acceptable salts thereof.

  公式（I）和公式（II）的化合物及其药学上可接受的盐。
• FREDERICAMYCIN DERIVATIVES
  申请人：Abel Ulrich

  公开号：US20120295856A1

  公开（公告）日：2012-11-22

  The invention relates to novel fredericamycin derivatives, to drugs containing said derivatives or the salts thereof, and to the use of the fredericamycin derivatives for treating diseases, especially cancer diseases.

  本发明涉及一种新型的fredericamycin衍生物，以及含有该衍生物或其盐的药物，以及利用该fredericamycin衍生物治疗疾病，特别是癌症疾病的用途。
• Novel Quinazoline Derivatives
  申请人：Zhang Qiang

  公开号：US20130035350A1

  公开（公告）日：2013-02-07

  This disclosure concerns novel quinazoline compounds of Formula (I) as defined in the specification and compositions comprising such novel compounds. These compounds are useful anticancer agents, especially in inhibiting the function of the EGF receptor tyrosine kinases, HER1 tyrosine kinase, and HER2 tyrosine kinase. Thus, the disclosure also concerns a method of treating hyperproliferative diseases or conditions, such as various cancers and benign prostate hyperplasia (BPH), by use of these novel compounds or a composition comprising such novel compounds.

  本公开涉及式（I）中定义的新型喹唑啉化合物及包含这些新型化合物的组合物。这些化合物是有用的抗癌剂，特别是在抑制EGF受体酪氨酸激酶、HER1酪氨酸激酶和HER2酪氨酸激酶的功能方面。因此，本公开还涉及使用这些新型化合物或包含这些新型化合物的组合物治疗过度增殖性疾病或病状，例如各种癌症和良性前列腺增生症（BPH）的方法。