5-(4-氯苯基)-3-噻二唑-1,2,4-噻二唑 | 74466-94-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 5-(4-氯苯基)-3-噻二唑-1,2,4-噻二唑
• 中文别名: 5-(4-氯苯基)-3-甲基-1,2,4-噻二唑
• 英文名称: 5-(4-Chloro-phenyl)-3-methyl-[1,2,4]thiadiazole
• 英文别名: 5-(4-Chlorophenyl)-3-methyl-1,2,4-thiadiazole
• CAS: 74466-94-7
• 化学式: C₉H₇ClN₂S
• mdl: MFCD00207804
• 分子量: 210.687
• InChiKey: MJDMQQBPPCLSDQ-UHFFFAOYSA-N

物化性质

• 熔点：
  81-83
• 沸点：
  336.9±44.0 °C(Predicted)
• 密度：
  1.326±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.111
• 拓扑面积：
  54
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  4-氯硫代苯甲酰胺 在 2,4,6-三甲基苯磺酰羟胺 作用下， 以 二氯甲烷 为溶剂， 反应 2.02h， 生成 5-(4-氯苯基)-3-噻二唑-1,2,4-噻二唑
  参考文献：
  名称：

  New synthesis of 1,2,4-thiadiazoles

  摘要：

  DOI：

  10.1021/jo01307a006

文献信息

• CARBAMATE DERIVATIVES OF ALKYL-HETEROCYCLES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF
  申请人：Abouabdellah Ahmed

  公开号：US20120015950A1

  公开（公告）日：2012-01-19

  Compound corresponding to general formula (I): in which R 2 is a hydrogen or fluorine atom or a hydroxyl, cyano, trifluoromethyl, C 1-6 -alkyl, C 1-6 -alkoxy or NR 8 R 9 group; n is an integer equal to 1, 2 or 3 and m is an integer equal to 1 or 2; A is a covalent bond or a C 1-8 -alkylene group; R 1 is a phenyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, triazinyl, naphthyl, quinolinyl, isoquinolinyl, phthalazinyl, quinazolinyl, quinoxalinyl, cinnolinyl or naphthyridinyl group, this group being optionally substituted; R 3 is a hydrogen or fluorine atom, a C 1-6 -alkyl group or a tritluoromethyl group; R 4 is a group selected from furanyl, pyrrolyl, thienyl, isothiazolyl, oxazolyl, isoxazolyl, pyrazolyl, oxadiazolyl, thiadiazolyl, imidazole, triazolyl, tetrazolyl, oxazolone, oxazolidinone, isoxazolone, isoxazolidinone, isothiazolone, isothiazolidinone, imidazolone, imidazolidinone, pyrazolone, pyrazolidinone, oxadiazolone, thiadiazolone and triazolone, this group being optionally substituted; in the form of a base or of an addition salt with an acid. Therapeutic use.

  与一般式(I)对应的化合物：其中R2是氢原子或氟原子或羟基、氰基、三氟甲基、C1-6-烷基、C1-6-烷氧基或NR8R9基团；n是等于1、2或3的整数，m是等于1或2的整数；A是共价键或C1-8-烷基烯基团；R1是苯基、吡啶基、吡啉基、嘧啶基、吡嗪基、三嗪基、萘基、喹啉基、异喹啉基、邻苯二嗪基、喹唑啉基、喹喜啉基、喹啉基、咔啉基或萘啉基团，该基团可选择性地被取代；R3是氢原子或氟原子、C1-6-烷基或三氟甲基基团；R4是从呋喃基、吡咯基、噻吩基、异噻唑基、噁唑基、异噁唑基、吡唑基、噁二唑基、噻二唑基、咪唑基、三唑基、四唑基、噁唑酮、噁唑烷酮、异噁唑酮、异噁唑烷酮、异噻唑酮、异噻唑烷酮、咪唑酮、咪唑烷酮、吡唑酮、吡唑烷酮、噁二唑酮、噻二唑酮和三唑酮中选择的基团，该基团可选择性地被取代；以盐酸形式或酸的加合盐形式存在。治疗用途。
• SUBSTITUTED N-HETEROCYCLYL- AND N-HETEROARYL-TETRAHYDROPYRIMIDINONES AND THE SALTS THEREOF, AND THE USE OF SAME AS HERBICIDAL ACTIVE SUBSTANCES
  申请人：Bayer Aktiengesellschaft

  公开号：US20200390100A1

  公开（公告）日：2020-12-17

  The present invention relates to substituted N-heterocyclyl- and N-heteroaryltetrahydropyrimidinones of the general formula (I) or salts thereof, where the radicals in the general formula (I) correspond to the definitions given in the description, and to the use thereof as herbicides, in particular for controlling broad-leaved weeds and/or weed grasses in crops of useful plants and/or as plant growth regulators for influencing the growth of crops of useful plants.

  本发明涉及通式（I）或其盐的取代N-杂环烷基和N-杂芳基四氢嘧啶酮，其中通式（I）中的基团对应于描述中给出的定义，并将其用作除草剂，特别是用于控制作物中的阔叶杂草和/或杂草草，并/或作为植物生长调节剂，以影响作物的生长。
• DERIVES DE CARBAMATES D'ALKYL-HETEROCYCLES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE
  申请人：SANOFI

  公开号：EP2356108A1

  公开（公告）日：2011-08-17
• Small Molecule Sensitization of BAX Activation for Induction of Cell Death
  申请人：Dana-Farber Cancer Institute, Inc.

  公开号：US20200172530A1

  公开（公告）日：2020-06-04

  Provided herein are compositions comprising a compound of Formulas I, II, or III, and compositions a compound comprising a moiety of Formula IV, which are useful for sensitizing and/or activating pro-apoptotic activity of BAX. Methods of treating diseases associated with BAX (e.g., cancer) and methods of identifying compounds which sensitize and/or activate the pro-apoptotic activity of a BAX polypeptide are also provided.
• US8716289B2
  申请人：——

  公开号：US8716289B2

  公开（公告）日：2014-05-06