2,3-dimethylthioanisole | 65516-73-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 2,3-dimethylthioanisole
• 英文别名: 1-Methoxy-2,3-bis(methylthio)benzol；1-Methoxy-2,3-bis(methylsulfanyl)benzene
• CAS: 65516-73-6
• 化学式: C₉H₁₂OS₂
• 分子量: 200.326
• InChiKey: SVNGAVJBMVFFIO-UHFFFAOYSA-N

物化性质

• 熔点：
  102-103 °C(Solv: ethanol (64-17-5); water (7732-18-5))
• 沸点：
  273.9±35.0 °C(Predicted)
• 密度：
  1.15±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  12
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  59.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2,3-dimethylthioanisole 在 双氧水 、 溶剂黄146 作用下， 生成 2,3-Bis(methylsulfonyl)anisol
  参考文献：
  名称：

  Nitro displacement by methanethiol anion. Synthesis of bis-, tris-, pentakis-, and hexakis(methylthio)benzenes

  摘要：

  DOI：

  10.1021/jo00404a046
• 作为产物：
  描述：

  甲硫醇 、 2-氯-3-硝基苯甲醚 在 lithium hydroxide 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 2,3-dimethylthioanisole
  参考文献：
  名称：

  Nitro displacement by methanethiol anion. Synthesis of bis-, tris-, pentakis-, and hexakis(methylthio)benzenes

  摘要：

  DOI：

  10.1021/jo00404a046

文献信息

• Insecticidal Benzenedicarboxamide Derivative
  申请人：Wada Katsuaki

  公开号：US20110184188A1

  公开（公告）日：2011-07-28

  The present invention relates to a novel benzenedicarboxamide derivative and the use thereof as an insecticide having the formula (I) wherein the chemical groups W 1 to W 9 , and R 1 to R 3 are as defined here-in.

  本发明涉及一种新型苯二甲酰胺衍生物及其作为杀虫剂的用途，其化学式为(I)，其中化学基团W1至W9，以及R1至R3如本文所定义。
• Method and novel intermediate products for producing isoxazolin-3-yl-acylbenzenenes
  申请人：BASF Aktiengesellschaft

  公开号：US06469176B1

  公开（公告）日：2002-10-22

  The present invention describes a process for preparing isoxazoles of the formula I where: R1 is hydrogen, C1-C6-alkyl, R2 is hydrogen, C1-C6-alkyl, R3, R4, R5 are each hydrogen, C1-C6-alkyl or R4 and R5 together from a bond, R6 is a heterocysclic ring, n is 0, 1 or 2; which comprises preparing an intermediate of the formula VI where R1, R3, R4 and R5 are each as defined above, followed by halogenation, thiomethylation, oxidation and acylation to give compounds of the formula I. Furthermore, the invention describes novel intermediates for preparing the compounds of the formula I and novel processes for preparing the intermediates.

  本发明描述了一种制备式I的异噁唑的过程，其中：R1为氢、C1-C6-烷基，R2为氢、C1-C6-烷基，R3、R4、R5分别为氢、C1-C6-烷基或R4和R5共同形成一个键，R6为杂环环，n为0、1或2；其中包括制备式VI的中间体，其中R1、R3、R4和R5分别如上定义，随后进行卤代、硫甲基化、氧化和酰化以得到式I化合物。此外，该发明描述了制备式I化合物的新中间体和制备这些中间体的新方法。
• Novel compounds having antiinflamatory activity: process for their preparation and pharmaceutical compositions containing them
  申请人：DR. REDDY'S LABORATORIES LTD.

  公开号：US20020032230A1

  公开（公告）日：2002-03-14

  The present invention relates to novel heterocyclic compounds of the general formula (I), their derivatives, their analogs, their tautomeric forms, their stereoisomers, their regioisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates and pharmaceutically acceptable compositions containing them. 1

  本发明涉及一种新型杂环化合物，其一般式为（I），其衍生物，类似物，互变异构体，立体异构体，区域异构体，多晶形态，药学上可接受的盐，药学上可接受的溶剂化合物和药学上可接受的含有它们的组合物。
• Preparation of isoxazolin-3-ylacylbenzenes
  申请人：——

  公开号：US20030018200A1

  公开（公告）日：2003-01-23

  A process is described for preparing isoxazoles of the formula I 1 where the substituents are as defined below: R 1 is hydrogen, C 1 -C 6 -alkyl, R 2 is C 1 -C 6 -alkyl, R 3 , R 4 , R 5 are hydrogen, C 1 -C 6 -alkyl, or R 4 and R 5 together form a bond, R 6 is a heterocyclic ring, n is 0, 1 or 2; which comprises preparing an intermediate of the formula VI 2 where R1, R3, R4 and R5 are as defined above, followed by halogenation, thiomethylation, oxidation and acylation to give compounds of the formula I. Also novel intermediates for preparing the compounds of the formula I and novel processes for preparing the intermediates are described.

  本文描述了一种制备式I1中取代基定义如下的异噁唑的过程： R1为氢、C1-C6烷基， R2为C1-C6烷基， R3、R4、R5为氢、C1-C6烷基，或R4和R5共同形成一个键， R6为杂环环， n为0、1或2； 其中包括制备式VI2的中间体，其中R1、R3、R4和R5如上所定义，随后进行卤代反应、硫甲基化、氧化和酰化，以得到式I的化合物。 还描述了制备式I的新型中间体和制备中间体的新型过程。
• Process and novel intermediates for preparing isoxazolin-3-ylacyl benzenes
  申请人：——

  公开号：US20030028033A1

  公开（公告）日：2003-02-06

  The present invention describes a process for preparing isoxazoles of the formula I 1 where: R 1 is hydrogen, C 1 -C 6 -alkyl, R 2 is hydrogen, C 1 -C 6 -alkyl, R 3 , R 4 , R 5 are each hydrogen, C 1 -C 6 -alkyl or R 4 and R 5 together form a bond, R 6 is a heterocyclic ring, n is 0, 1 or 2; which comprises preparing an intermediate of the formula VI 2 where R 1 , R 3 , R 4 and R 5 are each as defined above, followed by halogenation, thiomethylation, oxidation and acylation to give compounds of the formula I. Furthermore, the invention describes novel intermediates for preparing the compounds of the formula I and novel processes for preparing the intermediates.

  本发明描述了一种制备式I1异构体的过程，其中：R1为氢、C1-C6烷基，R2为氢、C1-C6烷基，R3、R4、R5分别为氢、C1-C6烷基或R4和R5共同形成键，R6为杂环环，n为0、1或2；该过程包括制备式VI2的中间体，其中R1、R3、R4和R5均如上所述，随后进行卤代反应、硫代甲基化、氧化和酰化，以得到式I的化合物。此外，本发明还描述了制备式I化合物的新型中间体和制备中间体的新型过程。