乙基三正辛基溴化膦 | 56022-37-8

• 分子结构分类: 有机化合物 - 有机磷化合物 - 四烷基鏻化合物
• 中文名称: 乙基三正辛基溴化膦
• 英文名称: Ethyltrioctylphosphonium bromide
• 英文别名: ethyl(trioctyl)phosphanium;bromide
• CAS: 56022-37-8
• 化学式: C26H56BrP
• 分子量: 479.6
• InChiKey: TUDUDQJRUPFUMA-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  7.11
• 重原子数：
  28
• 可旋转键数：
  22
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  1

文献信息

• Substituted phenyluracils
  申请人：——

  公开号：US20020173425A1

  公开（公告）日：2002-11-21

  Phenyluracils of the general formula (I) 1 in which Q, R 1 , R 2 , R 3 , R 4 , R 5 and R 6 each have one of the meanings given in the description, and processes for their preparation and their use as herbicides.

  通式（I）中的苯基尿嘧啶，其中Q，R1，R2，R3，R4，R5和R6分别具有描述中给出的含义，以及它们的制备过程和用作除草剂的用途。
• SYNTHETIC METHOD FOR THE PREPARATION OF 1, 2-BENZISOTHIAZOLIN-3-ONE
  申请人：Shouguang Syntech Fine Chemical Co., Ltd.

  公开号：US20150336910A1

  公开（公告）日：2015-11-26

  The present invention relates to a method for producing a 1,2-benzisothiazolin-3-one compound (I) by reacting a 2-halobenzonitrile compound (II) with a thiol compound (III) to form an intermediate (IV) and subsequently reacting the intermediate (IV) with a halogenation agent in the presence of water to form a reaction mixture (RM), comprising the 1,2-benzisothiazolin-3-one compound (I) and a halide compound (V).

  本发明涉及一种通过将2-卤代苯腈化合物(II)与硫醇化合物(III)反应以形成中间体(IV)，然后在水的存在下将中间体(IV)与卤代试剂反应以形成反应混合物(RM)，其中包括1,2-苯并异噻唑啉-3-酮化合物(I)和卤化合物(V)的方法。
• Method for Preparing Curable Bicyclic Compound Derived from Biomass
  申请人：Korea Institute of Industrial Technology

  公开号：US20140066637A1

  公开（公告）日：2014-03-06

  The present invention relates to a curable bicyclic compound derived from biomass, solvent-free curable composition and a method for preparing thereof. The curable compound derived from biomass according to the invention comprises a bicycle structure, to which one of two epoxide functional groups are bonded.

  本发明涉及一种来自生物质的可固化的双环化合物，无溶剂可固化组合物以及其制备方法。根据本发明，来自生物质的可固化化合物包括一个双环结构，其中一个或两个环氧基团之一与之结合。
• Substituted iminoazines
  申请人：——

  公开号：US20040029881A1

  公开（公告）日：2004-02-12

  The invention relates to novel substituted iminoazines of the general formula (I) 1 in which R 1 , R 2 , R 3 , R 4 , Z 1 , Z 2 and Z 3 are each as defined in the description, to a plurality of processes and intermediates for their preparation and to their use as herbicides.

  这项发明涉及一种新型的通式（I）中的取代亚胺嘧啶化合物，其中R1、R2、R3、R4、Z1、Z2和Z3分别如描述中所定义，以及它们的制备过程和中间体的多种方法，以及它们作为除草剂的用途。
• [EN] 2-METHYL-THIENO-BENZODIAZEPINE PROCESS<br/>[FR] PROCEDE DE PREPARATION DE 2-METHYL-THIENO-BENZODIAZEPINE
  申请人：WATSON PHARMACEUTICALS INC

  公开号：WO2004094390A1

  公开（公告）日：2004-11-04

  The present invention relates to a novel multistep process for preparing thieno­benzodiazepine derivatives having the following structure (I).

  本发明涉及一种用于制备具有以下结构（I）的噻吩-苯二氮杂环己烯衍生物的新型多步骤工艺。