1-Octanaminium, N-ethyl-N,N-dioctyl-, bromide | 40508-21-2

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 1-Octanaminium, N-ethyl-N,N-dioctyl-, bromide
• 英文别名: ethyl(trioctyl)azanium;bromide
• CAS: 40508-21-2
• 化学式: C26H56BrN
• 分子量: 462.6
• InChiKey: ZXSBWHUKLNLVIR-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  5.91
• 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

• METHOD FOR PRODUCING NITROBENZENE COMPOUND
  申请人：Tani Shinki

  公开号：US20140163256A1

  公开（公告）日：2014-06-12

  A method for producing a nitrobenzene compound represented by general formula (2), wherein R 1 and R 5 are the same or different, and each is a halogen atom or another functional group, and R 2 , R 3 , and R 4 are the same or different, and each is a hydrogen atom or another functional group, comprises oxidizing an aniline compound represented by general formula (1), wherein R 1 , R 2 , R 3 , R 4 , and R 5 are the same as described above, with hydrogen peroxide in the presence of a tungsten compound under an acidic condition, followed by oxidation with hydrogen peroxide under a neutral to alkaline condition.

  一种用于制备由通式（2）表示的硝基苯化合物的方法，其中R1和R5相同或不同，每个是卤素原子或另一个官能团，而R2、R3和R4相同或不同，每个是氢原子或另一个官能团，包括在酸性条件下在钨化合物存在下用过氧化氢氧化由通式（1）表示的苯胺化合物，其中R1、R2、R3、R4和R5与上述相同，随后在中性至碱性条件下用过氧化氢氧化。
• METHOD FOR PRODUCING MERCAPTOPHENOL COMPOUND AND INTERMEDIATE OF SAID COMPOUND
  申请人：KUMIAI CHEMICAL INDUSTRY CO., LTD.

  公开号：US20200277257A1

  公开（公告）日：2020-09-03

  A production method in which a mercaptophenol compound is obtained using an industrially preferred sulfur atom introduction reaction, and intermediate compounds of the mercaptophenol compound are provided. A method for producing a mercaptophenol compound in which a phenyl carbamate compound is produced using a phenol compound as a raw material, and then a sulfur atom is regioselectively introduced by a reaction with sulfur monochloride, and a phenyl mercaptocarbamate compound is produced as an intermediate.

  一种生产方法，通过工业上优选的硫原子引入反应获得巯基酚化合物，并提供巯基酚化合物的中间体化合物。一种生产巯基酚化合物的方法，使用苯酚化合物作为原料生产苯基氨甲酸酯化合物，然后通过与硫单氯化物的反应选择性地引入硫原子，产生苯基巯氨甲酸酯化合物作为中间体。
• Process for preparing pyridine-substituted amino ketal derivatives
  申请人：Aventis Pharma Deutschland GmbH

  公开号：US20040158073A1

  公开（公告）日：2004-08-12

  The present invention relates to an efficient process for preparing derivatives of 1-(pyridinyl)-1,1-dialkoxy-2-aminoethane of the formula (I), with which compounds of the formula (I) can be prepared in high purity and yield and in the form of the free base without isolating the acetylpyridine oxime of the formula (XI) which is a critical product from a safety point of view as a solid. 1

  本发明涉及一种高效的方法，用于制备1-(吡啶基)-1,1-二烷氧基-2-氨基乙烷的衍生物，其化合物可以高纯度和高产率地制备，并以游离碱的形式存在，而无需从安全角度考虑的乙酰吡啶肟的固体化合物（化学式（XI））。
• PROCESS FOR PRODUCING POLYVALENT GLYCIDYL COMPOUND
  申请人：SHOWA DENKO K.K.

  公开号：US20170342042A1

  公开（公告）日：2017-11-30

  A polyvalent glycidyl compound is produced from a compound having one or more 2-alkenyl ether groups and two or more 2-alkenyl groups using a hydrogen peroxide aqueous solution as an oxidizing agent to oxidize the 2-alkenyl ether groups and the 2-alkenyl groups. A 2-alkenyl ether compound having two or more (un)substituted 2-alkenyl groups and one or more (un)substituted 2-alkenyl ether groups is oxidized using a hydrogen peroxide aqueous solution as an oxidizing agent in the presence of a tungsten compound and a quaternary ammonium salt as catalysts and of phosphoric acid as a co-catalyst, while controlling the pH of the reaction solution to 1.0-4.0 using an acid other than phosphoric acid. During the oxidation, the step of adding the hydrogen peroxide aqueous solution to the reaction solution and the step of adding the acid other than phosphoric acid thereto are alternately repeated at intervals two or more times.

  使用氢氧化物水溶液作为氧化剂，通过氧化2-烯基醚基团和2-烯基基团，从具有一个或多个2-烯基醚基团和两个或多个2-烯基基团的化合物中产生一种多价环氧化物化合物。在钨化合物和季铵盐作为催化剂和磷酸作为协同催化剂的存在下，在使用氢氧化物水溶液作为氧化剂的同时，氧化具有两个或更多个（未）取代的2-烯基基团和一个或多个（未）取代的2-烯基醚基团的2-烯基醚化合物，并使用除磷酸以外的酸将反应液的pH控制在1.0-4.0之间。在氧化过程中，将氢氧化物水溶液加入反应液和将酸加入其中的步骤交替重复两次或更多次的间隔时间内进行。
• METHOD FOR PRODUCING 1,1,3-TRICHLORO-1-PROPENE
  申请人：Souda Hiroshi

  公开号：US20120142981A1

  公开（公告）日：2012-06-07

  A production method of 1,1,3-trichloro-1-propene comprising the following steps A and B; Step A: 1,1,1,3-tetrachloropropane is dehydrochlorinated at a temperature between 30° C. and 50° C. in the presence of at least one base selected from the group consisting of alkali metal hydroxides and alkaline earth metal hydroxides, and a phase transfer catalyst, Step B: 3,3,3-trichloro-1-propene obtained in the step A is isomerized into 1,1,3-trichloro-1-propene in the presence of a metal catalyst.

  一种制备1,1,3-三氯-1-丙烯的生产方法，包括以下步骤A和B；步骤A：在至少选择自碱金属氢氧化物和碱土金属氢氧化物组成的群体中的至少一种碱基和相转移催化剂的存在下，在30℃至50℃的温度下脱氯化1,1,1,3-四氯丙烷；步骤B：在金属催化剂的存在下将步骤A中获得的3,3,3-三氯-1-丙烯异构化为1,1,3-三氯-1-丙烯。