1,16-dichloro-hexadecane | 7735-39-9

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 有机氯化物
• 英文名称: 1,16-dichloro-hexadecane
• 英文别名: Hexadecamethylenchlorid；1,16-Dichlor-hexadecan；1,16-Dichlor-eikosan；1,16-Dichlorohexadecane
• CAS: 7735-39-9
• 化学式: C₁₆H₃₂Cl₂
• 分子量: 295.336
• InChiKey: NSSAWKUCPRHLNT-UHFFFAOYSA-N

物化性质

• 熔点：
  47 °C
• 沸点：
  374.1±10.0 °C(Predicted)
• 密度：
  0.936±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  8.3
• 重原子数：
  18
• 可旋转键数：
  15
• 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：
  0

反应信息

• 作为反应物：
  描述：

  1,16-dichloro-hexadecane 在 甲醇 、 三氟化硼乙醚 、 potassium tert-butylate 、 magnesium 作用下， 以 四氢呋喃 为溶剂， 反应 108.0h， 生成
  参考文献：
  名称：

  Preparation of ω-tetrahydropyran-2-ylsulfanylalkylmagnesium chlorides: Useful reagents for the synthesis of 1-(ω-mercaptoalkyl)-1,2-dihydrobuckminsterfullerenes (C60)

  摘要：

  omega-Tetrahydropyran-2-ylsulfanylalkylmagnesium chlorides are prepared as Grignard reagents containing protected mercaptoalkyl chains, which are useful for the direct introduction of omega-mercaptoalkyl chains to electrophiles. In order to prove the usefulness of these reagents, they were reacted with buckminsterfullerene (C(60)) to give 1-(omega-mercaptoalkyl)-1,2-dihydrobuckminsterfullerenes after the deprotection of THP group with TFA. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(98)02142-x
• 作为产物：
  描述：

  11-氯-1-十一碳烯 在 镍 氨 、 氢气 、 溴 、 sodium 、 ferric nitrate 作用下， 以 四氯化碳 、 乙醚 为溶剂， 生成 1,16-dichloro-hexadecane
  参考文献：
  名称：

  Marszak,I. et al., Bulletin de la Societe Chimique de France, 1960, p. 1807 - 1812

  摘要：

  DOI：

文献信息

• The Synthesis of α, ω-Disubstituted Higher Alkanes from α, α, α, ω-Tetrachloroalkanes
  作者：Kazuo Saotome、Hiroshi Komoto、Toshiaki Yamazaki

  DOI：10.1246/bcsj.39.480

  日期：1966.3

  methods of the hydrolysis of α, α, α, ω-tetrachloroalkanes. The reactions were carried out in fuming nitric acid, with the addition of nitrogen dioxide during the reaction or in the presence of a small amount of phosphoric anhydride. α, ω-Dichloroalkanes were derived from the ω-chloroalkanoic acids by the Kolbe electrolytic synthesis. Various other novel α, ω-disubstituted alkanes with very long methylene

  通过改进的 α, α, α, ω-四氯烷烃的水解方法，以良好的产率（超过 90%）制备了比 ω-氯辛酸更高的 ω-氯烷酸。反应在发烟硝酸中进行，在反应过程中加入二氧化氮或在少量磷酸酐的存在下进行。α, ω-二氯烷烃通过 Kolbe 电解合成衍生自 ω-氯代链烷酸。还从四氯烷烃开始制备了各种其他具有很长亚甲基链的新型 α, ω-二取代烷烃，例如二醇、二腈、二羧酸和二胺。
• [EN] SUBSTITUTED AMINO TRIAZOLES USEFUL AS HUMAN CHITINASE INHIBITORS<br/>[FR] TRIAZOLES AMINO-SUBSTITUÉS UTILES EN TANT QU'INHIBITEURS DE CHITINASE HUMAINE
  申请人：ONCOARENDI THERAPEUTICS SP Z O O

  公开号：WO2017037670A1

  公开（公告）日：2017-03-09

  Disclosed are amino triazole compounds substituted with a piperidinyl ring that is itself substituted with a heterocyclic ring. These compounds are inhibitors of acidic mammalian chitinase and chitotriosidase. Also disclosed are methods of using the compounds to treat asthma reactions caused by allergens, as well as acute and chronic inflammatory diseases, autoimmune diseases, dental diseases, neurologic diseases, metabolic diseases, liver diseases, polycystic ovary syndrome, endometriosis, and cancer.

  揭示了一种氨基三唑化合物，其带有一个被杂环环取代的哌啶环。这些化合物是酸性哺乳动物几丁质酶和几丁三糖酶的抑制剂。还公开了使用这些化合物治疗由过敏原引起的哮喘反应，以及急性和慢性炎症性疾病、自身免疫疾病、牙科疾病、神经系统疾病、代谢性疾病、肝脏疾病、多囊卵巢综合征、子宫内膜异位症和癌症的方法。
• [EN] 4, 6-DI (3,12-DIAZA-6, 9-DIAZONIADISPIRO [5.2.5.2] HEXANDECAN-1-YL) -2-METHYL-5-NITROPYRIMIDINE TETRACHLORIDE DIHYDROCHLORIDE HEXAHYDRATE FOR THE TREATMENT OF HERPETIC INFECTION AND A TOPICAL PHARMACEUTICAL COMPOSITION<br/>[FR] HEXAHYDRATE DE DICHLORHYDRATE DE TÉTRACHLORURE DE 4,6-DI(3,12-DIAZA-6,9-DIAZONIADISPIRO[5.2.5.2]HEXADÉCAN-1-YL)-2-MÉTHYL-5-NITROPYRIMIDINE UTILISÉ POUR POUR LE TRAITEMENT DE L'INFECTION HERPÉTIQUE ET COMPOSITION PHARMACEUTIQUE TOPIQUE
  申请人：LTD LIABILITY COMPANY NEARMEDIC PLUS

  公开号：WO2015167368A1

  公开（公告）日：2015-11-05

  The invention relates to the use of 4, 6-di(3,12-diaza-6,9-diazoniadispiro[5.2.5.2]hexadecan-1-yl)-2-methyl-5-nitropyrimidine tetrachloride dihydrochloride hexahydrate exhibiting activity against herpes virus, for the prevention and treatment of herpetic infections in humans and animals by topical administration.

  该发明涉及使用对单核病毒具有活性的4,6-二(3,12-二氮杂-6,9-二氮杂二螺[5.2.5.2]十六烷基)-2-甲基-5-硝基嘧啶四氯化物二盐酸盐六水合物，通过局部给药预防和治疗人类和动物的单纯疱疹感染。
• Process for preparing cationic surface active agents
  申请人：TOHO CHEMICAL INDUSTRY CO., LTD.

  公开号：EP0053389A1

  公开（公告）日：1982-06-09

  A process for preparing specific cationic surface active agents in which nitrogen atoms are attached to both ends of a long-chain alkylene group or polyoxyalkylene group having at least 6-24 carbon atoms in the molecule, at least one of said nitrogen atoms constituting a quaternary ammonium structure, and also at least one hydroxyphenethyl group is bonded to at least one of the two nitrogen atoms. These cationic surface active agents can serve as an accelerator which catalytically promotes changes in a chemical and/or physical change process involving a hydrolyzing, deacidizing or extracting operation using an aqueous solution of an alkaline metal hydroxide or an alkaline earth metal hydroxide.

  一种制备特定阳离子表面活性剂的工艺，其中氮原子连接到分子中至少有 6-24 个碳原子的长链烷基或聚氧亚烷基的两端，所述氮原子中至少有一个构成季铵结构，并且至少有一个羟基苯乙基键合到两个氮原子中的至少一个上。这些阳离子表面活性剂可以作为一种促进剂，在涉及使用碱金属氢氧化物或碱土金属氢氧化物水溶液进行水解、脱酸或萃取操作的化学和/或物理变化过程中催化促进变化。
• Preparation of bis-alpha-keto-carboxylic acids
  申请人：ETHYL CORPORATION

  公开号：EP0142571A1

  公开（公告）日：1985-05-29

  @ A process for preparing bis-α-keto-carboxylic acids by reacting a dihaloalkane in a liquid solvent medium with carbon monoxide at elevated temperature and pressure in the presence of a catalytic amount of a metal carbonyl compound and an alkali or an alkaline earth metal inorganic base.

  一种制备双-α-酮羧酸的工艺，在高温高压下，在催化量的金属羰基化合物和碱金属或碱土金属无机碱的存在下，在液体溶剂介质中使二卤代烷烃与一氧化碳反应。