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octadecane-1,9-diol | 3155-35-9

中文名称
——
中文别名
——
英文名称
octadecane-1,9-diol
英文别名
octadecane-9,1diol;1,9-Dihydroxyoctadecan;Octadecandiol-1,9-diol
octadecane-1,9-diol化学式
CAS
3155-35-9
化学式
C18H38O2
mdl
——
分子量
286.499
InChiKey
GUQPPNZGDSQJGT-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    7
  • 重原子数:
    20
  • 可旋转键数:
    16
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    油酸甲酯 在 lithium aluminium tetrahydride 、 间氯过氧苯甲酸 作用下, 以 乙醚二氯甲烷 为溶剂, 反应 9.0h, 生成 十八烷-1,10-二醇octadecane-1,9-diol
    参考文献:
    名称:
    Organocatalytic synthesis of new telechelic polycarbonates and study of their chemical reactivity
    摘要:
    A two-step versatile process for telechelic polycarbonates synthesis is described. 1-n-butyl-3-methylimidazolium-2-carboxylate (BMIM-2-CO2) was used as thermolabile precursor of N-heterocyclic carbene (NHC) organocatalyst. In a first step, synthesized branched fatty diols or commercially available linear diols were reacted with an excess of dimethylcarbonate (DMC) to afford oligocarbonates with methylcarbonate end-groups. Then, the methylcarbonate groups were reacted with hydroxyl groups of 9-decen-1-ol, 4-hexyn-1-ol and 4-hydroxybenzene ethanol leading to telechelic oligomers with alkene, alkyne and phenol functionalities. Reactivity of these end-groups towards polymerization was successfully evidenced. This procedure could be used for preparing a range of new telechelic oligocarbonates. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.polymer.2015.04.046
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文献信息

  • Process for the preparation of vicinal diols and/or epoxides
    申请人:Solvay Interox GmbH
    公开号:US05344946A1
    公开(公告)日:1994-09-06
    The present invention provides a process for the preparation of vicinal diols and/or epoxides by the oxidation of olefinically-unsaturated compounds with the use of an inorganic heptavalent rhenium compound as catalyst and of hydrogen peroxide as oxidation agent, wherein the reaction is carried out in a solvent selected from the group consisting of organic phosphoric acid esters and ethers with a boiling point above 50.degree. C. under atmospheric conditions.
    本发明提供了一种通过使用无机七价化合物作为催化剂和过氧化氢作为氧化剂,通过氧化烯烃不饱和化合物制备邻二醇和/或环氧化物的方法,其中反应在有机磷酸酯和沸点高于50摄氏度的醚类溶剂中,在大气条件下进行。
  • APPLICATIONS OF BIOBASED GLYCOL COMPOSITIONS
    申请人:Binder Thomas Paul
    公开号:US20080103340A1
    公开(公告)日:2008-05-01
    A biobased replacement for propylene glycol and ethylene glycol derived from petrochemical sources is presented. The product mixture from the hydrogenolysis of certain polyols from biobased renewable resources may replace propylene glycol and ethylene glycol products from petrochemical sources. Applications and methods of the biobased hydrogenolysis product mixture are disclosed. The compositions and methods provide a feedstock for industrial use which has a 13 C/ 12 C isotope ratio characteristic of bioderived material.
    提出了一种基于生物的替代品,用于丙二醇乙二醇,这些替代品源自石化来源。从基于生物可再生资源中的某些多元醇的氢解反应产生的产物混合物可以替代石化来源的丙二醇乙二醇产品。公开了基于生物氢解产物混合物的应用和方法。这些组合物和方法提供了一个13C/12C同位素比特征为生物衍生材料的工业用原料。
  • MONOMERS AND POLYMERS FROM BIODERIVED CARBON
    申请人:Bloom Paul D.
    公开号:US20090018300A1
    公开(公告)日:2009-01-15
    The present disclosure provides compositions including biobased monomers derived from biological sources for the synthesis of polymers from bioderived carbon. The monomers and resulting polymers are comparable to petroleum derived monomers and polymers, but have a carbon isotope ratio characteristic of bioderived materials. Methods for synthesizing polymers having 100% biobased materials are also disclosed.
    本公开提供了包括从生物源获得的生物基单体的组合物,用于从生物衍生碳合成聚合物。这些单体和聚合物与石油衍生的单体和聚合物相似,但具有生物衍生材料的碳同位素比率特征。本公开还揭示了合成100%生物基材料的聚合物的方法。
  • Process for oxidizing primary alcohols
    申请人:——
    公开号:US20020072600A1
    公开(公告)日:2002-06-13
    Primary hydroxyl groups in a substrate having both primary and secondary hydroxyl groups can be selectively oxidized to carbaldehyde and/or carboxyl groups by contacting the substrate with a cyclic nitroxyl compound in the presence of a peroxosulfate as a co-oxidant and by carrying out the reaction at a temperature below 30° C. and at a pH below 9. The process is halogen-free and metal-free and is especially suitable for oxidizing polysaccharides.
    将具有伯羟基和仲羟基的基质与环状硝基化合物接触,在过硫酸盐作为共氧化剂存在下,并在温度低于 30 摄氏度和 pH 值低于 9 的条件下进行反应,可选择性地将基质中的伯羟基氧化成甲醛和/或羧基。该工艺不含卤素和属,尤其适用于氧化多糖
  • Modified polyvinyl alcohol polymers
    申请人:ICI AMERICAS INC.
    公开号:EP0141269B1
    公开(公告)日:1989-08-23
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