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6-peroxy-7(9)-dehydro-2,3,6,7-tetrahydrogeranyl acetate

中文名称
——
中文别名
——
英文名称
6-peroxy-7(9)-dehydro-2,3,6,7-tetrahydrogeranyl acetate
英文别名
(6-Hydroperoxy-3,7-dimethyloct-7-enyl) acetate;(6-hydroperoxy-3,7-dimethyloct-7-enyl) acetate
6-peroxy-7(9)-dehydro-2,3,6,7-tetrahydrogeranyl acetate化学式
CAS
——
化学式
C12H22O4
mdl
——
分子量
230.304
InChiKey
MHAOGLXADUGTJY-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):
    2.6
  • 重原子数:
    16
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    55.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    乙酸香茅酯 在 bis(dimethyl-di-n-octylammonium) molybdate 、 双氧水 作用下, 以 环己烷 为溶剂, 反应 6.6h, 以66%的产率得到(7-Hydroperoxy-3,7-dimethyloct-5-enyl) acetate
    参考文献:
    名称:
    Synergy between bis(dimethyldioctylammonium) molybdate and tetraethylene glycol monooctyl ether: A winning combination for interfacial catalysis in thermo-controlled and switchable microemulsions
    摘要:
    A simple thermo-responsive one-phase microemulsion (mu em) is designed to enable the dark singlet oxidation of organic substrates while allowing a straightforward separation of the catalytic surfactant and products in two distinct phases by cooling down the reaction medium. This latter is prepared by combining a small amount (1%) of the catalytic surfactant bis(dimethyldioctylammonium) molybdate, [DiC(8)]a[MoO4], with the nonionic amphiphile tetraethylene glycol monooctyl ether, C8E4. Tensiometry and dynamic light scattering are used to rationalize the synergy between the two surfactants which strongly interact. The oxidation takes place in the effective one-phase Winsor IV system which separates into two phases (mu em + oil, i.e. Winsor I) just by temperature change thanks to the presence of the thermosensitive C8E4. The thermal-controlled nanostructured reaction medium is applied to the ene reaction, [4+2] cycloaddition and sulfide oxidation. (C) 2014 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.molcata.2014.11.003
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