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14-(tetrahydropyran-2'-yloxy)tetradecan-3-ol | 612069-87-1

中文名称
——
中文别名
——
英文名称
14-(tetrahydropyran-2'-yloxy)tetradecan-3-ol
英文别名
14-(oxan-2-yloxy)tetradecan-3-ol
14-(tetrahydropyran-2'-yloxy)tetradecan-3-ol化学式
CAS
612069-87-1
化学式
C19H38O3
mdl
——
分子量
314.509
InChiKey
JQOUIPACWDFMQQ-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):
    5.2
  • 重原子数:
    22.0
  • 可旋转键数:
    14.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    38.69
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    14-(tetrahydropyran-2'-yloxy)tetradecan-3-ol 在 palladium on activated charcoal 氢气sodium acetatetetra(tert-butyl)ammonium iodide 、 sodium hydride 、 对甲苯磺酸pyridinium chlorochromate 作用下, 以 四氢呋喃甲醇乙醚正己烷二氯甲烷氯仿 为溶剂, 反应 7.0h, 生成 14-hydroxyhexadecanoic acid methyl ester
    参考文献:
    名称:
    Products of Cytochrome P450BioI (CYP107H1)-Catalyzed Oxidation of Fatty Acids
    摘要:
    [GRAPHICS]Oxidation of tetradecanoic and hexadecanoic acids by cytochrome P450(Biol) (CYP107H1) produces mainly the 11-, 12-, and 13-hydroxy C-14 fatty acids and the 11- to 15-hydroxy C-16 fatty acids, respectively. In contrast to previous reports, terminal hydroxylation is not observed. The enantiospecificity of fatty acid hydroxylation by P450(Biol) was also determined, and the enzyme was shown to be moderately selective for production of the (R)-alcohols.
    DOI:
    10.1021/ol035254e
  • 作为产物:
    参考文献:
    名称:
    Products of Cytochrome P450BioI (CYP107H1)-Catalyzed Oxidation of Fatty Acids
    摘要:
    [GRAPHICS]Oxidation of tetradecanoic and hexadecanoic acids by cytochrome P450(Biol) (CYP107H1) produces mainly the 11-, 12-, and 13-hydroxy C-14 fatty acids and the 11- to 15-hydroxy C-16 fatty acids, respectively. In contrast to previous reports, terminal hydroxylation is not observed. The enantiospecificity of fatty acid hydroxylation by P450(Biol) was also determined, and the enzyme was shown to be moderately selective for production of the (R)-alcohols.
    DOI:
    10.1021/ol035254e
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