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2-Brom-1-methoxydecan | 5935-21-7

中文名称
——
中文别名
——
英文名称
2-Brom-1-methoxydecan
英文别名
2-Bromo-1-methoxydecane
2-Brom-1-methoxydecan化学式
CAS
5935-21-7
化学式
C11H23BrO
mdl
——
分子量
251.207
InChiKey
AXLNSDPUFQSDLX-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

物化性质

  • 沸点:
    272.5±13.0 °C(Predicted)
  • 密度:
    1.092±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.9
  • 重原子数:
    13
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:41aae0d8d4f8835ed510b72160aec514
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反应信息

  • 作为产物:
    描述:
    甲醇正癸烯 作用下, 生成 1,2-二溴癸烷 、 1-bromo-2-methoxydecane 、 2-Brom-1-methoxydecan
    参考文献:
    名称:
    Micellar effects on alkene bromination. 2. The role of alkene hydrophobicity
    摘要:
    Surface polarity of cetyltrimethylammonium bromide (CTAB) aqueous micelles was checked by use of as a probe the bromination reaction of a series of 1-alkenes and a water-soluble alkene, cis-4-cyclohexene-1,2-dicarboxylic acid dimethyl ester (I). There was strong inhibition (10(5)-10(6)-fold) of the second-order reaction rate constants relative to those in water; moreover, both kinetics and the product distributions suggested that alkenes had different locations at the micellar surface. Kinetics in the presence of added NaBr and n-decane supported this location hypothesis.
    DOI:
    10.1021/jo00009a019
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文献信息

  • Micellar effects on alkene bromination. 2. The role of alkene hydrophobicity
    作者:Giorgio Cerichelli、Celeste Grande、Luciana Luchetti、Giovanna Mancini
    DOI:10.1021/jo00009a019
    日期:1991.4
    Surface polarity of cetyltrimethylammonium bromide (CTAB) aqueous micelles was checked by use of as a probe the bromination reaction of a series of 1-alkenes and a water-soluble alkene, cis-4-cyclohexene-1,2-dicarboxylic acid dimethyl ester (I). There was strong inhibition (10(5)-10(6)-fold) of the second-order reaction rate constants relative to those in water; moreover, both kinetics and the product distributions suggested that alkenes had different locations at the micellar surface. Kinetics in the presence of added NaBr and n-decane supported this location hypothesis.
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