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5,6-dibromo-2-methylhex-3-yn-2-ol | 98333-78-9

中文名称
——
中文别名
——
英文名称
5,6-dibromo-2-methylhex-3-yn-2-ol
英文别名
5,6-Dibrom-2-methyl-hex-3-in-2-ol
5,6-dibromo-2-methylhex-3-yn-2-ol化学式
CAS
98333-78-9
化学式
C7H10Br2O
mdl
——
分子量
269.964
InChiKey
PNUSQTPCRNHYSP-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):
    1.7
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

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文献信息

  • Hypohalogenation of vinyl- and allylacetylenes and some chemical transformations of the products
    作者:M. G. Veliev、O. A. Sadygov、Kh. M. Alimardanov、M. I. Shatirova
    DOI:10.1134/s1070428007110036
    日期:2007.11
    Hypohalogenation of 2-methylhex-5-en-3-yn-2-ol, 2-methylhept-6-en-3-yn-2-ol, and their methyl ethers at 303-328 K with hydrochloric or hydrobromic acid in the presence of hydrogen peroxide involves only the double bond to produce the corresponding halohydrins in fairly high yields. Kinetic parameters of these reactions were determined, and the allylacetylenic alcohol and its methyl ether were found to be more reactive than their vinylacetylenic analogs. Acetylenic halohydrins and oxiranes derived therefrom were shown to be quite reactive compounds which may be used as building blocks in organic synthesis.
  • DVORYANCHIKOV, A. I.;ARUTYUNYAN, V. S.;NAM, O MI;KOCHIKYAN, T. V.;ARAKELY+, ARM. XIM. ZH., 41,(1988) N0, S. 619-624
    作者:DVORYANCHIKOV, A. I.、ARUTYUNYAN, V. S.、NAM, O MI、KOCHIKYAN, T. V.、ARAKELY+
    DOI:——
    日期:——
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