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6-iodo-2-methyl-1-hexene | 134628-15-2

中文名称
——
中文别名
——
英文名称
6-iodo-2-methyl-1-hexene
英文别名
6-iodo-2-methylhex-1-ene
6-iodo-2-methyl-1-hexene化学式
CAS
134628-15-2
化学式
C7H13I
mdl
——
分子量
224.085
InChiKey
RQWBPBHEKOEJBK-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:
    192.3±19.0 °C(Predicted)
  • 密度:
    1.419±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.17
  • 重原子数:
    8.0
  • 可旋转键数:
    4.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

反应信息

  • 作为反应物:
    描述:
    6-iodo-2-methyl-1-hexeneRuCl2(1,3-dimesityl-imidazolidin-2-yl)(PCy3)(=CHPh) sodium hydride 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 1.0h, 生成 (R)-6-methyl-1-aza-10-oxa-bicyclo[6.3.0]undec-6-en-11-one
    参考文献:
    名称:
    Ruthenium Carbene Complexes with N,N‘-Bis(mesityl)imidazol-2-ylidene Ligands:  RCM Catalysts of Extended Scope
    摘要:
    The ruthenium carbene complexes 3a,b bearing imidazol-2-ylidene ligands constitute excellent precatalysts for ring-closing metathesis (RCM) reactions allowing the formation of tri- and tetrasubstituted cycloalkenes. They also apply to annulations that are beyond the scope of the standard Grubbs carbene 1 as well as to ring-closing reactions of acrylic acid derivatives even if the resulting alpha,beta-unsaturated lactones (or lactams) are tri- or tetrasubstituted. The reactivity of 3a was found to be highly dependent on the reaction medium: particularly high reaction rates are observed in toluene, although this solvent also leads to an increased tendency of the catalyst to isomerize the double bonds of the substrates.
    DOI:
    10.1021/jo9918504
  • 作为产物:
    描述:
    5-methyl-5-hexen-1-ol mesylate 在 sodium iodide 作用下, 以 丙酮 为溶剂, 生成 6-iodo-2-methyl-1-hexene
    参考文献:
    名称:
    Bailey, William F.; Khanolkar, Atmaram D.; Gavaskar, Kaustubh, Journal of the American Chemical Society, 1991, vol. 113, # 15, p. 5720 - 5727
    摘要:
    DOI:
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文献信息

  • Synthesis of novel macrocyclic peroxides by bis(sym-collidine)iodine (I) hexafluorophosphate-mediated cyclization of unsaturated hydroperoxides and unsaturated alcohols
    作者:Toyonari Ito、Takahiro Tokuyasu、Araki Masuyama、Masatomo Nojima、Kevin J McCullough
    DOI:10.1016/s0040-4020(02)01556-9
    日期:2003.1
    Bis(sym-collidine)iodine (I) hexafluorophosphate-mediated cyclization of unsaturated hydroperoxides, prepared by a variety of different methods, afforded the corresponding 10- to 20-membered macrocyclic peroxides having two or three peroxide units located within one ring in moderate yields. By analogy, cyclization of unsaturated alcohols having one or two peroxide bond in the chain afforded the corresponding
    通过多种不同方法制备的双(对称-可力丁(I)六氟磷酸酯介导的不饱和氢过氧化物的环化反应,以适中的产率提供了相应的10至20元大环过氧化物,其具有位于一个环内的两个或三个过氧化物单元。类似地,在链中具有一个或两个过氧化物键的不饱和醇的环化得到相应的环醚。发现后者反应的效率是醇结构的函数。
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