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2-(Furan-2-ylmethyl)-3-methylcyclohex-2-en-1-one | 188200-32-0

中文名称
——
中文别名
——
英文名称
2-(Furan-2-ylmethyl)-3-methylcyclohex-2-en-1-one
英文别名
——
2-(Furan-2-ylmethyl)-3-methylcyclohex-2-en-1-one化学式
CAS
188200-32-0
化学式
C12H14O2
mdl
——
分子量
190.242
InChiKey
HKMARDDMIMOEPK-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:
    308.9±31.0 °C(Predicted)
  • 密度:
    1.097±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    30.2
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-(Furan-2-ylmethyl)-3-methylcyclohex-2-en-1-one六甲基磷酰三胺氢氧化钾三氟乙酸酐 作用下, 以 三氟乙酸 为溶剂, 反应 107.0h, 生成
    参考文献:
    名称:
    Synthetic studies towards furosesquiterpenes: Construction of linearly-fused trans- and cis-furo[3,2-b]-and furo[2,3-b] decalins
    摘要:
    Linearly fused furo[2.3-b]- and furo[3,2-b] decalin systems with cis trans ring junctions are present in several furosesquiterpenes obtained from marine sponges. A short and efficient synthesis of this ring system is described starting from Hageman's ester (1). The method has been extended for the synthesis of compound 8 and 14 via the diketones 5,6 and 12 respectively. (C) 1997 Published by Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4020(97)00053-7
  • 作为产物:
    描述:
    糠基氯氢氧化钾potassium tert-butylate 作用下, 以 乙醇叔丁醇 为溶剂, 反应 14.0h, 生成 2-(Furan-2-ylmethyl)-3-methylcyclohex-2-en-1-one
    参考文献:
    名称:
    Synthetic studies towards furosesquiterpenes: Construction of linearly-fused trans- and cis-furo[3,2-b]-and furo[2,3-b] decalins
    摘要:
    Linearly fused furo[2.3-b]- and furo[3,2-b] decalin systems with cis trans ring junctions are present in several furosesquiterpenes obtained from marine sponges. A short and efficient synthesis of this ring system is described starting from Hageman's ester (1). The method has been extended for the synthesis of compound 8 and 14 via the diketones 5,6 and 12 respectively. (C) 1997 Published by Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4020(97)00053-7
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文献信息

  • Synthetic studies towards furosesquiterpenes: Construction of linearly-fused trans- and cis-furo[3,2-b]-and furo[2,3-b] decalins
    作者:Arindam Chakraborty、Gandhi K. Kar、Jayanta K. Ray
    DOI:10.1016/s0040-4020(97)00053-7
    日期:1997.2
    Linearly fused furo[2.3-b]- and furo[3,2-b] decalin systems with cis trans ring junctions are present in several furosesquiterpenes obtained from marine sponges. A short and efficient synthesis of this ring system is described starting from Hageman's ester (1). The method has been extended for the synthesis of compound 8 and 14 via the diketones 5,6 and 12 respectively. (C) 1997 Published by Elsevier Science Ltd.
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