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4-methoxy-3,5-dipropylphenol | 141988-98-9

中文名称
——
中文别名
——
英文名称
4-methoxy-3,5-dipropylphenol
英文别名
——
4-methoxy-3,5-dipropylphenol化学式
CAS
141988-98-9
化学式
C13H20O2
mdl
——
分子量
208.301
InChiKey
XUWAQOXYMNEPMJ-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:
    319.7±37.0 °C(Predicted)
  • 密度:
    0.989±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.31
  • 重原子数:
    15.0
  • 可旋转键数:
    5.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    29.46
  • 氢给体数:
    1.0
  • 氢受体数:
    2.0

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:
    甲醇4-methoxy-3,5-dipropylphenolpotassium carbonatethallium(III) nitrate 作用下, 反应 0.17h, 以98%的产率得到4,4-dimethoxy-3,5-dipropyl-2,5-cyclohexadienone
    参考文献:
    名称:
    Photochemistry of Substituted 4,4-Dimethoxy-2,5-Cyclohexadienones
    摘要:
    Abstract4,4‐Dimethoxy‐2,5‐cyclohexadienones 9–14 were prepared from the corresponding hydroquinone monomethyl ethers by oxidation with thallium trinitrate in methanol. Irradiation of solutions of 9–13 in methanol with a broad band of UV light centered at 350 nm in a Rayonet reactor afforded 2‐cyclopentenone derivatives 15–19 in moderate to excellent yields, whereas irradiation of 14 in methanol gave phenol 8 along with other unidentified products. Irradiation of 11–14 in benzene yielded substituted phenols. The plausible reaction pathways for the product formation are discussed.
    DOI:
    10.1002/jccs.199800001
  • 作为产物:
    描述:
    4,4-dimethoxy-3,5-dipropyl-2,5-cyclohexadienone 为溶剂, 反应 6.5h, 以12%的产率得到4-methoxy-3,5-dipropylphenol
    参考文献:
    名称:
    Photochemistry of Substituted 4,4-Dimethoxy-2,5-Cyclohexadienones
    摘要:
    Abstract4,4‐Dimethoxy‐2,5‐cyclohexadienones 9–14 were prepared from the corresponding hydroquinone monomethyl ethers by oxidation with thallium trinitrate in methanol. Irradiation of solutions of 9–13 in methanol with a broad band of UV light centered at 350 nm in a Rayonet reactor afforded 2‐cyclopentenone derivatives 15–19 in moderate to excellent yields, whereas irradiation of 14 in methanol gave phenol 8 along with other unidentified products. Irradiation of 11–14 in benzene yielded substituted phenols. The plausible reaction pathways for the product formation are discussed.
    DOI:
    10.1002/jccs.199800001
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文献信息

  • Photochemistry of Substituted 4,4-Dimethoxy-2,5-Cyclohexadienones
    作者:Fang-Tsao Hong、Kung-Shing Lee、Yow-Fu Tsai、Chun-Chen Liao
    DOI:10.1002/jccs.199800001
    日期:1998.2
    Abstract4,4‐Dimethoxy‐2,5‐cyclohexadienones 9–14 were prepared from the corresponding hydroquinone monomethyl ethers by oxidation with thallium trinitrate in methanol. Irradiation of solutions of 9–13 in methanol with a broad band of UV light centered at 350 nm in a Rayonet reactor afforded 2‐cyclopentenone derivatives 15–19 in moderate to excellent yields, whereas irradiation of 14 in methanol gave phenol 8 along with other unidentified products. Irradiation of 11–14 in benzene yielded substituted phenols. The plausible reaction pathways for the product formation are discussed.
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