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1-methoxy-3,8-dimethyl-9-xanthenone | 88521-85-1

中文名称
——
中文别名
——
英文名称
1-methoxy-3,8-dimethyl-9-xanthenone
英文别名
1-methoxy-3,8-dimethyl-xanthen-9-one;1-Methoxy-3,8-dimethyl-9H-xanthen-9-one;1-methoxy-3,8-dimethylxanthen-9-one
1-methoxy-3,8-dimethyl-9-xanthenone化学式
CAS
88521-85-1
化学式
C16H14O3
mdl
——
分子量
254.285
InChiKey
VWIJENRXCZYAMA-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):
    3.7
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

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

  • 作为产物:
    参考文献:
    名称:
    Synthetic studies towards the benzophenone precursor for balanol
    摘要:
    Synthesis of 4-carboxy-2,6-dimethoxyphenyl 2'-carboxy-6'-methoxyphenyl ketone, an important precursor for balanol's benzophenone portion, has been achieved via a short and efficient route in three steps using ortho-lithiation as the key step. In another approach aromatization of 2-(2'-methoxy-6'-methylbenzoyl)-5-methyl-1,3-cyclohexanedione afforded benzophenone precursor 2,6-dimethoxy-4-methylphenyl 2'-methoxy-6'-methylphenyl ketone along with the formation of substituted xanthone. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2003.12.029
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文献信息

  • Oxidation of 9-Xanthenones with Lead(IV) Acetate. Formation of Di-γ-lactones
    作者:Hiroshi Nishino、Kazu Kurosawa
    DOI:10.1246/bcsj.56.2847
    日期:1983.9
    The oxidation of 9-xanthenones with lead(IV) acetate afforded 3a,3b,6a,12b-tetrahydro-2H-difuro[3,2-a:3′,2′-c]xanthene-2,5,7(3H,6H)-triones in addition to other products. Characterization of the di-γ-lactones and the difference between the oxidation reaction of lead(IV) and manganese(III) acetates in the 9-xanthenone system are discussed.
    用乙酸铅 (IV) 氧化 9-呫吨酮得到 3a,3b,6a,12b-四氢-2H-二呋喃 [3,2-a:3',2'-c]xanthene-2,5,7(3H ,6H)-triones 以及其他产品。讨论了二-γ-内酯的表征以及 9-呫吨酮系统中乙酸铅 (IV) 和乙酸锰 (III) 的氧化反应之间的差异。
  • Synthetic studies towards the benzophenone precursor for balanol
    作者:Mahesh L Patil、Vishnu H Deshpande、S Ramlingam、Hanumant B Borate
    DOI:10.1016/j.tet.2003.12.029
    日期:2004.2
    Synthesis of 4-carboxy-2,6-dimethoxyphenyl 2'-carboxy-6'-methoxyphenyl ketone, an important precursor for balanol's benzophenone portion, has been achieved via a short and efficient route in three steps using ortho-lithiation as the key step. In another approach aromatization of 2-(2'-methoxy-6'-methylbenzoyl)-5-methyl-1,3-cyclohexanedione afforded benzophenone precursor 2,6-dimethoxy-4-methylphenyl 2'-methoxy-6'-methylphenyl ketone along with the formation of substituted xanthone. (C) 2003 Elsevier Ltd. All rights reserved.
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