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cis-2,5-dimethoxybenzo[b]-1,6,6a,12a-tetrahydroxanthone

中文名称
——
中文别名
——
英文名称
cis-2,5-dimethoxybenzo[b]-1,6,6a,12a-tetrahydroxanthone
英文别名
(5aR,11aS)-7,10-dimethoxy-5a,6,11,11a-tetrahydrobenzo[b]xanthen-12-one
cis-2,5-dimethoxybenzo[b]-1,6,6a,12a-tetrahydroxanthone化学式
CAS
——
化学式
C19H18O4
mdl
——
分子量
310.35
InChiKey
FSFKTIZPDWRWTI-KBXCAEBGSA-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):
    3.4
  • 重原子数:
    23
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    New Benzo[ b ]xanthones from Diels-Alder Reactions of Chromone-3-carboxaldehydes with ortho -Benzoquinodimethanes
    摘要:
    New benzo[b]xanthone derivatives, having substituents in the A and D rings, were prepared from cycloaddition reactions of chromone-3-carboxaldehydes with ortho-benzoquinodimethanes, generated in situ from 1,3-dihydrobenzo[c]thiophene 2,2-dioxide, followed by oxidation of the obtained diastereomeric adducts. The structure of all compounds was fully established by 1D and 2D NMR, MS, and elemental analysis. The stereochemistry of the obtained diastereomeric cycloadducts was established by NOESY experiments.
    DOI:
    10.1007/s00706-002-0567-7
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文献信息

  • New Benzo[ b ]xanthones from Diels-Alder Reactions of Chromone-3-carboxaldehydes with ortho -Benzoquinodimethanes
    作者:Angela Sandulache、Artur M. S. Silva、Jos� A. S. Cavaleiro
    DOI:10.1007/s00706-002-0567-7
    日期:2003.3.1
    New benzo[b]xanthone derivatives, having substituents in the A and D rings, were prepared from cycloaddition reactions of chromone-3-carboxaldehydes with ortho-benzoquinodimethanes, generated in situ from 1,3-dihydrobenzo[c]thiophene 2,2-dioxide, followed by oxidation of the obtained diastereomeric adducts. The structure of all compounds was fully established by 1D and 2D NMR, MS, and elemental analysis. The stereochemistry of the obtained diastereomeric cycloadducts was established by NOESY experiments.
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同类化合物

顺式-3,4-二氢-3-(苯基甲基)-2H-1-苯并吡喃-4-醇 表苏木醇 苏木酮A 苏木酚 甲磺酸,三氟-,3,4-二氢-4-羰基-3-(苯基亚甲基)-2H-1-苯并吡喃-7-基酯 甲基麦冬黄酮B SB743921抑制剂 Isobonducellin; (3Z)-2,3-二氢-7-羟基-3-[(4-甲氧基苯基)亚甲基]-4H-1-苯并吡喃-4-酮 9H-占吨-1-羧酸,5-乙酰基-7-[(5-羧基-6,7-二羟基-4-羰基-2H-1-苯并吡喃-3(4H)-亚基)羟甲基]-2,3-二羟基-6-甲基-9-羰基- 8-醛基麦冬高黄酮B 7,3',4'-三羟基-3-苄基-2H-苯并吡喃 4-O-甲基表苏木酚 4-O-甲基蘇木黃素 4'-Demethyl-3,9-dihydroeucomin; 5,7-二羟基-3-(4-羟基苄基)色满-4-酮 3¢-O-甲基苏木醇 3-苯甲酰基-6-硝基-2-苯基-4H-1-苯并吡喃 3-苯甲酰-色酮 3-苄基-4H-1-苯并吡喃-4-酮 3-苄基-2H-色烯 3-p-茴香酰刺槐黄素 3-[(4-羟基苯基)甲基]-2,3-二氢色烯-4-酮 3-(4-羟基苄基)-4H-色烯-4-酮 3-(1,3-苯并二氧戊环-5-基甲基)-5-羟基-7-甲氧基-8-甲基-4-氧代苯并吡喃-6-甲醛 3,4-二氢-4-羟基-3-(苯基甲基)- 2H-1-苯并吡喃-2-酮 3,4-二氢-3-苄基-6-氯甲基香豆素 3'-去氧-4-甲氧基苏木醇 3'-去氧-4-O-甲基表苏木酚 2-甲基-3-(4-硝基苯甲酰基)色酮 2,3-二氢-7-羟基-3-[(4-甲氧基苯基)甲基]-4H-1-苯并吡喃-4-酮 2,3-二氢-5,8-二羟基-3-[(4-羟基苯基)甲基]-7-甲氧基-4H-1-苯并吡喃-4-酮 2,3-二氢-5,7-二羟基-3-[(3-羟基-4-甲氧基苯基)甲基]-4H-1-苯并吡喃-4-酮 1-[(3S,4R)-3-([1,1′-联苯基]-4-基甲基)-3,4-二氢-4-羟基-2H-1-苯并吡喃-7-基]-环戊烷羧酸 (E)-7-羟基-8-甲氧基-3-(4-甲氧基苯亚甲基)色满-4-酮 (6,8-二溴-2-吗啉-4-基-2H-色烯-3-基)(苯基)甲酮 (3E)-8-羟基-7-甲氧基-3-[(4-甲氧基苯基)亚甲基]色满-4-酮 (3E)-7,8-二羟基-3-[(4-甲氧基苯基)亚甲基]色满-4-酮 (3E)-3-[(3,4-二甲氧基苯基)亚甲基]-6-甲氧基色满-4-酮 (3E)-3-(3,4-二甲氧苯亚甲基)-2,3-二氢-4H-色烯-4-酮 (+)-N-((3S,4S)-3-benzyl-4-(4-fluorophenyl)-2-oxo-3,4-dihydro-2H-benzo[h]chromen-3-yl)benzamide 1a,7a-dihydro-7a-(4-methoxybenzoyl)-7H-oxireno<1>benzopyran-4-one 2’,4’-dihydroxyphenyl-5-methoxy-2H-chromen-3-ylmethanone 3-benzoyl-6-methyl-4H-chromen-4-one cis-3,4-dibromo-2,5-dimethoxybenzo[b]-1,6,6a,12a-tetrahydroxanthone cis-2,5-dimethoxybenzo[b]-1,6,6a,12a-tetrahydroxanthone cis-2,5-dimethoxy-10-methylbenzo[b]-1,6,6a,12a-tetrahydroxanthone cis-2,5-dimethoxy-10-chlorobenzo[b]-1,6,6a,12a-tetrahydroxanthone 4-benzoyl-6,8-dibromo-2H-dihydrobenzo[b]pyran-2-spiro-2'-(2',3'-dihydrobenzothiazole) 2,3-dihydro-3-(1-naphthalenylmethylene)-4H-1-benzopyran-4-one 2,3-dihydro-6-methyl-3-(phenylmethylene)-4H-1-benzopyran-4-one 3-[(2-bromophenyl)methylene]-2,3-dihydro-4H-1-benzopyran-4-one