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Dihydro-obscurinervidindiol | 54678-26-1

中文名称
——
中文别名
——
英文名称
Dihydro-obscurinervidindiol
英文别名
15,16-dimethoxy-5'α-methyl-5',6'-dihydro-[1,4]oxazino[4',3',2':1,18,17]aspidospermidine-4β,21-diol;15,16-dimethoxy-22α-methyl-4,25-seco-obscurinervan-4β-ol;(2R,9R,10S,12R,14R,22S)-9-(2-hydroxyethyl)-18,19-dimethoxy-14-methyl-16-oxa-5,13-diazahexacyclo[11.7.1.12,5.02,12.017,21.09,22]docosa-1(20),17(21),18-trien-10-ol
Dihydro-obscurinervidindiol化学式
CAS
54678-26-1
化学式
C24H34N2O5
mdl
——
分子量
430.544
InChiKey
WLXZLUWEEDFULU-DLAGEROHSA-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:
    630.7±55.0 °C(Predicted)
  • 密度:
    1.35±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    31
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    74.6
  • 氢给体数:
    2
  • 氢受体数:
    7

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
  • 下游产品
    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:
    参考文献:
    名称:
    Alkaloid Studies. XLVI.1 The Alkaloids of Aspidosperma obscurinervium Azembuja. A New Class of Heptacyclic Indole Alkaloids2
    摘要:
    DOI:
    10.1021/ja01066a031
  • 作为产物:
    描述:
    (+/-)-obscurinervidine 在 palladium on activated charcoal lithium aluminium tetrahydride 、 氢气 作用下, 以 乙醚乙酸乙酯 为溶剂, 生成 Dihydro-obscurinervidindiol
    参考文献:
    名称:
    Alkaloid Studies. XLVI.1 The Alkaloids of Aspidosperma obscurinervium Azembuja. A New Class of Heptacyclic Indole Alkaloids2
    摘要:
    DOI:
    10.1021/ja01066a031
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文献信息

  • Alkaloid Studies. XLVI.<sup>1</sup> The Alkaloids of <i>Aspidosperma obscurinervium</i> Azembuja. A New Class of Heptacyclic Indole Alkaloids<sup>2</sup>
    作者:Keith S. Brown、Carl. Djerassi
    DOI:10.1021/ja01066a031
    日期:1964.6
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同类化合物

老刺木素 洛柯因 桥替啶 坚木碱 (+/-)-3-oxominovincine (+)-N-methylaspidospermidine Na-formyl-16α-hydroxyaspidospermidine minovincinine (−)-20-epi-pseudocopsinine 14-isovoafoline Voafolin Jerantinine F jerantinine B Jerantinine D (1R,9R,12S,19S)-12-ethyl-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6-trien-10-one Cylindrocarpinol 1-acetyl-2,3-dehydro-8-thioaspidospermidine methyl (1R,9R,10S,12S,19S)-12-ethyl-8,16-diazahexacyclo[10.6.1.01,9.02,7.08,10.016,19]nonadeca-2,4,6-triene-10-carboxylate Dihydrovindoline 10,11-Dibromo 14β-hydroxy-2β,16β-dihydrovincadifformine (2S,3aR,5S,5aS,10bS,12bS)-3a-Ethyl-2,8-dihydroxy-2,3,3a,4,5,5a,6,11,12,12b-decahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-5-carboxylic acid methyl ester 10-nitro vincadifformine 3-oxovincadifformine 8-thioxo-2,3-didehydro-aspidospermidine-3-carboxylic acid methyl ester 11-hydroxyvincadifformine Hazuntiphylline aspidocarpine (-)-jerantinine E 5,17-dioxo-aspidospermidine 5-oxo-aspidospermidine obscurinervidine Dihydro-obscurinervidindiol (-)-aspidosine demethylaspidospermine melodinine K subsessiline Apodine Methyl (1R,12S,20R)-12-ethyl-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6,9-tetraene-10-carboxylate 2,16-dihydrovincadifformine 11-Hydroxy 2β,16β-dihydrovincadifformine 15-nitro-2βH,3βH-vincadifformine 11-Bromo 2β,16β-dihydrovincadifformine (3aS,10bS,11S,12bS)-11-Bromo-3a-ethyl-9-nitro-2,3,3a,4,6,11,12,12b-octahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-5-carboxylic acid methyl ester (3aS,10bS,11S,12bS)-9,11-Dibromo-3a-ethyl-2,3,3a,4,6,11,12,12b-octahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-5-carboxylic acid methyl ester (-)-6S-bromovincadifformine 19-Ethoxycarbonyl-Na-ethyl-19-demethylaspidospermidine (+/-)-12-demethoxy-N-acetylcylindrocarine Na-Acetyl-19-ethoxycarbonyl-19-demethylaspidospermidine rac-methyl (3aR,3a1R,12bS)-3a-(2-ethoxy-2-oxoethyl)-7-ethyl-10,11-dimethoxy-2,3,3a,3a1,7,8,13,14-octahydro-1H,4H-indolizino[8,1-cd][1,4]oxazino[2,3,4-jk]carbazole-5-carboxylate methyl (1S,12R,19R)-12-ethyl-15-oxo-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate