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dimethyl dibenzosemibullvalene-8b,8d-dicarboxylate | 6580-44-5

中文名称
——
中文别名
——
英文名称
dimethyl dibenzosemibullvalene-8b,8d-dicarboxylate
英文别名
1.2-Dicarbomethoxy-dibenzosemibullvalen;Dimethyl pentacyclo[7.7.0.02,16.03,8.010,15]hexadeca-3,5,7,10,12,14-hexaene-1,2-dicarboxylate
dimethyl dibenzosemibullvalene-8b,8d-dicarboxylate化学式
CAS
6580-44-5
化学式
C20H16O4
mdl
——
分子量
320.345
InChiKey
MXJPMKLCNYRCGS-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

  • 熔点:
    98-99 °C
  • 沸点:
    420.5±45.0 °C(Predicted)
  • 密度:
    1.402±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • Ionic liquid soluble photosensitizers
    作者:Sarah C. Hubbard、Paul B. Jones
    DOI:10.1016/j.tet.2005.05.072
    日期:2005.8
    preparation and investigation of triplet photosensitizers designed to be preferentially soluble in room-temperature ionic liquids are reported. Photosensitizers prepared by covalent attachment of 1-methylimidazole to aryl ketones are soluble in ionic liquids and remain in the ionic liquid layer when the solution is extracted with an organic solvent. The photosensitized isomerization of trans-β-ionol to cis-β-ionol
    报道了设计成优先溶于室温离子液体的三线态光敏剂的制备和研究。通过将1-甲基咪唑共价连接到芳基酮上制备的光敏剂可溶于离子液体,并在用有机溶剂萃取溶液时保留在离子液体层中。在离子液体溶液中有效地进行了反式-β-紫罗兰醇向顺式-β-紫罗兰酚的光敏异构化,提取了产品紫罗兰醇,并将敏化剂/离子液体混合物重新用于其他光敏反应中。讨论了敏化剂在敏化其他反应中的范围和用途。
  • Generation of optical activity through solid state reaction of a racemic mixture that crystallizes in a chiral space group
    作者:Miguel Garcia-Garibay、John R. Scheffer、James Trotter、Fred Wireko
    DOI:10.1016/s0040-4039(00)96626-7
    日期:1987.1
    Because of disorder in the sec-butyl group, the photoreactive isopropyl/(R,S)-sec-butyl diester 3 is able to crystallize as a racemic solid solution in the chiral space group P212121. Irradiation of single crystals of this material leads to products of high optical purity (80% ee). An accompanying process of kinetic resolution leaves the recovered starting material enriched in one of its enantiomers
    由于仲丁基基团的无序性,光反应性异丙基/(R,S)-仲丁基二酯3能够在手性空间基团P2 1 2 1 2 1中结晶为外消旋固溶体。辐照此材料的单晶会产生高光学纯度(ee为80%)的产品。伴随的动力学拆分过程使回收的起始原料富含其一种对映异构体。
  • Sieckmann, Ralf, Journal of Chemical Research, Miniprint, 1994, # 5, p. 1080 - 1090
    作者:Sieckmann, Ralf
    DOI:——
    日期:——
  • Pushing Photochemistry into Water: Acceleration of the Di‐π‐Methane Rearrangement and the Paternó‐Büchi Reaction “On‐Water”
    作者:Robin Schulte、Marco Löcker、Heiko Ihmels、Maximilian Heide、Carsten Engelhard
    DOI:10.1002/chem.202203203
    日期:2023.2.10
    Organic photoreactions “on water”, namely in aqueous suspension or emulsion, are significantly accelerated in this ecologically favorable medium.
    “水上”有机光反应,即在水悬浮液或乳液中,在这种生态有利的介质中显着加速。
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同类化合物

鬼臼酸哌啶基腙氮氧自由基 鬼臼酸 鬼臼毒醇 苦鬼臼毒醇 米托肼 甘尔布林 珠子草次素 消泡剂 愈创木素 异落叶松脂素 异紫杉脂素9,9'-缩丙酮 异紫杉脂素 大侧柏酸 四环[6.6.2.02,7.09,14]十六烷-2(7),3,5,9(14),10,12-己烯-15,15,16,16-四甲腈 叶下珠新素 五脂素A1 7,8,9,9-四去氢异落叶松树脂醇 7,14-二氢-7,14-乙桥二苯并[a,h]蒽-15,16-二羧酸二钠盐 7,14-二氢-7,14-乙桥二苯并[a,h]蒽-15,16-二甲酸 6,8-二溴-4-氧代-4H-1-苯并吡喃-3-甲醛 5a-苯基-5a,14c-二氢苯并[a]茚并[2,1-c]芴-5,10-二酮 1-苯基-1,2,3,4-四氢-萘-2,3-二羧酸 1-(3,4-二羟基苯基)-6,7-二羟基-1,2-二氢萘-2,3-二甲酸 1-(3,4-二甲氧基苯基)-1,2,3,4-四氢-6,7-二甲氧基-2,3-萘二甲醇 1-(3,4-二甲氧基-苯基)-6,7-二甲氧基-1,2,3,4-四氢-萘-2,3-二羧酸 (7S,8S,9R)-9-(3,4-二甲氧基苯基)-6,7,8,9-四氢-4-甲氧基-7,8-双(甲氧基甲基)萘并[1,2-D]-1,3-二恶茂 (7S,8R,9R)-9-(1,3-苯并二氧戊环-5-基)-7,8-二甲基-6,7,8,9-四氢苯并[g][1,3]苯并二氧戊环 (1S,2R,3S)-1-(3,4-二甲氧基苯基)-1,2,3,4-四氢-6,7-二甲氧基-2,3-二甲基-萘 (11S,12R)-9,10-乙桥-9,10-二氢蒽-11,12-二甲酸 (-)-南烛木树脂酚 (+)-异落叶松脂素 (1RS,2SR)-1,2-dihydro-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxynaphthalene-2,3-dicarboxylic acid dimethyl ester (+/-)-(1R,2S,3R)-12-benzyl-4-hydroxy-6,7-methylenedioxy-1-phenyl-2,3,4-trihydrobenzo[f]isoindol-13-one (+/-)-dimethoxy-epi-isopicropodophyllin N-benzyl lactam (+/-)-(1R,2R,3S)-12-benzyl-6,7-methylenedioxy-4-oxo-1-phenyl-2,3-dihydrobenzo[f]isoindol-13-one (+)-ovafolinin B (5R,6R)-methyl 7-(6-fluoro-1H-benzo[d]imidazol-2-yl)-5-(3,4,5-trimethoxyphenyl)-5,6-dihydronaphtho[2,3-d][1,3]dioxole-6-carboxylate 2,5,8-trimethoxy-4a,9,9a,10-tetrahydro-9,10-[1,2]benzenoanthracene-1,4-dione 2,11-dichloro-13b-phenylbenzo[a]indeno[1,2-c]fluorene-9,14(8bH,13bH)-dione rel-(1R,4aR,9S,9aS,10R)-4a,9,9a,10-tetrahydro-9,10-diphenylspiro[9,10-epoxyanthracene-1(4H),2'-oxiran]-4-one 1,4-diphenyl-1,2,3,4-tetrahydro-1,4-epoxido-naphthalene-2,3-dicarboxylic acid diethyl ester rel-(1R,4aS,9R,9aS,10S)-4a,9,9a,10-tetrahydro-9,10-diphenylspiro[9,10-epoxyanthracene-1(4H),2'-oxetane]-4-one endo-2,5-diphenyl-3,4-benzo-14-oxatetracyclo<7.2.2.12,5.01,6>tetradec-3-ene 1a,2,7,7a-tetrahydro-2,7-epoxy-1a-methyl-1,2,7-triphenylbenzonaphthothiophenium triflate endo-2,5-diphenyl-3,4-benzo-14-oxatetracyclo<6.3.2.12,5.01,6>tetradec-3-ene (1S,8R,9S,10S)-1,8-diphenyl-10-methyl-11-oxa-tricyclo[6.2.1.02,7]undeca-2(7),3,5-triene-9-carboxaldegyde 13b-phenylbenzo[a]indeno[1,2-c]fluorene-9,14(8bH,13bH)-dione (1R,2R)-7-methyl-1,2,3-tris(4-methylphenyl)-1,2-dihydronaphthalene methyl 9-deoxy-9-oxo-α-apopicropodophyllate 9-n-hexylimine (15R)-13-(4-fluorophenyl)-10-hydroxy-10,11-dihydro-9H-9,10-[3,4]epipyrroloanthracene-12,14(13H,15H)-dione