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3-(2-oxocyclohexyloxy)-8,9,10,11-tetrahydrocyclohepta[c]chromen-6-one | 670245-26-8

中文名称
——
中文别名
——
英文名称
3-(2-oxocyclohexyloxy)-8,9,10,11-tetrahydrocyclohepta[c]chromen-6-one
英文别名
3-[(2-oxocyclohexyl)oxy]-8,9,10,11-tetrahydrocyclohepta[c]chromen-6(7H)-one;3-(2-oxocyclohexyl)oxy-8,9,10,11-tetrahydro-7H-cyclohepta[c]chromen-6-one
3-(2-oxocyclohexyloxy)-8,9,10,11-tetrahydrocyclohepta[c]chromen-6-one化学式
CAS
670245-26-8
化学式
C20H22O4
mdl
——
分子量
326.392
InChiKey
QPCILIIUPIOWGM-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):
    4
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

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:
    3-(2-oxocyclohexyloxy)-8,9,10,11-tetrahydrocyclohepta[c]chromen-6-onesodium hydroxide 作用下, 以 异丙醇 为溶剂, 以86%的产率得到2,3,4,5,10,11,12,13-octahydro[1]benzofuro[3,2-g]cyclohepta[c]chromen-6-one
    参考文献:
    名称:
    Modified coumarins. 24. Synthesis of cycloheptane-annellated tetracyclic furocoumarins
    摘要:
    以2,3,4,5-四氢环庚[c]呋喃[3,2-g]色烯-6-酮为代表的取代物,这类修饰的补骨脂素类似物在呋喃[3,2-g]色烯-7-酮的5,6位置上稠合了一个环庚烷环,是由3-羟基-8,9,10,11-四氢环庚[c]色烯-6-酮合成得到。
    DOI:
    10.1007/s10600-006-0246-8
  • 作为产物:
    描述:
    间苯二酚 在 calcined potash 、 硫酸 作用下, 以 甲醇丙酮 为溶剂, 生成 3-(2-oxocyclohexyloxy)-8,9,10,11-tetrahydrocyclohepta[c]chromen-6-one
    参考文献:
    名称:
    Modified coumarins. 24. Synthesis of cycloheptane-annellated tetracyclic furocoumarins
    摘要:
    以2,3,4,5-四氢环庚[c]呋喃[3,2-g]色烯-6-酮为代表的取代物,这类修饰的补骨脂素类似物在呋喃[3,2-g]色烯-7-酮的5,6位置上稠合了一个环庚烷环,是由3-羟基-8,9,10,11-四氢环庚[c]色烯-6-酮合成得到。
    DOI:
    10.1007/s10600-006-0246-8
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文献信息

  • Modified coumarins. 24. Synthesis of cycloheptane-annellated tetracyclic furocoumarins
    作者:Ya. L. Garazd、M. M. Garazd、A. S. Ogorodniichuk、V. P. Khilya
    DOI:10.1007/s10600-006-0246-8
    日期:2006.11
    Substituted 2,3,4,5-tetrahydrocyclohepta[c]furo[3,2-g]chromen-6-ones, modified psoralen analogs containing a cycloheptane ring annellated to the 5,6-positions of a furo[3,2-g]chromen-7-one, were synthesized from 3-hydroxy-8,9,10,11-tetrahydrocyclohepta[c]chromen-6-ones.
    以2,3,4,5-四氢环庚[c]呋喃[3,2-g]色烯-6-酮为代表的取代物,这类修饰的补骨脂素类似物在呋喃[3,2-g]色烯-7-酮的5,6位置上稠合了一个环庚烷环,是由3-羟基-8,9,10,11-四氢环庚[c]色烯-6-酮合成得到。
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同类化合物

3-羟基-8,9,10,11-四氢-7H-环庚基色烯-6-酮 2-(3,4-亚甲二氧基苯基)环庚三烯并[b]吡喃-4,9-二酮 isobellendine 6,7,8,9-tetrahydro-4-hydroxy-3-(1-phenylpropyl)cycloheptapyran-2(5H)-one isatropolone C 6,8-Dibromo-2-(2-methoxyphenyl)cyclohepta[b]pyran-4,9-dione 13-Amino-11-(4-fluorophenyl)-3,5-dimethyl-7-oxo-4,14-dioxatricyclo[8.4.0.02,6]tetradeca-1(10),2,5,8,12-pentaene-12-carbonitrile 3-Phenyl-4-piperidin-1-yl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyran-2-one 3-Phenyl-4-piperidin-1-yl-6,7-dihydro-5H-1-oxa-dibenzo[a,c]cyclohepten-2-one 4-Morpholin-4-yl-3-phenyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyran-2-one 4-Dimethylamino-3-phenyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyran-2-one 4-Diethylamino-3-phenyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyran-2-one 3-Hydroxy-2-(2-hydroxy-4-methylphenyl)-4,9-dihydrocycloheptapyran-4,9-dione 4-methyl-3-(2-oxopropoxy)-8,9,10,11-tetrahydrocyclohepta[c]chromen-6-one 1,4-Diethyl-6,7,8,9-tetrahydro-5H-cyclohepta[c]pyran-3-one 3-(3,3-dimethyl-2-oxobutoxy)-4-methyl-8,9,10,11-tetrahydrocyclohepta[c]chromen-6-one 2-(3-methoxyphenyl)-4,9-dihydrocyclohepta[b]pyran-4,9-dione 13-oxo-6-phenyl-9-(trifluoromethyl)-6,13-dihydrobenzo[5,6]cyclohepta[1,2-b]chromene-11-carbonitrile N-(2-Oxo-2,5,6,7,8,9-hexahydro-cyclohepta[b]pyran-3-yl)-benzamide N,N-diethyl-13-oxo-6-phenyl-6,13-dihydrobenzo[5,6]cyclohepta[1,2-b]chromene-11-carboxamide 2-Amino-8,10-dimethyl-4-[4-(methylsulfanyl)phenyl]-7-oxo-4H,7H-furo[3',4':6,7]cyclohepta[1,2-B]pyran-3-carbonitrile 2-amino-4-(4-methoxyphenyl)-8,10-dimethyl-7-oxo-4H,7H-furo[3',4':6,7]cyclohepta[1,2-b]pyran-3-carbonitrile 2-amino-4-(4-bromophenyl)-8,10-dimethyl-7-oxo-4H,7H-furo[3',4':6,7]cyclohepta[1,2-b]pyran-3-carbonitrile 2-amino-4-(1,3-benzodioxol-5-yl)-8,10-dimethyl-7-oxo-4H,7H-furo[3',4':6,7]cyclohepta[1,2-b]pyran-3-carbonitrile 2-(Furan-2-yl)cyclohepta[b]pyran-4,9-dione 4-[benzyl(methyl)amino]-3-phenyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyran-2-one 3-(3,3-dimethyl-2-oxobutoxy)-8,9,10,11-tetrahydrocyclohepta[c]chromen-6-one irosustat 6-oxo-6,7,8,9,10,11-hexahydrocyclohepta[c]chromen-3-yl benzenesulfonate 6-oxo-6,7,8,9,10,11-hexahydrocyclohepta[c]chromen-3-yl 4-methylbenzenesulfonate 6-oxo-6,7,8,9,10,11-hexahydrocyclohepta[c]chromen-3-yl methanesulfonate 3-(2-oxopropoxy)-8,9,10,11-tetrahydrocyclohepta[c]chromen-6-one N-methyl-13-oxo-6-phenyl-6,13-dihydrobenzo[5,6]cyclohepta[1,2-b]chromene-11-carboxamide 2-Methyl-9-phenyldibenzo(3,4:6,7)cyclohepta(1,2-b)pyran-4(9H)-one 3-hydroxy-2-propyl-8,9,10,11-tetrahydro-7H-cyclohepta[c]chromen-6-one 3-amino-6,7,8,9-tetrahydrocyclohepta[b]pyran-2(5H)-one 6-oxo-6,7,8,9,10,11-hexahydrocyclohepta[c]chromen-3-yl cyclopropanesulfonate Methyl 4-oxo-3-oxatricyclo[7.2.1.02,7]dodeca-2(7),5-diene-5-carboxylate 13-Amino-11-(2-chlorophenyl)-3,5-dimethyl-7-oxo-4,14-dioxatricyclo[8.4.0.02,6]tetradeca-1(10),2,5,8,12-pentaene-12-carbonitrile 10-methoxy-2,4-dimethylfuro[2',3':3,4]cyclohepta[1,2-c]isochromen-8(6H)-one 4-methyl-3-(2-oxocyclohexyloxy)-8,9,10,11-tetrahydrocyclohepta[c]chromen-6-one 3-(2-oxocyclohexyloxy)-8,9,10,11-tetrahydrocyclohepta[c]chromen-6-one ethyl 13-oxo-6-phenyl-6,13-dihydrobenzo[5,6]cyclohepta[1,2-b]chromene-11-carboxylate 11-bromo-2,4-dimethylfuro[2',3':3,4]cyclohepta[1,2-c]isochromen-8(6H)-one Ethyl 7-cyano-6-ethoxy-3-methyl-5-oxatricyclo[6.4.1.04,13]trideca-1(12),2,4(13),6,8,10-hexaene-2-carboxylate 3-(cyclopropylphenylmethyl)-6,7,8,9-tetrahydro-4-hydroxycycloheptapyran-2(5H)-one Azuleno[1,2-B]oxirene 4,9-Dioxocyclohepta[b]pyran-2-carboxylic acid 8,9-dihydro-7H-5-oxa-benzo[6,7]cyclohepta[1,2-a]naphthalen-6-one 11,12-dimethoxy-8,9-dihydro-7H-5-oxa-benzo[6,7]cyclohepta[1,2-a]naphthalen-6-one