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methyl 1-methoxy-5-phenyl-2,3,7-trioxabicyclo<2.2.1>hept-5-ene-6-carboxylate | 126835-47-0

中文名称
——
中文别名
——
英文名称
methyl 1-methoxy-5-phenyl-2,3,7-trioxabicyclo<2.2.1>hept-5-ene-6-carboxylate
英文别名
2,3,7-trioxabicyclo<2.2.1>heptene;Methyl 4-methoxy-1-phenyl-2,3,7-trioxabicyclo[2.2.1]hept-5-ene-5-carboxylate
methyl 1-methoxy-5-phenyl-2,3,7-trioxabicyclo<2.2.1>hept-5-ene-6-carboxylate化学式
CAS
126835-47-0
化学式
C13H12O6
mdl
——
分子量
264.235
InChiKey
BCGCLIIWNJLAOQ-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):
    1.1
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    63.2
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    甲醇methyl 1-methoxy-5-phenyl-2,3,7-trioxabicyclo<2.2.1>hept-5-ene-6-carboxylate 反应 3.0h, 以99%的产率得到methyl 4-hydroperoxy-4-methoxy-2-methoxycarbonyl-4-phenylbut-2-enoate
    参考文献:
    名称:
    Iesce, Maria Rosaria; Graziano, Maria Liliana; Cermola, Flavio, Gazzetta Chimica Italiana, 1990, vol. 120, # 10, p. 629 - 635
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    羰基氧化物对电子贫乏烯烃的第一次[3 + 2]环加成反应的区域和立体选择性。1,3-偶极子的双向性
    摘要:
    通过热重排衍生自2,3,7-三恶双环[2.2.1]庚烯(3)的羰基氧化物(1)作为主要产物产生1,2-二氧戊环-4-羧酸甲酯(8)和新型三环双过氧化物(4)(通过X射线衍射确定其结构),分别与丙烯酸甲酯和丙烯酸酯(3)反应,而生成带有乙基乙烯基的5-乙氧基-1,2-二氧戊环(9)醚。
    DOI:
    10.1039/c39890001608
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文献信息

  • Regio- and stereo-selectivity of the first [3 + 2] cycloaddition of carbonyl oxide to electron-poor alkenes. Bidirectionality of the 1,3-dipole
    作者:M. Liliana Graziano、M. Rosaria Iesce、Flavio Cermola、Federico Giordano、Rachele Scarparti
    DOI:10.1039/c39890001608
    日期:——
    The carbonyl oxide (1), derived from the 2,3,7-trioxabicyclo[2.2.1]heptene (3) by thermal rearrangement, yields, as major products, methyl 1,2-dioxolane-4-carboxylate (8) and the novel tricyclic biperoxide (4)(whose structure was established by X-ray diffraction), by reaction with methyl acrylate and the acrylate (3) respectively, whereas it yields 5-ethoxy-1,2-dioxolane (9) with ethyl vinyl ether
    通过热重排衍生自2,3,7-三恶双环[2.2.1]庚烯(3)的羰基氧化物(1)作为主要产物产生1,2-二氧戊环-4-羧酸甲酯(8)和新型三环双过氧化物(4)(通过X射线衍射确定其结构),分别与丙烯酸甲酯和丙烯酸酯(3)反应,而生成带有乙基乙烯基的5-乙氧基-1,2-二氧戊环(9)醚。
  • GRAZIANO, M. LILIANA;IESCE, M. ROSARIA;CERMOLA, FLAVIO;GIORDANO, FEDERICO+, J. CHEM. SOC. CHEM. COMMUN.,(1989) N1, C. 1608-1610
    作者:GRAZIANO, M. LILIANA、IESCE, M. ROSARIA、CERMOLA, FLAVIO、GIORDANO, FEDERICO+
    DOI:——
    日期:——
  • Iesce, M. Rosaria; Cermola, Flavio; Graziano, M. Liliana, Journal of the Chemical Society. Perkin transactions I, 1994, # 1, p. 147 - 152
    作者:Iesce, M. Rosaria、Cermola, Flavio、Graziano, M. Liliana、Scarpati, Rachele
    DOI:——
    日期:——
  • Iesce, Maria Rosaria; Graziano, Maria Liliana; Cermola, Flavio, Gazzetta Chimica Italiana, 1990, vol. 120, # 10, p. 629 - 635
    作者:Iesce, Maria Rosaria、Graziano, Maria Liliana、Cermola, Flavio、Cimminello, Guido、Scaroati, Rachele
    DOI:——
    日期:——
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同类化合物

青蒿氧烷 甲基3-甲基-1,2,4-三氧杂环戊烷-3-羧酸酯 烯丙基苯臭氧化物 5-乙酰基-3,5-二甲基-1,2,4-三氧杂环戊烷-3-甲腈 3-苯基-1,2,4-三氧杂螺[5.4]癸烷 3-甲基-3-苯基-1,2,4-三氧杂螺[5.4]癸烷 3,5-二苯基-1,2,4-三氧杂环戊烷 3,3-二丁基-1,2,4-三氧杂螺[5.4]癸烷 1-异丙基-4-甲基-2,3,7-三氧杂双环[2.2.1]庚烷 1-(5-甲氧基-3-甲基-1,2,4-三四氢呋喃-3-基)乙酮 1-(5,5-二甲基-1,2,4-三四氢呋喃-3-基)乙酮 1-(3,5,5-三甲基-1,2,4-三四氢呋喃-3-基)乙酮 1,2,4-三噁戊环,3-(1-氯乙烯基)- cis-1,4-Dimethyl-2,3,17-trioxabicyclo<12.2.1>heptadecane trans-1,4-Dimethyl-2,3,17-trioxabicyclo<12.2.1>heptadecane adamantane-2-spiro-3'-8'-hydroxy-8'-methyl-1',2',4'-trioxaspiro[4.5]decane adamantane-2-spiro-3'-8'-hydroxy-1',2',4'-trioxaspiro[4.5]decane (3-methyl-1,2,4-trioxolan-3-yl)hexanal (3-methyl-5-phenyl-5-trifluoromethyl-1,2,4-trioxolan-3-yl)pentanal trioxolane 7 3-tert-butyl-3-methyl-5-phenyl-5-trifluoromethyl-1,2,4-trioxolane 3-Cyano-5-cyclohexyl-3-isobutyl-1,2,4-trioxolane 5'-Cyano-5'-isobutylspiro (trans-5-cyano-5-phenyl-1,2,4-trioxolan-3-yl)-3-cyclopentanecarbaldehyde 5'-Cyano-5'-phenylspiro 3-Cyano-3,5-diphenyl-1,2,4-trioxolane 3-Cyano-3-phenyl-5-tert-butyl-1,2,4-trioxolane 3-tert-Butyl-3-methyl-1,2,4-trioxaspiro[5.4]decane (trans-5-cyano-3,5-dimethyl-1,2,4-trioxolan-3-yl)hexanal (trans-5-cyano-5-methyl-1,2,4-trioxolan-3-yl)hexanal 3,5-dimethyl-5-(3-oxopropyl)-1,2,4-trioxolane-3-carbonitrile (trans-5-cyano-5-methyl-1,2,4-trioxolan-3-yl)pentanal 3-Cyano-3-methyl-5-phenyl-1,2,4-trioxolane 3-Cyano-5-cyclohexyl-3-methyl-1,2,4-trioxolane (E)-3-methyl-5-[7-oxohept-5-enyl]-1,2,4-trioxolane-3-carbonitrile (Z)-3-methyl-5-[5-oxopent-1-enyl]-1,2,4-trioxolane-3-carbonitrile (E)-3-methyl-5-[6-oxohex-4-enyl]-1,2,4-trioxolane-3-carbonitrile 3-methyl-5-[(E)-5-oxopent-3-enyl]-1,2,4-trioxolane-3-carbonitrile (Z)-3-methyl-5-[4-methyl-7-oxohept-3-enyl]-1,2,4-trioxolane-3-carbonitrile 3-(Chloromethyl)-3-methoxy-1,2,4-trioxolane cis-3,5-bis-(chloromethyl)-3,5-dimethoxy-1,2,4-trioxolane trans-3,5-bis-(chloromethyl)-3,5-dimethoxy-1,2,4-trioxolane cis-adamantane-2-spiro-3'-8'-[[(4'-formyl-1'-piperazinyl)carbonyl]methyl]-1',2',4'-trioxaspiro[4.5]decane adamantane-2-spiro-3’-8’-hydroxymethyl-1’,2’,4’-trioxaspiro[4,5]decane 3-(Chloromethyl)-3-fluoro-1,2,4-trioxolane trans-3,5-Bis(chloromethyl)-3-fluoro-1,2,4-trioxolane methyl spiro3,7>decane-2,3'-<1,2,4>trioxolane>-5'-carboxylate 3-Cyano-3-phenyl-1,2,4-trioxolane 3-ethyl-1,24-trioxolane dispiro[adamantane-2,2'-[1,3,5]trioxolane-4',1''-cyclohexane]-3''-ol