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(1R,2R,4S)-1,4,5,6-Tetrabromo-7,7-dimethoxy-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid methyl ester | 517876-68-5

中文名称
——
中文别名
——
英文名称
(1R,2R,4S)-1,4,5,6-Tetrabromo-7,7-dimethoxy-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid methyl ester
英文别名
methyl (1R,2R,4S)-1,4,5,6-tetrabromo-7,7-dimethoxybicyclo[2.2.1]hept-5-ene-2-carboxylate
(1R,2R,4S)-1,4,5,6-Tetrabromo-7,7-dimethoxy-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid methyl ester化学式
CAS
517876-68-5
化学式
C11H12Br4O4
mdl
——
分子量
527.83
InChiKey
SGGKMRWYRZIQLL-PDFZIDOMSA-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):
    2.2
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    (1R,2R,4S)-1,4,5,6-Tetrabromo-7,7-dimethoxy-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid methyl ester 在 lithium aluminium tetrahydride 作用下, 以 乙醚 为溶剂, 反应 4.0h, 生成 ((1R,2R,4S)-1,4,5,6-Tetrabromo-7,7-dimethoxy-bicyclo[2.2.1]hept-5-en-2-yl)-methanol
    参考文献:
    名称:
    摘要:
    Effect of the conditions on the enantiomeric purity, overall yield, and isomeric composition of chiral polybromonorbornene Diels-Alder adducts of polybromocyclopentadienes and (-)-menthyl acrylate was studied. Enantiomerically pure polybromonorbornenecarboxylic acids were obtained by resolution of the corresponding racemates through diastereoisomeric salts with l-ephedrine. The structure of the products was confirmed by the IR and H-1 NMR spectra.
    DOI:
    10.1023/a:1015386221273
  • 作为产物:
    描述:
    (-)-menthyl 1,2,3,4-tetrabromo-7,7-dimethoxybicyclo[2.2.1]hept-2-ene-5-carboxylate 在 氢氧化钾 作用下, 以 乙醚乙醇 为溶剂, 反应 2.5h, 生成 (1R,2R,4S)-1,4,5,6-Tetrabromo-7,7-dimethoxy-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid methyl ester
    参考文献:
    名称:
    摘要:
    Effect of the conditions on the enantiomeric purity, overall yield, and isomeric composition of chiral polybromonorbornene Diels-Alder adducts of polybromocyclopentadienes and (-)-menthyl acrylate was studied. Enantiomerically pure polybromonorbornenecarboxylic acids were obtained by resolution of the corresponding racemates through diastereoisomeric salts with l-ephedrine. The structure of the products was confirmed by the IR and H-1 NMR spectra.
    DOI:
    10.1023/a:1015386221273
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文献信息

  • MUSTAFAEV, A. M.;IMAMALIEV, A. B.;GUSEJNOV, M. M., ZH. ORGAN. XIMII, 25,(1989) N, S. 1908-1915
    作者:MUSTAFAEV, A. M.、IMAMALIEV, A. B.、GUSEJNOV, M. M.
    DOI:——
    日期:——
  • ——
    作者:E. G. Mamedov
    DOI:10.1023/a:1015386221273
    日期:——
    Effect of the conditions on the enantiomeric purity, overall yield, and isomeric composition of chiral polybromonorbornene Diels-Alder adducts of polybromocyclopentadienes and (-)-menthyl acrylate was studied. Enantiomerically pure polybromonorbornenecarboxylic acids were obtained by resolution of the corresponding racemates through diastereoisomeric salts with l-ephedrine. The structure of the products was confirmed by the IR and H-1 NMR spectra.
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