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1,1-cyclopropanedicarboxaldehyde | 136476-41-0

中文名称
——
中文别名
——
英文名称
1,1-cyclopropanedicarboxaldehyde
英文别名
1,1-cyclopropane dicarboaldehyde;Cyclopropane-1,1-dicarbaldehyde
1,1-cyclopropanedicarboxaldehyde化学式
CAS
136476-41-0
化学式
C5H6O2
mdl
——
分子量
98.1014
InChiKey
LLYSBMNJRGHFBT-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

  • 沸点:
    151.9±23.0 °C(Predicted)
  • 密度:
    1.513±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.3
  • 重原子数:
    7
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1,1-cyclopropanedicarboxaldehyde 在 magnesium sulfate 、 对甲苯磺酸 作用下, 以 乙醇 为溶剂, 反应 1.0h, 生成 1,1-双(二乙氧基甲基)环丙烷1-(二乙氧基甲基)环丙烷甲醛
    参考文献:
    名称:
    Processes for preparation of bicyclic compounds and intermediates therefor
    摘要:
    一种制备中间化合物(VII)、化合物(VIII)和化合物(XIV)的方法,这些化合物将作为合成抗菌化合物的原料,通过化合物(I)或化合物(X)以及化合物(II),每种化合物如下所示;以及用于制备的新化合物。
    公开号:
    US20040019223A1
  • 作为产物:
    描述:
    1,1-环丙基二羧酸吡啶 、 sodium azide 、 硼烷四氢呋喃络合物三丁基膦臭氧 作用下, 以 二甲基亚砜 为溶剂, 反应 34.58h, 生成 1,1-cyclopropanedicarboxaldehyde
    参考文献:
    名称:
    Polynitro-substituted strained-ring compounds. 2. 1,2-Dinitrospiropentanes
    摘要:
    trans-1,2-Dinitrospiropentane was prepared in 43% yield from 1,1-bis(nitromethyl)cyclopropane, best obtained by dry-phase ozonolysis of the corresponding diamine. The structure of trans- 1,2-dinitrospiropentane was assigned on the basis of spectroscopic data, elemental analysis, and X-ray crystallographic data. The first pK(a) was determined to be 18.6-21.6 in DMSO solution with decomposition. Reaction of trans- 1,2-dinitrospiropentane with sodium methoxide and iodine gave a mixture of iodinated spiropentanes, from which, cis- and trans-1,2-diiodo-1,2-dinitrospiropentane could be isolated in pure form. These diiodides were stable at room temperature but gave off iodine upon melting at 150-160-degrees-C. Treatment with sodium thiosulfate in aqueous DMSO solution gave back the deiodinated dinitro compound. trans-1,2-Dinitrospiropentane reacted with lithium diisopropylamide and benzaldehyde in THF to afford a bis(nitroaldol) product in 59% yield.
    DOI:
    10.1021/ja00023a031
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文献信息

  • PROCESSES FOR PREPARATION OF BICYCLIC COMPOUNDS AND INTERMEDIATES THEREFOR
    申请人:DAIICHI PHARMACEUTICAL CO., LTD.
    公开号:EP1310487B1
    公开(公告)日:2007-01-03
  • Processes for preparation of bicyclic compounds and intermediates therefor
    申请人:——
    公开号:US20040019223A1
    公开(公告)日:2004-01-29
    A process for preparing intermediate compound (VII), compound (VIII) and compound (XIV) which will be raw materials for the synthesis of a synthetic antibactrial compound, via compound (I) or compound (X) and then, compound (II), the compounds each being shown below; and novel compounds useful for the preparation. 1
    一种制备中间化合物(VII)、化合物(VIII)和化合物(XIV)的方法,这些化合物将作为合成抗菌化合物的原料,通过化合物(I)或化合物(X)以及化合物(II),每种化合物如下所示;以及用于制备的新化合物。
  • Polynitro-substituted strained-ring compounds. 2. 1,2-Dinitrospiropentanes
    作者:Peter A. Wade、Paul A. Kondracki、Patrick J. Carroll
    DOI:10.1021/ja00023a031
    日期:1991.11
    trans-1,2-Dinitrospiropentane was prepared in 43% yield from 1,1-bis(nitromethyl)cyclopropane, best obtained by dry-phase ozonolysis of the corresponding diamine. The structure of trans- 1,2-dinitrospiropentane was assigned on the basis of spectroscopic data, elemental analysis, and X-ray crystallographic data. The first pK(a) was determined to be 18.6-21.6 in DMSO solution with decomposition. Reaction of trans- 1,2-dinitrospiropentane with sodium methoxide and iodine gave a mixture of iodinated spiropentanes, from which, cis- and trans-1,2-diiodo-1,2-dinitrospiropentane could be isolated in pure form. These diiodides were stable at room temperature but gave off iodine upon melting at 150-160-degrees-C. Treatment with sodium thiosulfate in aqueous DMSO solution gave back the deiodinated dinitro compound. trans-1,2-Dinitrospiropentane reacted with lithium diisopropylamide and benzaldehyde in THF to afford a bis(nitroaldol) product in 59% yield.
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