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2,2'-bis[(3-methoxyphenyl)methylene]carbonic dihydrazide

中文名称
——
中文别名
——
英文名称
2,2'-bis[(3-methoxyphenyl)methylene]carbonic dihydrazide
英文别名
1,3-Bis[(3-methoxyphenyl)methylideneamino]urea
2,2'-bis[(3-methoxyphenyl)methylene]carbonic dihydrazide化学式
CAS
——
化学式
C17H18N4O3
mdl
——
分子量
326.355
InChiKey
YHNYTQRIPAKVJC-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):
    2.6
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    84.3
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    碳酰肼3-甲氧基苯甲醛 反应 0.07h, 以97%的产率得到2,2'-bis[(3-methoxyphenyl)methylene]carbonic dihydrazide
    参考文献:
    名称:
    Green Synthetic Method for 1,5‐Disubstituted Carbohydrazones
    摘要:
    A green synthetic method for 1,5-disubstituted carbohydrazones is described. The reaction of dimethyl carbonate with hydrazine hydrate first gave carbohydrazide, which further reacted with various aromatic aldehydes or aliphatic ketones under solvent-free conditions to efficiently afford 1,5-disubstituted carbohydrazone. This protocol has the advantages of using nontoxic dimethyl carbonate as starting material, no use of organic solvents, short reaction time, high yield, and simple workup procedure.
    DOI:
    10.1080/00397910600764600
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文献信息

  • Green Synthetic Method for 1,5‐Disubstituted Carbohydrazones
    作者:Zheng Li、Wei Zhu、Jinlan Yu、Xuelin Ma、Zhong Lu、Shuxiu Xiao
    DOI:10.1080/00397910600764600
    日期:2006.9
    A green synthetic method for 1,5-disubstituted carbohydrazones is described. The reaction of dimethyl carbonate with hydrazine hydrate first gave carbohydrazide, which further reacted with various aromatic aldehydes or aliphatic ketones under solvent-free conditions to efficiently afford 1,5-disubstituted carbohydrazone. This protocol has the advantages of using nontoxic dimethyl carbonate as starting material, no use of organic solvents, short reaction time, high yield, and simple workup procedure.
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