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1,3-dimethyl-2-thio-5-(4-methoxybenzyl)barbituric acid | 547726-26-1

中文名称
——
中文别名
——
英文名称
1,3-dimethyl-2-thio-5-(4-methoxybenzyl)barbituric acid
英文别名
——
1,3-dimethyl-2-thio-5-(4-methoxybenzyl)barbituric acid化学式
CAS
547726-26-1
化学式
C14H16N2O3S
mdl
——
分子量
292.359
InChiKey
ZPUOQOVOBUMWAQ-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):
    1.07
  • 重原子数:
    20.0
  • 可旋转键数:
    3.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    49.85
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

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

反应信息

  • 作为反应物:
    描述:
    聚合甲醛cytisine1,3-dimethyl-2-thio-5-(4-methoxybenzyl)barbituric acid乙醇 为溶剂, 反应 6.0h, 以26%的产率得到1,3-dimethyl-2-thio-5-(4-methoxybenzyl)-5-(12-cytisylmethyl)barbituric acid
    参考文献:
    名称:
    摘要:
    The three-dimensional structure of 1,3-dirnethyl-5-(4-allyloxybenzyl)-5-cytisylmethylbarbituric acid was found by x-ray structure analysis. A conformation with proximal cytisine and 2,4,6-trioxopyrimidine moieties was observed. Analogous structures for other synthesized 1,3-dimethyl-5-arylmethyl-5-cytisylmethylbarbituric acids and their 2-thio analogs were proved and the intramolecular effects caused by mutual magnetic shielding of spatially proximal groups were studied using PMR.
    DOI:
    10.1023/a:1022163710687
  • 作为产物:
    描述:
    1,3-二甲基-2-硫代巴比妥酸 在 sodium tetrahydroborate 作用下, 以 乙醇异丙醇 为溶剂, 生成 1,3-dimethyl-2-thio-5-(4-methoxybenzyl)barbituric acid
    参考文献:
    名称:
    摘要:
    The three-dimensional structure of 1,3-dirnethyl-5-(4-allyloxybenzyl)-5-cytisylmethylbarbituric acid was found by x-ray structure analysis. A conformation with proximal cytisine and 2,4,6-trioxopyrimidine moieties was observed. Analogous structures for other synthesized 1,3-dimethyl-5-arylmethyl-5-cytisylmethylbarbituric acids and their 2-thio analogs were proved and the intramolecular effects caused by mutual magnetic shielding of spatially proximal groups were studied using PMR.
    DOI:
    10.1023/a:1022163710687
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