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2,2'-Methylenebis(3,5-dichloro-6-hydroxy-4-methylphenol) | 153444-03-2

中文名称
——
中文别名
——
英文名称
2,2'-Methylenebis(3,5-dichloro-6-hydroxy-4-methylphenol)
英文别名
3,5-dichloro-6-[(2,4-dichloro-5,6-dihydroxy-3-methylphenyl)methyl]-4-methylbenzene-1,2-diol
2,2'-Methylenebis(3,5-dichloro-6-hydroxy-4-methylphenol)化学式
CAS
153444-03-2
化学式
C15H12Cl4O4
mdl
——
分子量
398.07
InChiKey
YQDXOBUVYXEDPQ-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):
    5.33
  • 重原子数:
    23.0
  • 可旋转键数:
    2.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    80.92
  • 氢给体数:
    4.0
  • 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:
    2,2'-Methylenebis(3,5-dichloro-6-hydroxy-4-methylphenol) 生成 3,5-Dichloro-6-(2,4-dichloro-5,6-dihydroxy-3-methyl-benzyl)-4-methyl-[1,2]benzoquinone
    参考文献:
    名称:
    McKague Bruce, Reeve Douglas W., Environ. Sci. and Technol, 28 (1994) N 4, S 573-576
    摘要:
    DOI:
  • 作为产物:
    描述:
    2-甲氧基-4-甲基苯酚sodium hydroxide 、 sodium tetrahydroborate 、 作用下, 以 甲醇 为溶剂, 反应 3.0h, 生成 2,2'-Methylenebis(3,5-dichloro-6-hydroxy-4-methylphenol)
    参考文献:
    名称:
    木质素模型二聚体依次与氯和氢氧化钠反应。
    摘要:
    Dimer 9, which-is;representative of diaryl methane structures reported present in residual lignin, was reacted with aqueous chlorine at 50 degrees C. The major product was identified as the tetrachloroquinone dimer 13 (x = 2, y 2).; Similar reaction of the tetrachlorocatechol dimer 12 with aqueous chlorine gave a mixture of the tetlachloroquinones 15 and 16. When the mixture of the quinones was reacted with 2.5% sodium hydroxide, an intramolecular oxidation-reduction (Cannizzaro) reaction with the simultaneous loss of two chlorine atoms occurred as the main reaction. The products, 21, were characterized as having a chlorine-free muconic acid lactone group attached to a dichlorocatechol. A third product 17 from the reaction with sodium hydroxide appeared to result from simple displacement of the two chlorine atoms in the quinone ring of 15 by hydroxyl groups. The results provide some clarification of the reactions occurring during classical chlorine bleaching. The results are also in agreement with literature reports concerning some of the-structural characteristics of the high mass material.
    DOI:
    10.1021/es00053a007
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