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4-hydroxy-6-methoxy-triazine amine

中文名称
——
中文别名
——
英文名称
4-hydroxy-6-methoxy-triazine amine
英文别名
6-amino-4-methoxy-1H-1,3,5-triazin-2-one
4-hydroxy-6-methoxy-triazine amine化学式
CAS
——
化学式
C4H6N4O2
mdl
——
分子量
142.117
InChiKey
BNRJSGGCKPCNMQ-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):
    -0.8
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    89.1
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    醚黄隆 以 phosphate buffer 为溶剂, 反应 500.0h, 生成 2-氨基-4,6-甲氧基-1,3,5-三嗪4-hydroxy-6-methoxy-triazine amine 、 N'-(4,6-dimethoxy-1,3,5-triazin-2-yl)urea 、 (4,6-Dimethoxy-1,3,5-triazin-2-yl)carbamoylsulfamic acid
    参考文献:
    名称:
    Simulated Sunlight-Induced Photodegradations of Triasulfuron and Cinosulfuron in Aqueous Solutions
    摘要:
    To elucidate the photochemical behavior of two sulfonylureas (cinosulfuron and triasulfuron) for which the chemical formulas are relatively close, their photodegradation was studied in water. All experiments were carried out under laboratory conditions using a xenon arc lamp as the source of radiation to simulate environmental conditions. Polychromatic quantum efficiencies were calculated to determine the photochemical pesticide lifetimes at pH 7, and a comparison with hydrolysis lifetimes has been performed. The results obtained showed clearly that at pH 7, photodegradation becomes a more important pathway than chemical degradation. HPLC-DAD was used to study the kinetics for both sulfonylureas and their photoproducts, whereas HPLC-MS (ESI in positive and negative modes) was used to identify photoproducts. These results suggest that the photodegradation of these two sulfonylureas proceeds via a number of reaction pathways: (1) cleavage of the sulfonylurea bridge; (2) desulfonylation, which can proceed either by a carbon-sulfur cleavage or a nitrogen-sulfur cleavage; (3) O-demethylation of methoxy moieties present on the triazine ring; and (4) O-dealkylation of benzene derivatives. In addition, it was found that the desulfonylation represented the main step and that it was wavelength dependent.
    DOI:
    10.1021/jf010948s
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