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N-[3-yano-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)-sulfinyl]-1H-pyrazol-5-yl]-2-aminoethyl α-D-mannopyranoside

中文名称
——
中文别名
——
英文名称
N-[3-yano-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)-sulfinyl]-1H-pyrazol-5-yl]-2-aminoethyl α-D-mannopyranoside
英文别名
1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(trifluoromethylsulfinyl)-5-[2-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethylamino]pyrazole-3-carbonitrile
N-[3-yano-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)-sulfinyl]-1H-pyrazol-5-yl]-2-aminoethyl α-D-mannopyranoside化学式
CAS
——
化学式
C20H18Cl2F6N4O7S
mdl
——
分子量
643.348
InChiKey
KUWAETJXAXZDGE-NOUYFUIZSA-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):
    2.9
  • 重原子数:
    40
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    189
  • 氢给体数:
    5
  • 氢受体数:
    17

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

  • 作为产物:
    描述:
    氟虫腈 在 sodium tetrahydroborate 、 sodium methylate 、 sodium hydride 、 zinc(II) chloride 作用下, 以 四氢呋喃甲醇二氯甲烷 为溶剂, 反应 6.5h, 生成 N-[3-yano-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)-sulfinyl]-1H-pyrazol-5-yl]-2-aminoethyl β-D-mannopyranoside 、 N-[3-yano-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)-sulfinyl]-1H-pyrazol-5-yl]-2-aminoethyl α-D-mannopyranoside
    参考文献:
    名称:
    Synthesis of a Series of Monosaccharide–Fipronil Conjugates and Their Phloem Mobility
    摘要:
    To test the effect of adding different monosaccharide groups to a non-phloem-mobile insecticide on the phloem mobility of the insecticide, a series of conjugates of different monosaccharides and fipronil were synthesized using the trichloroacetimidate method. Phloem mobility tests in castor bean (Ricinus communis L.) seedlings indicated that the phloem mobility of these conjugates varied markedly. L-Rhamnose fipronil and D-fucose fipronil displayed the highest phloem mobility among all of the tested conjugates. Conjugating hexose, pentose, or deoxysugar to fipronil through an O-glycosidic linkage can confer phloem mobility to fipronil in R. communis L. effectively, while the -OH orientation of the monosaccharide substantially affected the phloem mobility of the conjugates.
    DOI:
    10.1021/jf400888c
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文献信息

  • Synthesis of a Series of Monosaccharide–Fipronil Conjugates and Their Phloem Mobility
    作者:Jian-Guo Yuan、Han-Xiang Wu、Meng-Ling Lu、Gao-Peng Song、Han-Hong Xu
    DOI:10.1021/jf400888c
    日期:2013.5.8
    To test the effect of adding different monosaccharide groups to a non-phloem-mobile insecticide on the phloem mobility of the insecticide, a series of conjugates of different monosaccharides and fipronil were synthesized using the trichloroacetimidate method. Phloem mobility tests in castor bean (Ricinus communis L.) seedlings indicated that the phloem mobility of these conjugates varied markedly. L-Rhamnose fipronil and D-fucose fipronil displayed the highest phloem mobility among all of the tested conjugates. Conjugating hexose, pentose, or deoxysugar to fipronil through an O-glycosidic linkage can confer phloem mobility to fipronil in R. communis L. effectively, while the -OH orientation of the monosaccharide substantially affected the phloem mobility of the conjugates.
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