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2,4-dichlorophenoxy acetic acid ethylene glycol | 38383-43-6

中文名称
——
中文别名
——
英文名称
2,4-dichlorophenoxy acetic acid ethylene glycol
英文别名
2-Hydroxyethyl 2-(2,4-dichlorophenoxy)acetate
2,4-dichlorophenoxy acetic acid ethylene glycol化学式
CAS
38383-43-6
化学式
C10H10Cl2O4
mdl
——
分子量
265.093
InChiKey
PYRIVSYMXLPCNV-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

物化性质

  • 沸点:
    176-178 °C(Press: 1 Torr)
  • 密度:
    1.3896 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    16
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    55.8
  • 氢给体数:
    1
  • 氢受体数:
    4

SDS

SDS:6306cbdba17ee9ed493b98c6efd884b9
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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
  • 下游产品
    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:
    2,4-dichlorophenoxy acetic acid ethylene glycol硫酸 作用下, 以 为溶剂, 反应 5.0h, 以221 g的产率得到2,4-二氯苯氧乙酸
    参考文献:
    名称:
    一种2,4-二氯苯氧乙酸的制备方法
    摘要:
    本发明提供了一种2,4‑二氯苯氧乙酸的制备方法,包括以下步骤,首先将多元醇和卤代乙酸进行酯化反应,得到卤代乙酸酯;然后将上述步骤得到的卤代乙酸酯与2,4‑二氯酚盐进行反应,得到2,4‑二氯苯氧乙酸酯;最后在复合催化剂的作用下,将上述步骤得到的2,4‑二氯苯氧乙酸酯进行水解反应,得到2,4‑二氯苯氧乙酸和多元醇;所述多元醇为C原子数大于等于2的多元醇。本发明调整工艺路线,从基础上进行创造性改进,该制备方法,工艺简单,条件温和,水解副产物少,产物纯度高,转化率和收率较高,而且中间体卤代乙酸酯稳定,适合大规模工业化生产。
    公开号:
    CN108424365A
  • 作为产物:
    描述:
    2,4-二氯苯氧乙酸乙二醇硫酸 作用下, 反应 2.5h, 以86.8%的产率得到2,4-dichlorophenoxy acetic acid ethylene glycol
    参考文献:
    名称:
    苯并[1,2,3]噻二唑-7-羧酸酯衍生物作为植 物抗病激活剂的应用
    摘要:
    发明涉及式(I)所示的苯并[1,2,3]噻二唑‑7‑羧酸酯衍生物作为植物抗病激活剂的应用。该系列化合物对植物的多种疾病具有一定的防治效果。
    公开号:
    CN102532058B
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文献信息

  • Design, synthesis and herbicidal activities of novel self-dispreading phenoxy carboxylic acid derivatives for the control of water hyacinth floating on the water surface
    作者:Lv-Yin Zheng、Ren-Miao Wu、Wei Guo、Wen-Hua You、Yan-Lan Ling、Xiao-Lin Fan
    DOI:10.1016/j.cclet.2015.04.008
    日期:2015.8
    A series of novel self-dispreading phenoxy carboxylic acid derivatives were designed and synthesized by I-2 catalyzed one-step reaction. Their structures were confirmed by IR, NMR, and HRMS. The derivatives can self-spread and float on the water surface. Preliminary bioassays showed that some compounds, 3i-3p, had excellent herbicidal activities against water hyacinth. This strategy provided a novel approach for the water hyacinth control. (C) 2015 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
  • New Compounds. New Compounds as Plant Growth Regulators
    作者:Melvin Newman、William Fones、Mary Renoll
    DOI:10.1021/ja01195a604
    日期:1947.3
  • Novel Benzo-1,2,3-thiadiazole-7-carboxylate Derivatives As Plant Activators and the Development of Their Agricultural Applications
    作者:Qingshan Du、Weiping Zhu、Zhenjiang Zhao、Xuhong Qian、Yufang Xu
    DOI:10.1021/jf203974p
    日期:2012.1.11
    Plant activators are a novel kind of agrochemicals that could induce resistance in many plants against a broad spectrum of diseases. To date, only few plant activators have been commercialized. In order to develop novel plant activators, a series of benzo-1,2,3-thiadiazole-7-carboxylate derivatives were synthesized, and the structures were characterized by H-1 NMR, IR, elemental analyses, and HRMS or MS. Their potential systemic acquired resistance as plant activators was evaluated as well. Most of them showed good activity, especially, fluoro-containing compounds 3d and 3e, which displayed excellent SAR-inducing activity against cucumber Erysiphe cichoracearum and Colletotrichum lagenarium in assay screening. Field test results illustrated that compounds 3d and 3e were more potent than the commercial plant activator, S-methyl benzo[1,2,3]thiadiazole-7-carbothioate (BTH) toward these pathogens. Further, the preparation of compound 3d is more facile than BTH with lower cost, which will be helpful for further applications in agricultural plant protection.
  • MAMEDOV SH. A.; AXMEDOV V. S., AZEHRB. KIMJA ZH., AZERB. XIM. ZH., 1978, HO 6, 59-65
    作者:MAMEDOV SH. A.、 AXMEDOV V. S.
    DOI:——
    日期:——
  • XYDYROV, D. N.;ALIEV, V. S.;ALIEV, S. M.;PROMONENKOV, V. K.;LIPUSHKINA, N+
    作者:XYDYROV, D. N.、ALIEV, V. S.、ALIEV, S. M.、PROMONENKOV, V. K.、LIPUSHKINA, N+
    DOI:——
    日期:——
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