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(2,3,4-三氯苯氧基)乙酸 | 25141-27-9

中文名称
(2,3,4-三氯苯氧基)乙酸
中文别名
——
英文名称
2,3,4-trichlorophenoxyacetic acid
英文别名
(2,3,4-Trichlor-phenoxy)-essigsaeure;O-(2.3.4-Trichlor-phenyl)-glykolsaeure;Acetic acid, (2,3,4-trichlorophenoxy)-;2-(2,3,4-trichlorophenoxy)acetic acid
(2,3,4-三氯苯氧基)乙酸化学式
CAS
25141-27-9
化学式
C8H5Cl3O3
mdl
——
分子量
255.485
InChiKey
QMSFHWZMMPPKIR-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

  • 熔点:
    150-160 °C
  • 沸点:
    361.82°C (rough estimate)
  • 密度:
    1.6048 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    3.1
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2918990090

SDS

SDS:786036c071d1da17140e5ef477c31b10
查看

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

点击查看最新优质反应信息

文献信息

  • Novel heterocyclic substituted benzenes, herbicidal compositions containing them and the use thereof for combating weeds
    申请人:ROHM AND HAAS COMPANY
    公开号:EP0068822A2
    公开(公告)日:1983-01-05
    Compounds of the formula below are disclosed as selective herbicides: where W is a substituted heterocyclic selected from: wherein A is O or S: halo is chloro, bromo or fluoro; R1 and R2 are the same or different radicals seiectea from hydrogen or (C1-C4) alkyl; X is hydrogen or halo: X1 is methylene. O or S; Z is carboxy, alkoxyalkoxy, alkoxycarbonyl. alkoxycarbonylalkoxycarbonyl, alkoxyalkoxycarbonyl, acyloxy, acylalkoxy. cyanoalkoxy, alkylthioalkoxy, alkoxycarbonylalkoxy, alkoxycarbonylalkenyloxy, a 5- to 6-membered heterocyclic, formylalkoxy. haloalkoxy, mononuclear arylcarbonyalkoxy, oxiranylalkoxy, ammo. monoalkyl amino. dialkylamino, hydrazino, monoal- kythydrazino, dialkylhydrazino, acyiamino. alkoxyamino, alkoxycarbonylamino, mono- or dialkylcarbonylamino, N-alkyl-N-al- koxyalkylaminocarbonylamino, haloalkylcarbonylamino, N-alkylsulfonylaminocarbonyl, N-alkylsulfonylamino, monoalkenylamino, dialkenylamino, monoalkynylamino, dialkynylamino, N-alkyl-N-alkenylamino, or N-alkyl-N-alkynylamino: R is hydrogen or (C1-C4)alkyl and R3 ana R4 are the same or different and are selected from hydrogen. (C1-C4)-alkyl, (C3-C5)alkenyl or (C3-C5)alkynyl.
    下式化合物被公开为选择性除草剂: 式中 W 是选自下列化合物的取代杂环: 其中 A 是 O 或 S:卤素是氯、溴或氟;R1 和 R2 是由氢或(C1-C4)烷基分离出来的相同或不同的基;X 是氢或卤素:X1 是亚甲基。O或S;Z是羧基、烷氧基烷氧基、烷氧羰基、烷氧羰基烷氧羰基、烷氧烷氧羰基、酰氧基、酰基烷氧基、氰基烷氧基、烷硫基烷氧基、烷氧羰基烷氧基、烷氧羰基烯氧基、5-6元杂环、甲酰基烷氧基、卤代烷氧基、单核烷氧基。单烷基氨基、二烷基氨基、肼基、单醛基肼基、二烷基肼基、酰氨基、烷氧基氨基、烷氧基羰基烷氧基、烷氧基羰基烯氧基、5 至 6 元杂环、甲酰基烷氧基、卤代烷氧基、单核芳基羰基烷氧基、环氧乙烷烷氧基、酰胺。烷氧基氨基、烷氧基羰基氨基、单烷基或二烷基羰基氨基、N-烷基-N-烷氧基烷基氨基羰基氨基、卤代烷基羰基氨基、N-烷基磺酰基氨基羰基、N-烷基磺酰基氨基、单烯基氨基、二烯基氨基、单炔基氨基、二炔基氨基、N-烷基-N-烯基氨基或 N-烷基-N-炔基氨基:R是氢或(C1-C4)烷基,R3和R4相同或不同,选自氢。(C1-C4)-烷基、(C3-C5)烯基或(C3-C5)炔基。
  • Plastic optical fibers and transparent resin used therefor
    申请人:HITACHI, LTD.
    公开号:EP0226020A2
    公开(公告)日:1987-06-24
    A plastic optical fiber comprising a core and a clad, said core being formed by an amorphous and optically transparent polymer and said clad being formed by a polymer having a refractive index lower than that of the core by at least 0.3%, at least one of the core and the clad being formed by an amorphous and optically transparent polymer containing metal elements and halogen atoms, is low in light loss and excellent in heat resistance.
    一种塑料光纤,包括纤芯和包层,所述纤芯由无定形光学透明聚合物形成,所述包层由折射率比纤芯低至少 0.3% 的聚合物形成,纤芯和包层中至少有一个由含有金属元素和卤素原子的无定形光学透明聚合物形成,具有低光损耗和优异的耐热性。
  • Use of xanthine derivatives for host defense mechanism enhancement
    申请人:HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED
    公开号:EP0232438A1
    公开(公告)日:1987-08-19
    The present invention relates to a method of enhancing host defense mechanisms against trauma involving administering to a patient xanthin-derivatives.
    本发明涉及一种增强宿主对创伤的防御机制的方法,包括向患者施用黄嘌呤衍生物。
  • Purine derivatives as interleukin-1 inhibitors
    申请人:HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED
    公开号:EP0279079A2
    公开(公告)日:1988-08-24
    A family of compounds effective in the inhibiting interleukin-1 activity is identified as The inhibition of IL-1 in mammals is implicated in alleviation of a wide variety of diseased conditions.
    抑制哺乳动物体内 IL-1 的活性可减轻多种疾病。
  • Method for evaluating physiological activity of substances and apparatus for the same
    申请人:Inoue, Hiroaki
    公开号:EP0322477A1
    公开(公告)日:1989-07-05
    The method comprises placing test solutions and a buffer solution separately in a cell made of a material that is pervious to laser rays; transmitting a laser beam through each of the solutions in the cell while it is exposed to thermal radiation from an object held at a temperature higher than that of the test solution; measuring expansion of laser beam for measuring degree of fluctuation in liquid structure, by the use of horizontal position of photoreceiver at the rise part of scattering profiles; plotting the relative position of a photoreceiver against the concentration of substance being tested; and evaluating the physiological activity of the substance from the pattern of graph prepared above. An apparatus for evaluating physiological activity is also claimed.
    该方法包括:将测试溶液和缓冲溶液分别放入一个由可透射激光射线的材料制成的池中;在池中的每种溶液暴露于来自温度高于测试溶液温度的物体的热辐射时,发射一束激光;在散射曲线的上升部分利用光接收器的水平位置测量激光束的膨胀,以测量液体结构的波动程度;绘制光接收器的相对位置与被测物质浓度的曲线图;以及根据上述绘制的曲线图评估物质的生理活性。 本发明还要求获得一种评估生理活性的装置。
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