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2,4,5-trichlorophenylhydrazine | 14763-27-0

中文名称
——
中文别名
——
英文名称
2,4,5-trichlorophenylhydrazine
英文别名
(2,4,5-trichloro-phenyl)-hydrazine;(2,4,5-Trichlor-phenyl)-hydrazin;(2,4,5-Trichlorophenyl)hydrazine
2,4,5-trichlorophenylhydrazine化学式
CAS
14763-27-0
化学式
C6H5Cl3N2
mdl
MFCD02656463
分子量
211.478
InChiKey
QFJZMVJDDBTJHB-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:
    132 °C
  • 沸点:
    288.4±40.0 °C(Predicted)
  • 密度:
    1.603±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    38
  • 氢给体数:
    2
  • 氢受体数:
    2

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:
    2,4,5-trichlorophenylhydrazine盐酸 作用下, 生成 2-(2,4,5-trichloro-phenyl)-2H-pyrazole-3,4-dione-4-((Z)-2,4,5-trichloro-phenylhydrazone)
    参考文献:
    名称:
    132. 4:5-二酮吡唑啉的衍生物
    摘要:
    DOI:
    10.1039/jr9320001022
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 盐酸 、 tin(ll) chloride 作用下, 生成 2,4,5-trichlorophenylhydrazine
    参考文献:
    名称:
    CCLXI。—氯对氯取代的azo的作用
    摘要:
    DOI:
    10.1039/jr9310001925
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文献信息

  • Indoleacetic acid derivatives and application thereof as plant growth
    申请人:Nippon Kayaku Kabushiki Kaisha
    公开号:US04806143A1
    公开(公告)日:1989-02-21
    An indole derivative represented by the formula: ##STR1## (wherein each of X.sub.1, X.sub.2 and X.sub.3 is a hydrogen or chlorine atom; X.sub.2 is a chlorine atom and X.sub.3 a hydrogen atom in the case where X.sub.1 is a hydrogen atom; X.sub.2 is a hydrogen atom and X.sub.3 a chlorine atom or a hydrogen atom in the case where X.sub.1 is a chlorine atom; and R.sub.1 is a hydrogen atom, an alkali metal atom, or a lower alkyl group), a plant growth regulator containing said compound as active ingredient, and a method for regulating plant growth which comprises applying said regulator.
    一种以以下结构式表示的吲哚衍生物:##STR1##(其中X.sub.1、X.sub.2和X.sub.3中的每一个是氢原子或氯原子;在X.sub.1为氢原子时,X.sub.2为氯原子,X.sub.3为氢原子;在X.sub.1为氯原子时,X.sub.2为氢原子,X.sub.3为氯原子或氢原子;R.sub.1为氢原子、碱金属原子或较低的烷基基团),一种以该化合物为活性成分的植物生长调节剂,以及一种调节植物生长的方法,包括应用该调节剂。
  • N-phenylpyrazole derivatives
    申请人:MAY & BAKER LIMITED
    公开号:EP0034945A2
    公开(公告)日:1981-09-02
    N-Phenylpyrazole derivatives of the formula:- (wherein each of R5 and R6 represents a C1-C4 alkyl or alkoxy radical, a trifluoromethyl, trifluoromethoxy, nitro, cyano or primary amino radical, or a fluorine, chlorine or bromine atom, each of R', R' and R9 represents a hydrogen atom, a C1-C4 alkyl or alkoxy radical, a trifluoromethyl, trifluoromethoxy, nitro, cyano or primary amino radical or a fluorine, chlorine or bromine atom, or R5, R7, R' and R9 each represents a hydrogen atom and R6 represents a trifluoromethoxy or trifluoromethyl radical, and R10 represents a cyano radical or substituted carbamoyl radical -CONHR", wherein R" represents a methyl or ethyl radical) have been found to possess useful herbicidal properties. All such N-phenylpyrazole derivatives with the exception of 5-amino-4-cyano-1-(2,4-dichlorophenyl)pyrazole and 5-amino-4-cyano-1- (4-chloro-2-methylphenyl)pyrazole are new compounds. Herbicidal compositions containing such N-phenylpyrazole derivatives are described and also processes for the prepararation of the new compounds.
    式中的 N-苯基吡唑衍生物 (其中R5和R6各自代表C1-C4烷基或烷氧基、三氟甲基、三氟甲氧基、硝基、氰基或伯氨基或氟、氯或溴原子,R'、R'和R9各自代表氢原子、C1-C4烷基或烷氧基、三氟甲基、三氟甲氧基、硝基、氰基或伯氨基或氟、R5、R7、R'和 R9 各代表一个氢原子,R6 代表三氟甲氧基或三氟甲基基,R10 代表氰基或取代的氨基甲酰基 -CONHR",其中 R "代表甲基或乙基)已被发现具有有用的除草特性。除 5-氨基-4-氰基-1-(2,4-二氯苯基)吡唑和 5-氨基-4-氰基-1-(4-氯-2-甲基苯基)吡唑外,所有这些 N-苯基吡唑衍生物都是新化合物。本文介绍了含有此类 N-苯基吡唑衍生物的除草组合物,以及制备这些新化合物的工艺。
  • Nalawde, Yogesh Madhukar; Joshi, Vidya, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1998, vol. 37, # 3, p. 310 - 313
    作者:Nalawde, Yogesh Madhukar、Joshi, Vidya
    DOI:——
    日期:——
  • INDOLEACETIC ACID DERIVATIVES AND USE THEREOF AS PLANT GROWTH REGULATORS
    申请人:NIPPON KAYAKU KABUSHIKI KAISHA
    公开号:EP0256128B1
    公开(公告)日:1991-11-06
  • Synthesis and biological evaluation of arylhydrazinocyanoacrylates and N-aryl pyrazolecarboxylates
    作者:Yuxiu Liu、Shaohua Liu、Yonghong Li、Haibin Song、Qingmin Wang
    DOI:10.1016/j.bmcl.2009.04.048
    日期:2009.6
    A series of arylhydrazino-substituted cyanoacrylates 3 and N-aryl pyrazolecarboxylates 6 were synthesized and their bioactivities were evaluated. Though compounds 3 were designed as herbicide, some of them showed fungicidal activity and anti-tumor activity. Some of the compounds 6 exhibited plant growth regulatory activity. (C) 2009 Elsevier Ltd. All rights reserved.
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