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1,1,2,2,2-pentachloroethanol

中文名称
——
中文别名
——
英文名称
1,1,2,2,2-pentachloroethanol
英文别名
——
1,1,2,2,2-pentachloroethanol化学式
CAS
——
化学式
C2HCl5O
mdl
——
分子量
218.294
InChiKey
GNHASCMMTAHAAH-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):
    2.7
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Spectroscopic and Dielcometric Study of the Kinetics of Alcoholysis of Trichloroacetyl Chloride with Butanol
    摘要:
    The kinetics of alcoholysis of trichloroacetyl chloride with butanol in carbon tetrachloride were studied by dielcometry and IR spectroscopy. The reaction is reversible, and it involves intermediate formation of 1-butoxy-1,2,2,2-tetrachloroethanol and 1,1,2,2,2-pentachloroethanol.
    DOI:
    10.1023/b:rugc.0000018658.61663.42
  • 作为产物:
    描述:
    三氯乙酰氯盐酸 作用下, 以 四氯化碳 为溶剂, 生成 1,1,2,2,2-pentachloroethanol
    参考文献:
    名称:
    Spectroscopic and Dielcometric Study of the Kinetics of Alcoholysis of Trichloroacetyl Chloride with Butanol
    摘要:
    The kinetics of alcoholysis of trichloroacetyl chloride with butanol in carbon tetrachloride were studied by dielcometry and IR spectroscopy. The reaction is reversible, and it involves intermediate formation of 1-butoxy-1,2,2,2-tetrachloroethanol and 1,1,2,2,2-pentachloroethanol.
    DOI:
    10.1023/b:rugc.0000018658.61663.42
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文献信息

  • TETRAZOLINONE COMPOUND AND USE OF SAME
    申请人:SUMITOMO CHEMICAL COMPANY, LIMITED
    公开号:US20160081339A1
    公开(公告)日:2016-03-24
    A tetrazolinone compound of formula (1): wherein R 1 and R 2 each independently represents a hydrogen atom, etc.; R 3 represents a C1-C6 alkyl group, etc.; R 4 , R 5 , and R 6 each independently represents a hydrogen atom, etc.; A represents a C6-C16 aryl group optionally having one or more atoms or groups selected from Group P, etc.; Q represents the following group Q1, etc.; and X represents an oxygen atom or a sulfur atom, has excellent control activity against pests.
    一种化学式(1)所示的四唑酮化合物: 其中R1和R2分别独立表示氢原子,等等; R3表示C1-C6烷基,等等;R4、R5和R6分别独立表示氢原子,等等;A表示一个C6-C16芳基,可选地具有来自P族等组的一个或多个原子或基团;Q表示以下Q1组等;以及 X表示氧原子或硫原子,对害虫具有出色的控制活性。
  • [EN] TETRAZOLINONE COMPOUNDS AND ITS USE AS PESTICIDES<br/>[FR] COMPOSÉS DE TÉTRAZOLINONE ET LEUR UTILISATION EN TANT QUE PESTICIDES
    申请人:SUMITOMO CHEMICAL CO
    公开号:WO2013162072A1
    公开(公告)日:2013-10-31
    The present invention provides a compound having an excellent efficacy for controlling pests. A tetrazolinone compound of a formula (1): [wherein R1 represents an C6-C16 aryl group, an C1-C12 alkyl group, or a C3-C12 cycloalkyl group, etc., which each optionally be substituted; R2, R3, R4 and R5 represent independently of each other a hydrogen atom, a halogen atom or an C1-C3 alkyl group, etc.; R6 represents an C1-C6 alkyl group, a C3-C6 cycloalkyl group, a halogen atom, a C1-C6 haloalkyl group, an C2-C6 alkenyl group, an C1-C6 alkoxy group, or a C1-C6 haloalkoxy group, etc.; R7, R8 and R9 represent independently of each other a hydrogen atom, a halogen atom, or an C1-C4 alkyl group, etc.; X represents an oxygen atom or a sulfur atom; and R10 represents an C1-C6 alkyl group, etc.] shows an excellent controlling efficacy on pests.
    本发明提供了一种具有优异杀虫效果的化合物。公式(1)的四唑酮化合物:[其中R1代表C6-C16芳基、C1-C12烷基或C3-C12环烷基等,每个都可以选择性地被取代;R2、R3、R4和R5分别独立地代表氢原子、卤素原子或C1-C3烷基等;R6代表C1-C6烷基、C3-C6环烷基、卤素原子、C1-C6卤代烷基、C2-C6烯基、C1-C6烷氧基或C1-C6卤代烷氧基等;R7、R8和R9分别独立地代表氢原子、卤素原子或C1-C4烷基等;X代表氧原子或硫原子;R10代表C1-C6烷基等]在杀虫方面表现出优异的控制效果。
  • Process for the preparation of alpha-aminosubstituted carboxylic acid amides
    申请人:——
    公开号:US20040034250A1
    公开(公告)日:2004-02-19
    The invention relates to a process for the preparation of &agr;-aminosubstituted carboxylic acid amide compounds and/or their salts comprising reacting a carboxylic acid amide of a primary amine with a nitrosylating agent in the presence of a base followed by hydrolysis to give a hydroxy imino derivative followed by hydrogenation and if necessary converting a base or acid of the &agr;-aminosubstituted carboxylic acid amide into one of its salts.
    本发明涉及一种制备α-氨基取代的羧酸酰胺化合物及其盐的方法,包括将一级胺的羧酸酰胺与硝基化剂在碱存在下反应,随后通过水解得到羟基亚胺衍生物,然后进行氢化,并在必要时将α-氨基取代的羧酸酰胺的碱或酸转化为其盐之一。
  • [EN] FUSED PYRIMIDINE-DIONE DERIVATIVES AS TRPA1 MODULATORS<br/>[FR] DÉRIVÉS DE PYRIMIDINEDIONES FUSIONNÉS UTILISÉS COMME MODULATEURS DES RÉCEPTEURS TRPA1
    申请人:GLENMARK PHARMACEUTICALS SA
    公开号:WO2010109287A1
    公开(公告)日:2010-09-30
    The invention described herein relates to novel fused pyrimidinediones derivatives of formula (I) which are TRPA (Transient Receptor Potential subfamily A) modulators. In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders modulated by TRPAl (Transient Receptor Potential subfamily A, member 1). This invention also provides processes for preparing compounds described herein, intermediates used in their synthesis, pharmaceutical compositions thereof, and methods for treating or preventing diseases, conditions and/or disorders modulated by TRPAl. Formula (I)
    本发明描述的是一类新颖的杂合吡啶二酮衍生物,其化学公式为(I),这些衍生物是TRPA(瞬时受体电位亚家族A)的调节剂。特别是,本文所述的化合物对于治疗或预防由TRPA1(瞬时受体电位亚家族A成员1)调控的疾病、状况和/或失调是有用的。本发明还提供了制备所述化合物、它们合成中使用的中间体、药物组合物以及治疗或预防由TRPA1调控的疾病、状况和/或失调的方法。公式(I)
  • [EN] PYRIDAZINONE DERIVATIVES AND USE THEREOF AS P2X7 RECEPTOR INHIBITORS<br/>[FR] DÉRIVÉS DE PYRIDAZINONE ET LEUR UTILISATION COMME INHIBITEURS DU RÉCEPTEUR P2X7
    申请人:NISSAN CHEMICAL IND LTD
    公开号:WO2009057827A1
    公开(公告)日:2009-05-07
    Novel pyridazinone compounds of formula (I), which inhibit the purinergic P2X7 receptor and are useful for prevention, therapy and improvement of inflammatory and immunological diseases.
    翻译结果为:新型的哒嗪酮化合物,其化学公式为(I),能够抑制嘌呤能P2X7受体,并对预防、治疗和改善炎症性和免疫性疾病有益。
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