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2-(2,3,4,5,6-pentafluorobenzyl)malononitrile | 475197-86-5

中文名称
——
中文别名
——
英文名称
2-(2,3,4,5,6-pentafluorobenzyl)malononitrile
英文别名
(2,3,4,5,6-Pentafluorobenzyl)malononitrile;2-[(2,3,4,5,6-pentafluorophenyl)methyl]propanedinitrile
2-(2,3,4,5,6-pentafluorobenzyl)malononitrile化学式
CAS
475197-86-5
化学式
C10H3F5N2
mdl
——
分子量
246.139
InChiKey
AMDMWNFTQDILEK-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):
    2.4
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    47.6
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    2-(2,3,4,5,6-pentafluorobenzyl)malononitrile一水合肼 作用下, 以 甲醇 为溶剂, 反应 8.0h, 以33%的产率得到4-(2,3,4,5,6-pentafluorobenzyl)-1H-pyrazole-3,5-diamine
    参考文献:
    名称:
    The Synthesis of Some Derivatives Based on the 4-Benzyl-1H-pyrazole-3,5-diamine Core
    摘要:
    The three-step synthesis of 4-benzyl-1H-pyrazole-3,5-diamines 2 from commercially available aldehydes 3 is given. The Knoevenagel condensation was utilized to assemble the initial carbon framework, resulting in the benzylidenemalononitriles 4 which were directly transformed by the reduction of the electron deficient C=C bond to benzylmalononitriles 5. Subsequent cycloaddition of hydrazine with 5 afforded the desired pyrazoles 2. Due to the high similarity with 4-arylazo-1H-pyrazole-3,5-diamines, the biological activities of the 4-benzyl-1H-pyrazole-3,5-diamines 2 were evaluated while focusing on the inhibition of cyclin-dependent kinases (CDKs), but no significant results were obtained.
    DOI:
    10.3987/com-10-12101
  • 作为产物:
    描述:
    五氟苯甲醛哌啶 、 sodium cyanoborohydride 、 溶剂黄146 作用下, 以 四氢呋喃 为溶剂, 反应 27.0h, 生成 2-(2,3,4,5,6-pentafluorobenzyl)malononitrile
    参考文献:
    名称:
    The Synthesis of Some Derivatives Based on the 4-Benzyl-1H-pyrazole-3,5-diamine Core
    摘要:
    The three-step synthesis of 4-benzyl-1H-pyrazole-3,5-diamines 2 from commercially available aldehydes 3 is given. The Knoevenagel condensation was utilized to assemble the initial carbon framework, resulting in the benzylidenemalononitriles 4 which were directly transformed by the reduction of the electron deficient C=C bond to benzylmalononitriles 5. Subsequent cycloaddition of hydrazine with 5 afforded the desired pyrazoles 2. Due to the high similarity with 4-arylazo-1H-pyrazole-3,5-diamines, the biological activities of the 4-benzyl-1H-pyrazole-3,5-diamines 2 were evaluated while focusing on the inhibition of cyclin-dependent kinases (CDKs), but no significant results were obtained.
    DOI:
    10.3987/com-10-12101
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文献信息

  • Quinine catalysed asymmetric Michael additions in a sustainable solvent
    作者:José A. Castro-Osma、James W. Comerford、Samantha Heath、Oliver Jones、Maria Morcillo、Michael North
    DOI:10.1039/c4ra12132e
    日期:——

    Diethyl carbonate is shown to be a suitable, sustainable solvent in which to carry out quinine catalysed asymmetric Michael additions of malononitriles to enones.

    乙基碳酸酯被证明是一种适合的可持续溶剂,可用于进行奎宁催化的马来酸二腈对烯酮的不对称迈克尔加成反应。
  • Pesticide composition comprising malononitrile compounds
    申请人:——
    公开号:US20040142821A1
    公开(公告)日:2004-07-22
    The present invention relates to use of malononitrile compounds of formula (X): 1 wherein R 1 and R 2 are the same or different and independently C 1 -C 5 (halo)-alkyl, C 1 -C 5 (halo)alkyloxy, C 2 -C 5 (halo)alkenyl, C 2 -C 5 (halo)alkynyl, hydrogen, or cyano; R 3 and R 4 are the same or different and independently C 1 -C 10 alkyl, C 2 -C 10 alkenyl, C 2 -C 10 alkynyl, or hydrogen, or R 3 and R 4 are taken together to form C 2 -C 6 (halo)alkylene or C 4 -C 6 (halo)alkenylene; R 5 is halogen, cyano, nitro, C 1 -C 4 (halo)alkyl, or the like; n is an integer of 0 to 4; R 6 is halogen, cyano, nitro, C 1 -C 4 (halo)alkyl, or the like; or R 5 and R 6 are taken together to form methylenedioxy; with the provisos that when R 6 is hydrogen, then n is an integer of 1 to 4 and that when n is 2 or more, then R 5 's are different from each other; as pesticides, and to pesticide compositions containing these compounds as active ingredients. The present invention makes it possible to effectively control pests such as insect pests, acarine pests, and nematode pests.
    本发明涉及使用式(X)的丙二腈化合物:其中R1和R2相同或不同且独立地为C1-C5(卤)烷基,C1-C5(卤)烷氧基,C2-C5(卤)烯基,C2-C5(卤)炔基,氢或基;R3和R4相同或不同且独立地为C1-C10烷基,C2-C10烯基,C2-C10炔基或氢,或者R3和R4结合形成C2-C6(卤)烷基或C4-C6(卤)烯基;R5为卤素,基,硝基,C1-C4(卤)烷基或类似物;n为0至4的整数;R6为卤素,基,硝基,C1-C4(卤)烷基或类似物;或者R5和R6结合形成亚甲二氧基;但当R6为氢时,n为1至4的整数,且当n为2或更多时,R5不相同;作为杀虫剂,以及含有这些化合物作为活性成分的杀虫剂组合物。本发明使得能够有效地控制害虫,例如昆虫害虫,螨虫害虫和线虫害虫。
  • EP1385377A1
    申请人:——
    公开号:EP1385377A1
    公开(公告)日:2004-02-04
  • [EN] PESTICIDE COMPOSITION COMPRISING MALONONITRILE COMPOUNDS<br/>[FR] COMPOSITION PESTICIDE COMPRENANT DES COMPOSES DE MALONONITRILE
    申请人:SUMITOMO CHEMICAL CO
    公开号:WO2002089579A1
    公开(公告)日:2002-11-14
    The present invention relates to use of malononitrile compounds of formula (X): wherein R1 and R2 are the same or different and independently C1-C5 (halo)alkyl, C1-C5 (halo)alkyloxy, C2-C5 (halo)alkenyl, C2-C5 (halo)alkynyl, hydrogen, or cyano; R¿3? and R4 are the same or different and independently C?1-C10¿ alkyl, C2-C10 alkenyl, C2-C10 alkynyl, or hydrogen, or R¿3? and R4 are taken together to form C?2-C6¿ (halo)alkylene or C4-C6 (halo)alkenylene; R¿5? is halogen, cyano, nitro, C?1-C4¿ (halo)alkyl, or the like; n is an integer of 0 to 4; R¿6? is halogen, cyano, nitro, C?1-C4¿ (halo)alkyl, or the like; or R¿5? and R6 are taken together to form methylenedioxy; with the provisos that when R6 is hydrogen, then n is an integer of 1 to 4 and that when n is 2 or more, then R5's are different from each other; as pesticides, and to pesticide compositions containing these compounds as active ingredients. The present invention makes it possible to effectively control pests such as insect pests, acarine pests, and nematode pests.
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