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N-Trichloromethylthio-N-(2-Methoxy-5-pyridyl)-cyclopropane carboxamide

中文名称
——
中文别名
——
英文名称
N-Trichloromethylthio-N-(2-Methoxy-5-pyridyl)-cyclopropane carboxamide
英文别名
N-(6-methoxypyridin-3-yl)-N-(trichloromethylsulfanyl)cyclopropanecarboxamide
N-Trichloromethylthio-N-(2-Methoxy-5-pyridyl)-cyclopropane carboxamide化学式
CAS
——
化学式
C11H11Cl3N2O2S
mdl
——
分子量
341.646
InChiKey
UXDLANGIKBEFDT-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):
    3.4
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    67.7
  • 氢给体数:
    0
  • 氢受体数:
    4

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

  • 作为产物:
    参考文献:
    名称:
    Fungicidal N-(substituted thio)-pyridyl cyclopropane carboxamides
    摘要:
    具有一般结构式的新型杀真菌吡啶基环丙烷羧酰胺,其中R从卤代烷基、首选的C.sub.1-C.sub.3卤代烷基、C.sub.1-C.sub.8烷基、芳基、取代芳基和芳基烷基的组中选择,其中首选的芳基是苯基,烷基是C.sub.1-C.sub.3烷基,首选的取代基是Cl、Br、F和硝基、烷酰基,首选的C.sub.1-C.sub.4烷酰基,其中R.sub.3和R.sub.4可以是烷基、烷酰基、烷氧羰基、苄基吡啶基和取代吡啶基,R.sub.1是C.sub.1-C.sub.3烷氧基或C.sub.1-C.sub.3卤代烷氧基,首选是甲氧基或卤甲氧基和卤素,其中卤素是氯、溴或氟,R.sub.2是氢或甲基,以及其杀真菌活性良好的有机和无机盐,可用作预防和治疗真菌的高效杀真菌剂。这些化合物能够有效控制真菌生长。
    公开号:
    US04766135A1
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文献信息

  • Fungicidal pyridyl cyclopropane carboximides
    申请人:STAUFFER CHEMICAL COMPANY
    公开号:EP0243972A2
    公开(公告)日:1987-11-04
    Novel fungicidal pyridyl cyclopropane carboxamides having the general structural formula wherein Z is R is selected from the group consisting of cycloalkyl, preferably cyclopropyl, hydrogen, alkyl, haloalkyl, substituted alkyl, aryl, substituted aryl, heteroalkyl, alkenyl, OR1, SR, and wherein n is 0-10, preferably 0-2, ad R1 is C1-C4 alkyl; R2 is selected from the group consisting of halogen such as chlorine, fluorine and bromine, preferably chlorine, C1-C3 alkoxy such as propoxy ethoxy and methoxy, preferably methoxy and C1-C3 haloalkoxy; R3 is selected from the group consisting of hydrogen and methyl; X is oxygen or sulfur and Y is oxygen or sulfur; or Z is SR9 wherein R9 is selected from the group consisting of haloalkyl, preferably C1-C3 haloalkyl, C1-C8 alkyl, aryl, substituted aryl, and arylalkyl wherein the preferred aryl is phenyl, the alkyl is C1-C3 alkyl and the preferred substitutions are Cl, Br, F and nitro, alkanoyl, preferably C1-C4 alkanoyl, wherein R4 and R5 can be alkyl, alkanoyl, alkoxycarbonyl, benzyl, pyridyl and substituted pyridyl; provided that when Z is -SR9 Y is oxygen; and fungicidally acceptable organic and inorganic salts thereof which are highly effective fungicides for use both as preventive and curative fungicides are disclosed herein.
    具有通式结构的新型吡啶基环丙烷羧酰胺类杀菌剂 其中 Z 是 R选自由环烷基(最好是环丙基)、氢、烷基、卤代烷基、取代烷基、芳基、取代芳基、杂烷基、烯基、OR1、SR组成的组;以及 其中 n 为 0-10,优选 0-2,R1 为 C1-C4 烷基;R2 选自氯、氟和溴等卤素(优选氯)、丙氧基乙氧基和甲氧基等 C1-C3 烷氧基(优选甲氧基)以及 C1-C3 卤代烷氧基组成的组;R3 选自氢和甲基组成的组;X 是氧或硫,Y 是氧或硫;或 Z 是 SR9,其中 R9 选自由卤代烷基(优选 C1-C3 卤代烷基)、C1-C8 烷基、芳基、取代的芳基和芳烷基组成的组,其中优选的芳基是苯基,烷基是 C1-C3 烷基,优选的取代基是 Cl、Br、F 和硝基、烷酰基(优选 C1-C4 烷酰基)、 其中 R4 和 R5 可以是烷基、烷酰基、烷氧羰基、苄基、吡啶基和取代的吡啶基;但当 Z 为 -SR9 时,Y 为氧;本文公开了其杀真菌可接受的有机盐和无机盐,它们是高效的杀真菌剂,既可用作预防性杀真菌剂,也可用作治疗性杀真菌剂。
  • BAKER, DON R.;BROWNELL, KEITH H.
    作者:BAKER, DON R.、BROWNELL, KEITH H.
    DOI:——
    日期:——
  • US4766135A
    申请人:——
    公开号:US4766135A
    公开(公告)日:1988-08-23
  • US4977164A
    申请人:——
    公开号:US4977164A
    公开(公告)日:1990-12-11
  • Fungicidal N-(substituted thio)-pyridyl cyclopropane carboxamides
    申请人:ICI Americas Inc.
    公开号:US04977164A1
    公开(公告)日:1990-12-11
    Novel fungicidal pyridyl cyclopropane carboxamides having the general structural formula ##STR1## wherein R is selected from the group consisting of haloalkyl, preferably C.sub.1 -C.sub.3 haloalkyl, C.sub.1 -C.sub.8 alkyl, aryl, substituted aryl, and arylalkyl wherein the preferred aryl is phenyl, the alkyl is C.sub.1 -C.sub.3 alkyl and the preferred substitutions are Cl, Br, F and nitro, alkanoyl, preferably C.sub.1 -C.sub.4 alkanoyl, ##STR2## wherein R.sub.3 and R.sub.4 can be alkyl, alkanoyl, alkoxycarbanoyl, benzyl, pyridyl and substituted pyridyl, and when R.sub.3 and Rhd 4 are alkyl together with --N they can form a heterocyclic ring such as piperidine, R.sub.1 -C.sub.3 alkoxy or C.sub.1 -C.sub.3 haloalkoxy, preferably methoxy or halomethoxy and halogen wherein the halogen is chlorine, bromine or fluorine, R.sub.2 is hydrogen or methyl, and fungicidally acceptable organic and inorganic salts thereof which are highly effective fungicides for use both as preventive and curative fungicides are disclosed herein. These compounds provide excellent control of fungal growth.
    具有一般结构式##STR1##的新型杀真菌吡啶基环丙烷羧酰胺,其中R从卤代烷基,优选C.sub.1-C.sub.3卤代烷基,C.sub.1-C.sub.8烷基,芳基,取代芳基和芳基烷基中选择,其中优选芳基是苯基,烷基是C.sub.1-C.sub.3烷基,优选取代基是Cl,Br,F和硝基,烷酰基,优选C.sub.1-C.sub.4烷酰基,##STR2##其中R.sub.3和R.sub.4可以是烷基,烷酰基,烷氧羰基,苄基,吡啶基和取代吡啶基,当R.sub.3和R.sub.4与--N一起是烷基时,它们可以形成杂环环,如哌啶,R.sub.1-C.sub.3烷氧基或C.sub.1-C.sub.3卤代烷氧基,优选甲氧基或卤甲氧基和卤素,其中卤素是氯,溴或氟,R.sub.2是氢或甲基,以及其杀真菌有效的有机和无机盐,这些盐对预防和治疗真菌病害都非常有效,在此披露。这些化合物提供了对真菌生长的优异控制。
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