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1-(5-amino-2-chloro-4-fluorophenylthio)-cyclopropanecarboxylic acid ethyl ester | 140909-33-7

中文名称
——
中文别名
——
英文名称
1-(5-amino-2-chloro-4-fluorophenylthio)-cyclopropanecarboxylic acid ethyl ester
英文别名
ethyl 1-(5-amino-2-chloro-4-fluorophenyl)sulfanylcyclopropane-1-carboxylate
1-(5-amino-2-chloro-4-fluorophenylthio)-cyclopropanecarboxylic acid ethyl ester化学式
CAS
140909-33-7
化学式
C12H13ClFNO2S
mdl
——
分子量
289.758
InChiKey
DJLCQJFPWLSCPP-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):
    3.1
  • 重原子数:
    18
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    77.6
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    2-(5-amino-2-chloro-4-fluoro-phenylthio)-4-chlorobutyric acid ethyl ester 在 potassium carbonate 、 tetra(n-butyl)ammonium hydrogen sulfate 作用下, 以 甲苯 为溶剂, 生成 1-(5-amino-2-chloro-4-fluorophenylthio)-cyclopropanecarboxylic acid ethyl ester
    参考文献:
    名称:
    Herbicidally active thiadiazabicyclononanes and nonenes
    摘要:
    公式I的环烷基羧酸衍生物 其中W为##STR2##,A为CO--R.sub.3或CN;R.sub.1为氢或氟;R.sub.2为卤素或氰基;R.sub.3为氯、X--R.sub.5、氨基、C.sub.1-C.sub.4烷基氨基、d-C.sub.1-C.sub.4烷基氨基、C.sub.2-C.sub.4卤代烷基氨基、di-C.sub.2-C.sub.4卤代烷基氨基、C.sub.1-C.sub.4羟基烷基氨基、di-C.sub.1-C.sub.4羟基烷基氨基、C.sub.3-C.sub.4烯基氨基、二烯丙基氨基、--N-吡咯啉基、--N-哌啶基、--N-吗啉基、--N-硫代吗啉基、--N-哌嗪基、基团--O--N.dbd.C--(R.sub.9)R.sub.10或基团--N--R.sub.6(OR.sub.6);R.sub.4和R.sub.14分别独立地为氢、氟、氯、溴、C.sub.1-C.sub.4烷基或三氟甲基;R.sub.5为氢、C.sub.1-C.sub.10烷基、C.sub.1-C.sub.4烷氧基-C.sub.1-C.sub.4烷基、卤代-C.sub.1-C.sub.8烷基、C.sub.1-C.sub.10烷硫基-C.sub.1-C.sub.4烷基、二-C.sub.1-C.sub.4烷基氨基-C.sub.1-C.sub.4烷基、氰基-C.sub.1-C.sub.8烷基、C.sub.3-C.sub.8烯基、卤代-C.sub.3-C.sub.8烯基、C.sub.3-C.sub.8炔基、C.sub.3-C.sub.7环烷基、C.sub.3-C.sub.7环烷基-C.sub.1-C.sub.4烷基或卤代-C.sub.3-C.sub.7环烷基、或苄基,该苄基在苯环上未被取代或被选自卤素、C.sub.1-C.sub.4烷基、卤代-C.sub.1-C.sub.4烷基、卤代-C.sub.1-C.sub.4烷氧基或C.sub.1-C.sub.4烷氧基的最多三个相同或不同的取代基取代,或是碱金属离子、碱土金属离子或铵离子,该基团--[CHR.sub.6 --(CH.sub.2).sub.m ]--COOR.sub.7或基团[CHR.sub.6 --(CH.sub.2).sub.t --Si(R.sub.8).sub.3];R.sub.6为氢或C.sub.1-C.sub.4烷基;R.sub.7为氢、C.sub.1-C.sub.6烷基、C.sub.3-C.sub.8烯基、C.sub.3-C.sub.8炔基、C.sub.1-C.sub.8烷氧基-C.sub.2-C.sub.8烷基、C.sub.1-C.sub.8烷硫基-C.sub.2-C.sub.8烷基或C.sub.3-C.sub.7环烷基;R.sub.8为C.sub.1-C.sub.4烷基;R.sub.9为C.sub.1-C.sub.4烷基;R.sub.10为C.sub.1-C.sub.4烷基或苯基;或R.sub.9和R.sub.10与它们连接的碳原子一起形成一个环己烷环;R.sub.11为C.sub.1-C.sub.8烷基;R.sub.12为氢或C.sub.1-C.sub.8烷基;R.sub.13为氢、C.sub.1-C.sub.6烷基、C.sub.3-C.sub.7环烷基、C.sub.1-C.sub.4烷氧基-C.sub.1-C.sub.4烷基、C.sub.1-C.sub.4烷硫基-C.sub.1-C.sub.4烷基、卤代-C.sub.1-C.sub.7烷基、C.sub.3-C.sub.7烯基或C.sub.3-C.sub.7炔基;X、Y、Y.sub.1、Y.sub.2、Y.sub.3、Y.sub.4、Z.sub.1和Z.sub.2各自独立地为氧或硫;n为0、1、2、3或4;m为0、1、2、3或4;q为1或2;t为0、1、2、3或4。该衍生物具有良好的前后除草和生长调节性能。
    公开号:
    US05180418A1
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文献信息

  • US5180418A
    申请人:——
    公开号:US5180418A
    公开(公告)日:1993-01-19
  • Herbicidally active thiadiazabicyclononanes and nonenes
    申请人:Ciba-Geigy Corporation
    公开号:US05180418A1
    公开(公告)日:1993-01-19
    Cycloalkanecarboxylic acid derivatives of formula I ##STR1## wherein W is ##STR2## and A is CO--R.sub.3 or CN; R.sub.1 is hydrogen or fluorine; R.sub.2 is halogen or cyano; R.sub.3 is chlorine, X--R.sub.5, amino, C.sub.1 -C.sub.4 alkylamino, d-C.sub.1 -C.sub.4 alkylamino, C.sub.2 -C.sub.4 haloalkylamino, di-C.sub.2 -C.sub.4 haloalkylamino, C.sub.1 -C.sub.4 hydroxyalkylamino, di-C.sub.1 -C.sub.4 hydroxyalkylamino, C.sub.3 -C.sub.4 alkenylamino, diallylamino, --N-pyrrolidino, --N-piperidino, --N-morpholino, --N-thiomorpholino, --N-piperidazino, the group --O--N.dbd.C--(R.sub.9)R.sub.10 or the group --N--R.sub.6 (OR.sub.6); each of R.sub.4 and R.sub.14, independently of the other, is hydrogen, fluorine, chlorine, bromine, C.sub.1 -C.sub.4 alkyl or trifluoromethyl; R.sub.5 is hydrogen, C.sub.1 -C.sub.10 alkyl, C.sub.1 -C.sub.4 alkoxy-C.sub.1 -C.sub.4 alkyl, halo-C.sub.1 -C.sub.8 alkyl, C.sub.1 -C.sub.10 alkylthio-C.sub.1 -C.sub.4 alkyl, di-C.sub.1 -C.sub.4 alkylamino-C.sub.1 -C.sub.4 alkyl, cyano-C.sub.1 -C.sub.8 alkyl, C.sub.3 -C.sub.8 alkenyl, halo-C.sub.3 -C.sub. 8 alkenyl, C.sub.3 -C.sub.8 alkynyl, C.sub.3 -C.sub.7 cycloalkyl, C.sub.3 -C.sub.7 cycloalkyl-C.sub.1 -C.sub.4 alkyl or halo-C.sub.3 -C.sub.7 cycloalkyl, or benzyl which is unsubstituted or substituted at the phenyl ring by up to three identical or different substituents selected from halogen, C.sub.1 -C.sub.4 alkyl, halo-C.sub.1 -C.sub.4 alkyl, halo-C.sub.1 -C.sub.4 alkoxy or C.sub.1 -C.sub.4 alkoxy, or is an alkali metal ion, an alkaline earth metal ion or an ammonium ion, the group --[CHR.sub.6 --(CH.sub.2).sub.m ]--COOR.sub.7, or the group [CHR.sub.6 --(CH.sub.2).sub.t --Si(R.sub.8).sub.3 ]; R.sub.6 is hydrogen or C.sub.1 -C.sub.4 alkyl; R.sub.7 is hydrogen, C.sub.1 -C.sub.6 alkyl, C.sub.3 -C.sub.8 alkenyl, C.sub.3 -C.sub.8 alkynyl, C.sub.1 -C.sub.8 alkoxy-C.sub.2 -C.sub.8 alkyl, C.sub.1 -C.sub.8 alkylthio-C.sub.2 -C.sub.8 alkyl or C.sub.3 -C.sub.7 cycloalkyl; R.sub.8 is C.sub.1 - C.sub.4 alkyl; R.sub.9 is C.sub.1 -C.sub.4 alkyl; R.sub.10 is C.sub.1 -C.sub.4 alkyl or phenyl; or R.sub.9 and R.sub.10, together with the carbon atom to which they are bonded, form a cyclohexane ring; R.sub.11 is C.sub.1 -C.sub.8 alkyl; R.sub.12 is hydrogen or C.sub.1 -C.sub.8 alkyl; R.sub.13 is hydrogen, C.sub.1 -C.sub.6 alkyl, C.sub.3 -C.sub.7 cycloalkyl, C.sub.1 -C.sub.4 alkoxy-C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkylthio-C.sub.1 -C.sub.4 alkyl, halo-C.sub.1 -C.sub.7 alkyl, C.sub.3 -C.sub.7 alkenyl or C.sub.3 -C.sub.7 alkynyl; X, Y, Y.sub.1, Y.sub.2, Y.sub.3, Y.sub.4, Z.sub.1 and Z.sub.2 are each independently oxygen or sulfur; n is 0, 1, 2, 3 or 4; m is 0, 1, 2, 3 or 4; q is 1 or 2; and t is 0, 1, 2, 3 or 4, have good pre- and post-emergence selective herbicidal and growth regulating properties.
    公式I的环烷基羧酸衍生物 其中W为##STR2##,A为CO--R.sub.3或CN;R.sub.1为氢或氟;R.sub.2为卤素或氰基;R.sub.3为氯、X--R.sub.5、氨基、C.sub.1-C.sub.4烷基氨基、d-C.sub.1-C.sub.4烷基氨基、C.sub.2-C.sub.4卤代烷基氨基、di-C.sub.2-C.sub.4卤代烷基氨基、C.sub.1-C.sub.4羟基烷基氨基、di-C.sub.1-C.sub.4羟基烷基氨基、C.sub.3-C.sub.4烯基氨基、二烯丙基氨基、--N-吡咯啉基、--N-哌啶基、--N-吗啉基、--N-硫代吗啉基、--N-哌嗪基、基团--O--N.dbd.C--(R.sub.9)R.sub.10或基团--N--R.sub.6(OR.sub.6);R.sub.4和R.sub.14分别独立地为氢、氟、氯、溴、C.sub.1-C.sub.4烷基或三氟甲基;R.sub.5为氢、C.sub.1-C.sub.10烷基、C.sub.1-C.sub.4烷氧基-C.sub.1-C.sub.4烷基、卤代-C.sub.1-C.sub.8烷基、C.sub.1-C.sub.10烷硫基-C.sub.1-C.sub.4烷基、二-C.sub.1-C.sub.4烷基氨基-C.sub.1-C.sub.4烷基、氰基-C.sub.1-C.sub.8烷基、C.sub.3-C.sub.8烯基、卤代-C.sub.3-C.sub.8烯基、C.sub.3-C.sub.8炔基、C.sub.3-C.sub.7环烷基、C.sub.3-C.sub.7环烷基-C.sub.1-C.sub.4烷基或卤代-C.sub.3-C.sub.7环烷基、或苄基,该苄基在苯环上未被取代或被选自卤素、C.sub.1-C.sub.4烷基、卤代-C.sub.1-C.sub.4烷基、卤代-C.sub.1-C.sub.4烷氧基或C.sub.1-C.sub.4烷氧基的最多三个相同或不同的取代基取代,或是碱金属离子、碱土金属离子或铵离子,该基团--[CHR.sub.6 --(CH.sub.2).sub.m ]--COOR.sub.7或基团[CHR.sub.6 --(CH.sub.2).sub.t --Si(R.sub.8).sub.3];R.sub.6为氢或C.sub.1-C.sub.4烷基;R.sub.7为氢、C.sub.1-C.sub.6烷基、C.sub.3-C.sub.8烯基、C.sub.3-C.sub.8炔基、C.sub.1-C.sub.8烷氧基-C.sub.2-C.sub.8烷基、C.sub.1-C.sub.8烷硫基-C.sub.2-C.sub.8烷基或C.sub.3-C.sub.7环烷基;R.sub.8为C.sub.1-C.sub.4烷基;R.sub.9为C.sub.1-C.sub.4烷基;R.sub.10为C.sub.1-C.sub.4烷基或苯基;或R.sub.9和R.sub.10与它们连接的碳原子一起形成一个环己烷环;R.sub.11为C.sub.1-C.sub.8烷基;R.sub.12为氢或C.sub.1-C.sub.8烷基;R.sub.13为氢、C.sub.1-C.sub.6烷基、C.sub.3-C.sub.7环烷基、C.sub.1-C.sub.4烷氧基-C.sub.1-C.sub.4烷基、C.sub.1-C.sub.4烷硫基-C.sub.1-C.sub.4烷基、卤代-C.sub.1-C.sub.7烷基、C.sub.3-C.sub.7烯基或C.sub.3-C.sub.7炔基;X、Y、Y.sub.1、Y.sub.2、Y.sub.3、Y.sub.4、Z.sub.1和Z.sub.2各自独立地为氧或硫;n为0、1、2、3或4;m为0、1、2、3或4;q为1或2;t为0、1、2、3或4。该衍生物具有良好的前后除草和生长调节性能。
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