4-Chloro-3-[4-chloro-2-fluoro-5-carboxyphenyl]-5-difluoromethoxy-1-methyl-1H-pyrazole | 129631-53-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 4-Chloro-3-[4-chloro-2-fluoro-5-carboxyphenyl]-5-difluoromethoxy-1-methyl-1H-pyrazole
• 英文别名: 2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzoic acid；2-chloro-5-[4-chloro-5-(difluoromethoxy)-1-methylpyrazol-3-yl]-4-fluorobenzoic acid
• CAS: 129631-53-4
• 化学式: C₁₂H₇Cl₂F₃N₂O₃
• 分子量: 355.1
• InChiKey: FLMSFMQXCJQPKA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  22
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  64.4
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  N-甲基-N-(1-甲基乙基)氨基磺酰胺 、 4-Chloro-3-[4-chloro-2-fluoro-5-carboxyphenyl]-5-difluoromethoxy-1-methyl-1H-pyrazole 在 di-aza-bicycloundecene 、 N,N'-羰基二咪唑 作用下， 以 四氢呋喃 为溶剂， 以0.45 g (16.4%)的产率得到4-chloro-3-[4-chloro-2-fluoro-5-(N-methyl-N-isopropyl)-sulfamoylcarboxamidophenyl]-5-difluoromethoxy-1-methyl-1H-pyrazole
  参考文献：
  名称：

  Uracil substituted phenyl sulfamoyl carboxamides

  摘要：

  新型尿嘧啶取代苯基磺酰基羧酰胺I1及其盐，其中A＝氧或硫；X1＝H、卤素、C1-C4-烷基；X2＝H、CN、CS—NH2、卤素、C1-C4-烷基、C1-C4-卤代烷基；X3＝H、CN、C1-C6-烷基、C1-C6-烷氧基烷基、C3-C7-环烷基、C3-C6-烯基、C3-C6-炔基、可选择地取代的苄基；R1、R2＝H、卤素、可选择地取代的羟基、C1-C10-烷基、C2-C10-烯基、C3-C10-炔基、C3-C7-环烷基、苯基、苄基或C5-C7-环烯基，或R1＋R2与它们连接的原子共同形成3-至7-成员杂环环；Q从描述中定义的Q1到Q40中选择。用途：作为除草剂；用于植物的干燥/落叶。

  公开号：

  US20020045550A1
• 作为产物：
  描述：

  2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzaldehyde 在 sodium hydroxide 、 氢化钾 作用下， 以 水 为溶剂， 以56%的产率得到4-Chloro-3-[4-chloro-2-fluoro-5-carboxyphenyl]-5-difluoromethoxy-1-methyl-1H-pyrazole
  参考文献：
  名称：

  3-(substituted phenyl)pyrazole derivatives, salts thereof, and

  摘要：

  所揭示了一种由通式##STR1##表示的(3-取代苯基)吡唑衍生物，其中R.sup.1、R.sup.2、R.sup.3、R.sup.4和X为各种取代基及其盐，以及其生产过程。所述的吡唑衍生物或其盐可用作控制各种有害杂草的除草剂。

  公开号：

  US05032165A1

文献信息

• Substituted 1-methyl-3-phenylpyrazoles and the use thereof as herbicides
  申请人：BASF Aktiengesellschaft

  公开号：US05962694A1

  公开（公告）日：1999-10-05

  Substituted 1-methyl-3-phenylpyrazoles I and their agriculturally useful acid addition salts ##STR1## where R.sup.1 =C.sub.1 -C.sub.4 -haloalkoxy or C.sub.1-C.sub.4 -haloalkylthio; R.sup.2 =halogen; R.sup.3 =F or Cl; R.sup.4 =CN, C.sub.1 -C.sub.4 -fluoroalkyl, C.sub.2 -C.sub.4 -fluoroalkenyl or --C(R.sup.5)(X-R.sup.6)(Y-R.sup.7); R.sup.5 =H or C.sub.1 -C.sub.4 -alkyl; X and Y=--O-- or --S--; R.sup.6, R.sup.7 =C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.3 -C.sub.4 -alkenyl, C.sub.3 -C.sub.4 -haloalkenyl or C.sub.3 -C.sub.4 -alkynyl; are used as herbicides; for the desiccation/defoliation of plants.

  取代了1-甲基-3-苯基吡唑烯I及其在农业上有用的酸盐添加物##STR1##其中R.sup.1 =C.sub.1 -C.sub.4 -卤代烷氧基或C.sub.1-C.sub.4 -卤代硫基; R.sup.2 =卤素; R.sup.3 =F或Cl; R.sup.4 =CN, C.sub.1 -C.sub.4 -氟代烷基, C.sub.2 -C.sub.4 -氟代烯基或--C(R.sup.5)(X-R.sup.6)(Y-R.sup.7); R.sup.5 =H或C.sub.1 -C.sub.4 -烷基; X和Y=--O--或--S--; R.sup.6, R.sup.7 =C.sub.1 -C.sub.4 -烷基, C.sub.1 -C.sub.4 -卤代烷基, C.sub.3 -C.sub.4 -烯基, C.sub.3 -C.sub.4 -卤代烯基或C.sub.3 -C.sub.4 -炔基; 用作除草剂; 用于植物的干燥/落叶。
• Substituted 3-phenylpyrazoles
  申请人：BASF Aktiengesellschaft

  公开号：US06197973B1

  公开（公告）日：2001-03-06

  3-phenylpyrazoles of formula I wherein R1 is cyano, alkyl or haloalkyl; R2 is cyano or is optionally halogenated alkyl, alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; R3 is hydrogen, cyano, halogen, alkyl or haloalkyl; R4 is hydrogen or halogen; R5 is cyano, halogen, or is optionally halogenated alkyl or alkoxy; R6, R7 independently of one another are optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl or phenyl, optionally substituted alkylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl or optionally halogenated alkylsulfonyl; X is a chemical bond, —C≡C—, —CH2—CH(R8)— or —CH═C(R8)—, wherein R8 is hydrogen, cyano, nitro, halogen, alkyl or haloalkyl; Y is oxygen or sulfur; their preparation and their use for controlling undesirable vegetation.

  式I中的3-苯基吡唑，其中R1为氰基，烷基或卤代烷基；R2为氰基或可选卤代烷基，烷氧基，烷硫基，烷基亚磺酰基或烷基磺酰基；R3为氢，氰基，卤素，烷基或卤代烷基；R4为氢或卤素；R5为氰基，卤素，或可选卤代烷基或烷氧基；R6，R7分别独立地为可选取代的烷基，烯基，炔基，环烷基，杂环基或苯基，可选取代的烷基羰基，烷氧羰基，氨基羰基，烷基氨基羰基，双烷基氨基羰基或可选卤代烷基磺酰基；X为化学键，—C≡C—，—CH2—CH(R8)—或—CH═C(R8)—，其中R8为氢，氰基，硝基，卤素，烷基或卤代烷基；Y为氧或硫；其制备方法及其用于控制不良植被的用途。
• URACIL SUBSTITUTED PHENYL SULFAMOYL CARBOXAMIDES
  申请人：——

  公开号：US20040220172A1

  公开（公告）日：2004-11-04

  Novel uracil substituted phenyl sulfanoyl carboxamides I 1 and salts thereof, where A=oxygen or sulfur; X 1 =H, halogen, C 1 -C 4 -alkyl; X 2 =H, CN, CS—NH 2 , halogen, C 1 -C 4 -alkyl, C 1 -C 4 -haloalkyl; X 3 =H, CN, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxyalkyl, C 3 -C 7 -cycloalkyl, C 3 -C 6 -alkenyl, C 3 -C 6 -alkynyl, optionally substituted benzyl; R 1 , R 2 =H, halogen, optionally substituted hydroxy, C 1 -C 10 -alkyl, C 2 -C 10 -alkenyl, C 3 -C 10 -alkynyl, C 3 -C 7 -cycloalkyl, phenyl, benzyl or C 5 -C 7 -cycloalkenyl, or R 1 +R 2 together with the atom to which they are attached form a 3- to 7-membered heterocyclic ring; Q is selected from Q 1 to Q 40 as defined in the description. Use: As herbicides; for the desiccation/defoliation of plants.

  新型尿嘧啶取代苯基磺酰基羧酰胺I1及其盐，其中A = 氧或硫；X1 = H、卤素、C1-C4烷基；X2 = H、CN、CS—NH2、卤素、C1-C4烷基、C1-C4卤代烷基；X3 = H、CN、C1-C6烷基、C1-C6烷氧基烷基、C3-C7环烷基、C3-C6烯基、C3-C6炔基、可选取代苄基；R1、R2 = H、卤素、可选取代羟基、C1-C10烷基、C2-C10烯基、C3-C10炔基、C3-C7环烷基、苯基、苄基或C5-C7环烯基，或R1+R2结合成3-至7-成员杂环环；Q从Q1到Q40中选择，如描述中所定义。用途：作为除草剂；用于植物的脱水/落叶。
• [DE] SUBSTITUIERTE 3-PHENYLPYRAZOLE<br/>[EN] SUBSTITUTED 3-PHENYL PYRAZOLES<br/>[FR] 3-PHENYLPYRAZOLES SUBSTITUES
  申请人：BASF AKTIENGESELLSCHAFT

  公开号：WO1998005649A1

  公开（公告）日：1998-02-12

  (DE) Verbindungen der Formel (I) und deren Salze R1 = C1-C4-Alkyl, C1-C4-Halogenalkyl; R2 = CN, C1-C4-Alkyl, C1-C4-Halogenalkyl, C1-C4-Alkoxy, C1-C4-Halogenalkoxy, C1-C4-Alkylthio, C1-C4-Halogenalkylthio, C1-C4-Alkylsulphinyl, C1-C4-Halogenalkylsulphinyl, C1-C4-Alkylsulphonyl, C1-C4-Halogenalkylsulphonyl; R3 = H, CN, Halogen, C1-C4-Alkyl, C1-C4-Halogenalkyl; R4 = H, Halogen; R5 = CN, Halogen, C1-C4-Alkyl, C1-C4-Halogenalkyl, C1-C4-Alkoxy, C1-C4-Halogenalkoxy; R6, R7 = C1-C6-Alkyl, C1-C6-Halogenalkyl, Hydroxy-C1-C4-alkyl, Cyano-C1-C4-alkyl, C1-C4-Alkoxy-C1-C4-alkyl, C1-C4-Halogenalkoxy-C1-C4-alkyl, C3-C4-Alkenyloxy-C1-C4-alkyl, C3-C4-Alkinyloxy-C1-C4-alkyl, C3-C8-Cycloalkyloxy-C1-C4-alkyl, Amino-C1-C4-alkyl, C1-C4-Alkylamino-C1-C4-alkyl, Di(C1-C4-alkyl)amino-C1-C4-alkyl, C1-C4-Alkylthio-C1-C4-alkyl, C1-C4-Halogenalkylthio-C1-C4-alkyl, C3-C4-Alkenylthio-C1-C4-alkyl, C3-C4-Alkinylthio-C1-C4-alkyl, C1-C4-Alkylsulphinyl-C1-C4-alkyl, C1-C4-Halogenalkylsulphinyl-C1-C4-alkyl, C3-C4-Alkenylsulphinyl-C1-C4-alkyl, C3-C4-Alkinylsulphinyl-C1-C4-alkyl, C1-C4-Alkylsulphonyl-C1-C4-alkyl, C1-C4-Halogenalkylsulphonyl-C1-C4-alkyl, C3-C4-Alkenylsulphonyl-C1-C4-alkyl, C3-C4-Alkinylsulphonyl-C1-C4-alkyl, C3-C6-Alkenyl, Cyano-C3-C6-alkenyl, C3-C6-Halogenalkenyl, C3-C6-Alkinyl, Cyano-C3-C6-alkinyl, C3-C6-Halogenalkinyl, (C1-C4-Alkyl)carbonyl, (C1-C4-Halogenalkyl)carbonyl, (C1-C4-Alkoxy)carbonyl, H2N-CO, (C1-C4-Alkyl)NH-CO; (C1-C4-Alkyl)2N-CO, (C1-C4-Alkoxy-C1-C4-alkyl)carbonyl, C1-C4-Alkyl-SO2-, C1-C4-Halogenalkyl-SO2-, (C1-C4-Alkyl)carbonyl-C1-C4-alkyl, (C1-C4-Halogenalkyl)-carbonyl-C1-C4-alkyl, (C3-C8-Cycloalkyl)carbonyl-C1-C4-alkyl, (C1-C4-Alkoxy)imino-C1-C4-alkyl, (C3-C4-Alkenyloxy)imino-C1-C4-alkyl, Hydroxycarbonyl-C1-C4-alkyl, geg. subst. (C1-C4-Alkoxy)carbonyl-C1-C4-alkyl, (C1-C4-Halogenalkoxy)-carbonyl-C1-C4-alkyl, (C1-C4-Alkylthio)carbonyl-C1-C4-alkyl, H2NCO-C1-C4-alkyl, (C1-C4-Alkylamino)carbonyl-C1-C4-alkyl, Di(C1-C4-alkyl)aminocarbonyl-C1-C4-alkyl, gegebenenfalls substituiertes C3-C8-Cycloalkyl, C3-C8-Cycloalkyl-C1-C4-alkyl, Phenyl, Phenyl-C1-C4-alkyl, 3- bis 7-gliedriges Heterocyclyl or Heterocyclyl-C1-C4-alkyl, wobei alle Cycloalkyl- oder Heterocyclylringe CO oder CS enthalten können; X = Bindung, -C$m(Z)C-, *-CH2-CH(R8)- oder *-CH=C(R8)- (Stern = Bindung zum Phenylring; R8 = H, CN, NO2, Halogen, C1-C4-Alkyl, C1-C4-Halogenalkyl); Y = O, S} als Herbizide.(EN) Compounds having the formula (I) and their salts are useful as herbicides. In the formula R1 = C1-C4-alkyl, halogenated C1-C4-alkyl, R2 = CN, C1-C4-alkyl, halogenated C1-C4-alkyl, C1-C4-alkoxy, halogenated C1-C4-alkoxy, C1-C4-alkylthio, halogenated C1-C4-alkylthio, C1-C4-alkylsulphinyl, halogenated C1-C4-alkylsulphinyl, C1-C4-alkylsulphonyl, halogenated C1-C4-alkylsulphonyl; R3 = H, CN, halogen, C1-C4-alkyl, halogenated C1-C4-alkyl; R4 = H, halogen; R5 = CN, halogen, C1-C4-alkyl, halogenated C1-C4-alkyl, C1-C4-alkoxy, halogenated C1-C4-alkoxy; R6, R7 = C1-C6-alkyl, halogenated C1-C6-alkyl, hydroxy-C1-C4-alkyl, cyano-C1-C4-alkyl, C1-C4-alkoxy-C1-C4-alkyl, halogenated C1-C4-alkoxy-C1-C4-alkyl, C3-C4-alkenyloxy-C1-C4-alkyl, C3-C4-alkinyloxy-C1-C4-alkyl, C3-C8-cycloalkyloxy-C1-C4-alkyl, amino-C1-C4-alkyl, C1-C4-alkylamino-C1-C4-alkyl, di(C1-C4-alkyl)amino-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, halogenated C1-C4-alkylthio-C1-C4-alkyl, C3-C4-alkenylthio-C1-C4-alkyl, C3-C4-alkinylthio-C1-C4-alkyl, C1-C4-alkylsulphinil-C1-C4-alkyl, halogenated C1-C4-alkylsulphinyl-C1-C4-alkyl, C3-C4-alkenylsulphinyl-C1-C4-alkyl, C3-C4-alkinylsulphinyl-C1-C4-alkyl, C1-C4-alkylsulphonyl-C1-C4-alkyl, halogenated C1-C4-alkylsulphonyl-C1-C4-alkyl, C3-C4-alkenylsulphonyl-C1-C4-alkyl, C3-C4-alkinylsulphonyl-C1-C4-alkyl, C3-C6-alkenyl, cyano-C3-C6-alkenyl, halogenated C3-C6-alkenyl, C3-C6-alkinyl, cyano-C3-C6-alkinyl, halogenated cyano-C3-C6-alkinyl, (C1-C4-alkyl)carbonyl, (halogenated C1-C4-alkyl)carbonyl, (C1-C4-alkoxy)carbonyl, H2N-CO, (C1-C4-alkyl)NH-CO; (C1-C4-alkyl)2N-CO, (C1-C4-alkoxy- C1-C4-alkyl)carbonyl, C1-C4-alkyl-SO2-, halogenated C1-C4-alkyl-SO2-, (C1-C4-alkyl)carbonyl- C1-C4-alkyl, (halogenated C1-C4-alkyl)-carbonyl- C1-C4-alkyl, (C3-C8-cycloalkyl)carbonyl- C1-C4-alkyl, (C1-C4-alkoxy)imino- C1-C4-alkyl, (C3-C4-alkenyloxy)imino- C1-C4-alkyl, hydroxycarbonyl- C1-C4-alkyl, optionally substituted (C1-C4-alkoxy)carbonyl- C1-C4-alkyl, (halogenated C1-C4-alkoxy)-carbonyl- C1-C4-alkyl, (C1-C4-alkylthio)carbonyl- C1-C4-alkyl, H2NCO- C1-C4-alkyl, (C1-C4-alkylamino)carbonyl- C1-C4-alkyl, di(C1-C4-alkyl)aminocarbonyl- C1-C4-alkyl, optionally substituted C3-C8-cycloalkyl, C3-C8-cycloalkyl- C1-C4-alkyl, phenyl, phenyl- C1-C4-alkyl, 3- to 7-membered heterocyclyl or heterocyclyl- C1-C4-alkyl, whereas all cycloalkyl or heterocyclyl rings may contain CO or Cs; X stands for a bond, -C$m(Z)C-, *-CH2-CH(R8)- or *-CH=C(R8)- (asterisk = bond with the phenyl ring; R8 = H, CN, NO2, halogen, C1-C4-alkyl, halogenated C1-C4-alkyl); and Y = O, S}(FR) L'invention concerne des composés de la formule (I) et leurs sels utilisés comme herbicides; R1 = alkyle C1-C4, halogénure d'alkyle C1-C4; R2 = CN, alkyle C1-C4, halogénure d'alkyle C1-C4, alcoxy C1-C4, halogénure d'alcoxy C1-C4, alkylthio C1-C4, halogénure d'alkylthio C1-C4, akylsulfinyle C1-C4, halogénure d'alkylsulfinyle C1-C4, alkylsulfonyle C1-C4, halogénure akylsulfonyle C1-C4; R3 = H, CN, halogène, alkyle C1-C4, halogénure d'alkyle C1-C4; R4 = H, halogène; R5 = CN, halogène, alkyle C1-C4, halogénure d'alkyle C1-C4, alcoxy C1-C4, halogénure d'alcoxy C1-C4; R6, R7 = alkyle C1-C6, halogénure d'alkyle C1-C6, hydroxy-alkyle C1-C4, cyano-alkyle C1-C4, alcoxy C1-C4-alkyle C1-C4, halogénure d'alcoxy C1-C4-alkyle C1-C4, alkényloxy C3-C4-alkyle C1-C4, alkinyloxy C3-C4alkyle C1-C4, cycloalkyloxy C3-C8-alkyle C1-C4, amino-alkyle C1-C4, alkylamino C1-C4-alkyle C1-C4, di(alkyle C1-C4)amino-alkyle C1-C4, alkylthio C1-C4-alkyle C1-C4, halogénure d'alkylthio C1-C4-alkyle C1-C4, alkénylthio C3-C4-alkyle C1-C4, alkinylthio C3-C4-alkyle C1-C4, alkylsulfinyle C1-C4-alkyle C1-C4, halogénure d'alkylsulfinyle C1-C4-alkyle C1-C4-alkyle C1-C4, alkénylsulfinyle C3-C4-alkyle C1-C4, alkinylsulfinyle C3-C4-alkyle C1-C4, alkylsulfonyle C1-C4-alkyle C1-C4, halogénure d'alkylsulfonyle C1-C4-alkyle C1-C4, alkénylsulfonyle C3-C4-alkyle C1-C4, alkinylsulfonyle C3-C4-alkyle C1-C4, alkényle C3-C6, cyano-alkényle C3-C6, halogénure d'alkényle C3-C6, alkinyle C3-C6, cyano-alkinyle C3-C6, halogénure d'alkinyle C3-C6, (alkyle C1-C4)carbonyle, (halogénure d'alkyle C1-C4)carbonyle, (alcoxy C1-C4)carbonyle, H2N-CO, (alkyle C1-C4)NH-CO; (alkyle C1-C4)2N-CO, (alcoxy C1-C4-alkyle C1-C4)carbonyle, alkyle C1-C4-SO2, halogénure d'alkyle C1-C4-SO2-(alkyle C1-C4)carbonyle-alkyle C1-C4, (halogénure d'alkyle C1-C4)carbonyle-alkyle C1-C4, (cycloalkyle C3-C8)carbonyle-alkyle C1-C4, (alcoxy C1-C4)imino-alkyle C1-C4, (alkényloxy C3-C4)imino-alkyle C1-C4, hydroxycarbonyle-alkyle C1-C4, (alcoxy C1-C4)carbonyle-alkyle C1-C4 éventu. subst., (halogénure d'alcoxy C1-C4)carbonyle-alkyle C1-C4, (alkylthio C1-C4)carbonyle-alkyle C1-C4, H2NCO-alkyle C1-C4, (alkylamino C1-C4)carbonyle-alkyle C1-C4. di(alkyle C1-C4)aminocarbonyle-alkyle C1-C4, cycloalkyle C3-C8 éventuellement substitué, cycloalkyle C3-C8-alkyle C1-C4), phényle, phényle-alkyle C1-C4, hétérocyclyle ayant de 3 à 7 chaînons ou hétérocyclyle-alkyle C1-C4, tous les composés cycloalkyle ou hétérocyclyle pouvant contenir CO ou CS; X désigne une liaison, -C$m(Z)C-, *-CH2-CH(R8)- ou *-CH=C(R8)-(astérisque = liaison au composé cyclique phényle); R8 = H, CN, NO2, halogène, alkyle C1-C4, halogénure d'alkyle C1-C4); Y = O, S}.

  以下是将上述英文文本翻译成中文的版本： ( DE ) Verbindungen der Formel (I) und deren Salze R1 = C1-C4-alkyl, C1-C4-halogenalkyl; R2 = CN, C1-C4-alkyl, C1-C4-halogenalkyl, C1-C4-alkoxy, C1-C4-halogenalkoxy, C1-C4-alkylthio, C1-C4-halogenalkylthio, C1-C4-alkylsulphinyl, C1-C4-halogenalkylsulphinyl, C1-C4-alkylsulfonyl, C1-C4-halogenalkylsulfonyl; R3 = H, CN, halogen, C1-C4-alkyl, C1-C4-halogenalkyl; R4 = H, halogen; R5 = CN, halogen, C1-C4-alkyl, C1-C4-halogenalkyl, C1-C4-alkoxy, C1-C4-halogenalkoxy; R6, R7 = C1-C6-alkyl, C1-C6-halogenalkyl, hydroxy-C1-C4-alkyl, cyano-C1-C4-alkyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-halogenalkoxy-C1-C4-alkyl, C3-C4-alkenyloxy-C1-C4-alkyl, C3-C4-alkinyloxy-C1-C4-alkyl, C3-C8-cycloalkyloxy-C1-C4-alkyl, amino-C1-C4-alkyl, C1-C4-alkylamino-C1-C4-alkyl, di(C1-C4-alkyl)amino-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1-C4-halogenalkylthio-C1-C4-alkyl, C3-C4-alkenylthio-C1-C4-alkyl, C3-C4-alkinylthio-C1-C4-alkyl, C1-C4-alkylsulphinyl-C1-C4-alkyl, C1-C4-halogenalkylsulphinyl-C1-C4-alkyl, C3-C4-alkenylsulphinyl-C1-C4-alkyl, C3-C4-alkinylsulphinyl-C1-C4-alkyl, C1-C4-alkylsulfonyl-C1-C4-alkyl, C1-C4-halogenalkylsulfonyl-C1-C4-alkyl, C3-C4-alkenylsulfonyl-C1-C4-alkyl, C3-C4-alkinylsulfonyl-C1-C4-alkyl, C3-C6-alkenyl, cyano-C3-C6-alkenyl, C3-C6-halogenalkenyl, C3-C6-alkinyl, cyano-C3-C6-alkinyl, C3-C6-halogenalkinyl, (C1-C4-alkyl)carbonyl, (C1-C4-halogenalkyl)carbonyl, (C1-C4-alkoxy)carbonyl, H2NCO, (C1-C4-alkyl)NHCO; (C1-C4-alkyl)2NCO, (C1-C4-alkoxy-C1-C4-alkyl)carbonyl, C1-C4-alkyl-SO2, C1-C4-halogenalkyl-SO2, (C1-C4-alkyl)carbonyl-C1-C4-alkyl, (C1-C4-halogenalkyl)-carbonyl-C1-C4-alkyl, (C3-C8-cycloalkyl)carbonyl-C1-C4-alkyl, (C1-C4-alkoxy)imino-C1-C4-alkyl, (C3-C4-alkenyloxy)imino-C1-C4-alkyl, hydroxycarbonyl-C1-C4-alkyl, optionally substituted (C1-C4-alkoxy)carbonyl-C1-C4-alkyl, (C1-C4-halogenalkoxy)carbonyl-C1-C4-alkyl, (C1-C4-alkylthio)carbonyl-C1-C4-alkyl, H2NCO-C1-C4-alkyl, (C1-C4-alkylamino)carbonyl-C1-C4-alkyl, di(C1-C4-alkyl)aminocarbonyl-C1-C4-alkyl, optionally substituted C3-C8-cycloalkyl, C3-C8-cycloalkyl-C1-C4-alkyl, phenyl, phenyl-C1-C4-alkyl, 3-7-membered heterocyclyl or heterocyclyl-C1-C4-alkyl, whereas all cycloalkyl or heterocyclyl rings may contain CO or CS; X stands for a bond, -C$m(Z)C-, *-CH2-CH(R8)- or *-CH=C(R8)- (asterisk = bond to the phenyl ring; R8 = H, CN, NO2, halogen, C1-C4-alkyl, C1-C4-halogenalkyl); and Y = O, S}
• 3-(Substituted phenyl)pyrazole derivatives, salts thereof, herbicides therefrom, and process for producing said derivatives or salts
  申请人：NIHON NOHYAKU CO., LTD.

  公开号：EP0443059B1

  公开（公告）日：1998-06-17