摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

6-(butylthio)hexan-1-ol | 70190-28-2

中文名称
——
中文别名
——
英文名称
6-(butylthio)hexan-1-ol
英文别名
6-Butylsulfanylhexan-1-ol
6-(butylthio)hexan-1-ol化学式
CAS
70190-28-2
化学式
C10H22OS
mdl
——
分子量
190.35
InChiKey
GCYZTSYWWVDKAC-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):
    2.9
  • 重原子数:
    12
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    45.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    6-(butylthio)hexan-1-ol三甲基氯硅烷 、 sodium hydride 、 sodium iodide 作用下, 以 乙腈 为溶剂, 反应 14.0h, 生成 1-n-butylthiepanium iodide
    参考文献:
    名称:
    通过Me 3 SiI促进硫化物分子内置换氢氧化物或甲醇,形成环sulf盐。环收缩硫烷→硫烷
    摘要:
    适当定位的(1、2、1、1、4和1、5-)分子内硫化物会干扰碘代三甲基硅烷促进的碘的羟基取代,以及相关的醇脱保护步骤(甲基醚的区域选择性裂解)。结果可能是由于intermediate中间体的裂解而产生的环状an盐或碘化物。特别优选仲和叔醇或醚以及脂族而不是芳族硫化物官能团的环化。该反应的跨环形形式导致7元至5元环状硫化物的容易的环收缩。
    DOI:
    10.1016/0040-4020(96)00229-3
  • 作为产物:
    描述:
    丁硫醇1-己烯醇三(五氟苯基)硼烷 作用下, 反应 1.5h, 以87%的产率得到6-(butylthio)hexan-1-ol
    参考文献:
    名称:
    一种无过渡金属催化的不饱和烯烃制备硫醚的方法
    摘要:
    本发明涉及一种无过渡金属催化不饱和烯烃与硫酚反应制备硫醚的合成方法。该方法如下:在向反应管中加入不饱和烯烃底物和硫酚底物,然后加入催化量的三五氟苯基硼,在30‑80℃时反应1‑24小时后得到硫醚化合物。本发明的主要创新点在于不使用过渡金属催化剂即可高效制备硫醚化合物,避免了重金属污染。该方法具有绿色无溶剂、操作简便、条件温和、反应迅速、底物普适性好、和反应收率及选择性高等优点。
    公开号:
    CN111087331B
点击查看最新优质反应信息

文献信息

  • Scandium(III) Triflate-Catalyzed<i>anti</i>-Markovnikov Hydrothiolation of Functionalized Olefins
    作者:Krzysztof Kuciński、Piotr Pawluć、Grzegorz Hreczycho
    DOI:10.1002/adsc.201500720
    日期:2015.12.14
    Scandium(III) triflate promoted highly selective addition of thiols to functionalized olefins under mild conditions. The addition follows anti-Markovnikov regioselectivities, which are unusual for Lewis acids-catalyzed hydrothiolation. This reaction marks broad functional groups tolerance, which opens a beneficial synthetic route to functionalized and biologically active thio-compounds. This method
    在温和的条件下,三氟甲磺酸III(III)促进了硫醇向官能化烯烃的高度选择性加成。加入后具有抗-Markovnikov区域选择性,这对于路易斯酸催化的氢硫醇化作用是不寻常的。该反应标志着宽泛的官能团耐受性,这为功能化且具有生物活性的硫代化合物开辟了一条有益的合成途径。该方法广泛适用,并且以绿色方式提供了简单的后处理。
  • Pyrimidine nucleoside derivatives having anti-tumor activity, their preparation and use
    申请人:Sankyo Company Limited
    公开号:EP0536936A1
    公开(公告)日:1993-04-14
    Compounds of formula (I): [in which: R¹, R² and R³ are the same or different and each represents a hydrogen atom, an optionally substituted alkanoyl group or an alkenylcarbonyl group, provided that at least one of R¹, R² and R³ represents an unsubstituted alkanoyl group having from 5 to 24 carbon atoms, said substituted alkanoyl group or said alkenylcarbonyl group; and one of R⁴ and R⁵ represents a hydrogen atom and the other represents a cyano group]; have valuable anti-tumour activity.
    式子(I)的化合物:[其中:R¹、R²和R³相同或不同,每个代表氢原子、可选取代的脂肪酰基团或烯基羰基团,前提是至少有一个R¹、R²和R³代表有5到24个碳原子的未取代脂肪酰基团,或者是所述取代的脂肪酰基团或所述烯基羰基团;R⁴和R⁵中的一个代表氢原子,另一个代表氰基],具有有价值的抗肿瘤活性。
  • [DE] 1-AMINO-3-BENZYLURACILE<br/>[EN] 1-AMINO-3-BENZYLURACILS<br/>[FR] 1-AMINO-3-BENZYLURACILES
    申请人:BASF AKTIENGESELLSCHAFT
    公开号:WO1997001543A1
    公开(公告)日:1997-01-16
    (DE) 1-Amino-3-benzyluracile (I) und deren Salze (R1 = Halogen; R2, R3 = H, CN, SCN, Halogen, C1-C4-Halogenalkyl, C1-C4-Halogenalkoxy, C1-C4-Halogenalkylthio; R4 = R3 + C1-C4-Alkyl, C1-C4-Alkoxy, C1-C6-Alkyl-NH-CO-; R5 = H, CN, NO2, OH, Halogen, gegebenenfalls substituiertes NH2, gegebenenfalls subst. C1-C6-Halogenalkoxy, C1-C6-Halogenalkylthio, C1-C6-Alkoxy, C1-C6-Alkylthio, C3-C8-Cycloalkoxy, C3-C8-Cycloalkylthio, C3-C6-Alkenyloxy, C3-C6-Alkenylthio, C3-C6-Alkinyloxy, C3-C6-Alkinylthio, C1-C6-Alkyl-COO-, C1-C6-Alkyl-COS-, C3-C6-Alkenyl-COO-, C3-C6-Alkenyl-COS-, C3-C6-Alkinyl-COO-, C3-C6-Alkinyl-COS-, C1-C6-Alkyl-SO2-O- oder C1-C6-Alkyl-SO2-; R6 = 1) H, OH, SH, Halogen, C1-C6-Halogenalkoxy, C1-C6-Halogenalkylthio, C1-C6-Alkylthio-(C1-C6-alkyl)carbonyl, C1-C6-Alkyliminooxy-CO-, 2) gegebenenfalls subst. C1-C6-Alkoxy, C1-C6-Alkylthio, C3-C8-Cycloalkoxy, C3-C8-Cycloalkylthio, C2-C6-Alkenyloxy, C2-C6-Alkenylthio, C2-C6-Alkinyloxy, C2-C6-Alkinylthio, C1-C6-Alkyl-COO-, C2-C6-Alkyl-COS-, C1-C6-Alkoxy-COO-, C2-C6-Alkenyl-COO-, C2-C6-Alkenyl-COS-, C2-C6-Alkinyl-COO-, C2-C6-Alkinyl-COS-, C1-C6-Alkyl-SO2-O-, C1-C6-Alkyl-SO2-, 3) -CY-R11 Y = -O-, -S-, gegebenenfalls subst. -NH-}, -C(R11)(Z1R12)(Z2R13) Z1, Z2 = -O-, -S-}, -C(R11)=C(R14)-CN, -C(R11)=C(R14)-CO-R15, -CH(R11)-CH(R14)-CO-R15, -C(R11)=C(R14)-CH2-CO-R15, -C(R11)=C(R14)-C(R16)=C(R17)-CO-R15, -C(R11)=C(R14)-CH2-CH(R18)-CO-R15, -CO-OR19, -CO-SR19, -CO-N(R19)-OR20, -C$m(0)C-CO-NH-OR20, -C$m(0)C-CO-N(R19)-OR20, -C$m(0)C-CS-NH-OR20, -C$m(0)C-CS-N(R19)-OR20, -C(R11)=C(R14)-CO-NH-OR20, -C(R11)=C(R14)-CO-N(R19)-OR20, -C(R11)=C(R14)-CS-NH-OR20, -C(R11)=C(R14)-CS-N(R19)-OR20, -C(R11)=C(R14)-C(R21)=N-OR20, -C(R21)=N-OR20, -C$m(0)C-C(R21)=N-OR20, -C(Z1R12)(Z2R13)-OR19, -C(Z1R12) (Z2R13)-SR19, -C(Z1R12) (Z2R13)-N(R23)R24, gegebenenfalls substituiertes Amino oder -CONH2, Azaheterocyclyl, -CO-Azaheterocyclyl, (N + O oder N + O + S) Heterocyclyl enthaltende Kette); als Herbizide, zur Dessikation/Defoliation von Pflanzen.(EN) The invention concerns 1-amino-3-benzyluracils of formula (I) and their salts. In said formula (I), R1 = halogen; R2, R3 = H, CN, SCN, halogen, C1¿-C¿4-alkyl halide, C1-C4-alkoxy halide, C1-C4-alkylthio halide; R4 = R3 + C1-C4-alkyl, C1-C4-alkoxy, C1-C6-alkyl-NH-CO-; R5 = H, CN, NO2, OH, halogen, optionally substituted NH2, optionally substituted C1-C6-alkoxy halide, C1-C6-alkylthio halide, C1-C6-alkoxy, C1-C6-alkylthio, C3-C8-cycloalkoxy, C3-C8-cycloalkylthio, C3-C6-alkenyloxy, C3-C6-alkenylthio, C3-C6-alkinyloxy, C3-C6-alkinylthio, C1-C6-alkyl-COO-, C1-C6-alkyl-COS-, C3-C6-alkenyl-COO-, C3-C6-alkenyl-COS-, C3-C6-alkinyl-COO-, C3-C6-alkinyl-COS-, C1-C6-alkyl-SO2-O- or C1-C6-alkyl-SO2-; R6 = 1) H, OH, SH, halogen, C1-C6-alkoxy halide, C1C6-alkylthio halide, C1-C6-alkylthio-(C1-C6-alkyl)carbonyl, C1-C6-alkyliminooxy-CO-, 2) optionally substituted C1C6-alkoxy, C1-C6-alkylthio, C3-C8-cycloalkoxy, C3-C8-cycloalkylthio, C2-C6-alkenyloxy, C2-C6-alkenylthio, C2-C6-alkinyloxy, C2-C6-alkinylthio, C1-C6-alkyl-COO-, C2-C6-alkyl-COS-, C1-C6-alkoxy-COO-, C2-C6-alkenyl-COO-, C2-C6-alkenyl-COS-, C2-C6-alkinyl-COO-, C2-C6-alkinyl-COS-, C1-C6-alkyl-SO2-O-, C1-C6-alkyl-SO2-, 3) -CY-R11 Y = -O-, -S-, optionally substituted -NH-}, -C(R11)(Z1R12)(Z2R13) Z1, Z2 = -O-, -S-}, -C(R11)=C(R14)-CN, -C(R11)=C(R14)-CO-R15, -CH(R11)-CH(R14)-CO-R15, -C(R11)=C(R14)-CH2-CO-R15, -C(R11)=C(R14)-C(R16)=C(R17)-CO-R15, -C(R11)=C(R14)-CH2-CH(R18)-CO-R15, -CO-OR19, -CO-SR19, -CO-N(R19)-OR20, -C$m(0)C-CO-NH-OR20, -C$m(0)C-CO-N(R19)-OR20, -C$m(0)C-CS-NH-OR20, -C$m(0)C-CS-N(R19)-OR20, -C(R11)=C(R14)-CO-NH-OR20, -C(R11)=C(R14)-CO-N(R19)-OR20,-C(R11)=C(R14)-CS-NH-OR20, -C(R11)=C(R14)-CS-N(R19)-OR20, -C(R11)=C(R14)-C(R21)=N-OR20, -C(R21)=N-OR20, -C$m(0)C-C(R21)=N-OR20, -C(Z1R12)(Z2R13)-OR19, -C(Z1R12)(Z2R13)-SR19, -C(Z1R12)(Z2R13)-N(R23)R24, optionally substituted amino or -CONH2, azaheterocyclyl, -CO-azaheterocyclyl, or a chain comprising (N + O or N + O + S) heterocyclyl. These compounds can be used as herbicides for desiccating/defoliating plants.(FR) L'invention concerne des 1-amino-3-benzyluraciles de la formule (I) et leurs sels. Dans ladite formule (I), R1 représente de l'halogène; R2, R3 représentent H, CN, SCN, halogène, halogénure d'alkyle C1-C4, halogénure d'alcoxy C1-C4, halogénure d'alkylthio C1-C4; R4 représente R3 + alkyle C1-C4, alcoxy C1-C4, alkyle C1-C6 -NH-CO-; R5 représente H, CN, NO2, OH, halogène, NH2 éventuellement substitué, halogénure d'alcoxy C1-C6 éventuellement substitué, halogénure d'alkylthio C1-C6, alcoxy C1-C6, alkylthio C1-C6, cycloalcoxy C3-C8, cycloalkylthio C3-C8, alcényloxy C3-C6, alcénylthio C3-C6, alkinyloxy C3-C6, alkinylthio C3-C6, alkyle C1-C6-COO-, alkyle C1-C6-COS-, alcényle C3-C6-COO-, alcényle C3-C6-COS-, alkinyle C3-C6-COO-, alkinyle C3-C6-COS-, alkyle C1-C6-SO2-O- ou alkyle C1-C6-SO2-; R6 représente 1) H, OH, SH, halogène, halogénure d'alcoxy C1-C6, halogénure d'alkylthio C1-C6, alkylthio C1-C6-(alkyle C1-C6) carbonyle, alkyliminooxy C1-C6-CO-, 2) alcoxy C1-C6 éventuellement substitué, alkylthio C1-C6, cycloalcoxy C3-C8, cycloalkylthio C3-C8, alcényloxy C2-C6, alcénylthio C2-C6, alkinyloxy C2-C6, alkinylthio C2-C6, alkyle C1-C6-COO-, alkyle C2-C6-COS, alcoxy C1-C6-COO-, alcényle C2-C6-COO-, alcényle C2-C6 -COS-, alkinyle C2-C6-COO-, alkinyle C2-C6 -COS-, alkyle C1-C6-SO2-O-, alkyle C1-C6-SO2-, 3) -CY-R11 Y = -O-, -S-, -NH- éventuellement substitué}, -C(R11)(Z1R12)(Z2R13) Z1, Z2 = -O-, -S-}, -C(R11)=C(R14)-CN, -C(R11)=C(R14)-CO-R15, -CH(R11)-CH(R14)-CO-R15, -C(R11)=C(R14)-CH2-CO-R15, -C(R11)=C(R14)-C(R16)=C(R17)-CO-R15, -C(R11)=C(R14)-CH2-CH(R18)-CO-R15, -CO-OR19, -CO-SR19, -CO-N(R19)-OR20, -C$m(0)C-CO-NH-OR20, -C$m(0)C-CO-N(R19)-OR20, -C$m(0)C-CS-NH-OR20, -C$m(0)C-CS-N(R19)-OR20, -C(R11)=C(R14)-CO-NH-OR20, -C(R11)=C(R14)-CO-N(R19)-OR20, -C(R11)=C(R14)-CS-NH-OR20, -C(R11)=C(R14)-CS-N(R19)-OR20, -C(R11)=C(R14)-C(R21)=N-OR20, -C(R21)=N-OR20, -C$m(0)C-C(R21)=N-OR20, -C(Z1R12)(Z2R13)-OR19, -C(Z1R12)(Z2R13)-SR19, -C(Z1R12)(Z2R13)-N(R23)R24, amino éventuellement substitué ou -CONH2, azahétérocyclyle, -CO-azahétérocyclyle, ou une chaîne comprenant de un hétérocyclyle (N + O ou N + O + S). Ces composés chimiques peuvent être utilisés comme herbicides pour la dessication/défoliation des plantes.
    (DE)1-氨基-3-苯并嘧啶尿嘧啶(I)及其衍生物的盐类(R1 = 卤素;R2, R3 = H, CN, SCN, 卤素, C1-C4卤代烷基, C1-C4卤代烷氧基, C1-C4卤代烷硫基; R4 = R3 + C1-C4烷基, C1-C4烷氧基, C1-C6-NH-CO-烷基; R5 = H, CN, NO2, OH, 卤素, 可能是取代的NH2, 可能是取代的C1-C6卤代烷氧基, C1-C6卤代烷硫基, C1-C6烷氧基, C1-C6烷硫基, C3-C8环烷氧基, C3-C8环烷硫基, C3-C6烯基氧基, C3-C6烯基硫基, C3-C6炔基氧基, C3-C6炔基硫基, C1-C6烷基-COO-, C1-C6烷基-COS-, C3-C6烯基-COO-, C3-C6烯基-COS-, C3-C6炔基-COO-, C3-C6炔基-COS-, C1-C6烷基-SO2-O-或C1-C6烷基-SO2-; R6 = 1) H, OH, SH, 卤素, C1-C6卤代烷氧基, C1-C6卤代烷硫基, C1-C6烷硫基-(C1-C6烷基)羰基, C1-C6烷基亚胺氧基-CO-, 2) 可能是取代的C1-C6烷氧基, C1-C6烷硫基, C3-C8环烷氧基, C3-C8环烷硫基, C2-C6烯基氧基, C2-C6烯基硫基, C2-C6炔基氧基, C2-C6炔基硫基, C1-C6烷基-COO-, C2-C6烷基-COS-, C1-C6烷氧基-COO-, C2-C6烯基-COO-, C2-C6烯基-COS-, C2-C6炔基-COO-, C2-C6炔基-COS-, C1-C6烷基-SO2-O-, C1-C6烷基-SO2-, 3) -CY-R11 Y = -O-, -S-, 可能是取代的-NH-}, -C(R11)(Z1R12)(Z2R13) Z1, Z2 = -O-, -S-}, -C(R11)=C(R14)-CN, -C(R11)=C(R14)-CO-R15, -CH(R11)-CH(R14)-CO-R15, -C(R11)=C(R14)-CH2-CO-R15, -C(R11)=C(R14)-C(R16)=C(R17)-CO-R15, -C(R11)=C(R14)-CH2-CH(R18)-CO-R15, -CO-OR19, -CO-SR19, -CO-N(R19)-OR20, -C(*)(0)C-CO-NH-OR20, -C(*)(0)C-CO-N(R19)-OR20, -C(*)(0)C-CS-NH-OR20, -C(*)(0)C-CS-N(R19)-OR20, -C(R11)=C(R14)-CO-NH-OR20, -C(R11)=C(R14)-CO-N(R19)-OR20, -C(R11)=C(R14)-CS-NH-OR20, -C(R11)=C(R14)-CS-N(R19)-OR20, -C(R11)=C(R14)-C(R21)=N-OR20, -C(R21)=N-OR20, -C(*)(0)C-C(R21)=N-OR20, -C(Z1R12)(Z2R13)-OR19, -C(Z1R12)(Z2R13)-SR19, -C(Z1R12)(Z2R13)-N(R23)R24, 可能是取代的氨基或-CONH2, 含氮杂环基, -CO-含氮杂环基, 或包含(N + O或N + O + S)的杂环基链)。这些化合物可用作除草剂,用于植物的脱水/脱叶。 (EN)The invention concerns 1-amino-3-benzyluracils of formula (I) and their salts. In said formula (I), R1 = halogen; R2, R3 = H, CN, SCN, halogen, C1-C4-alkyl halide, C1-C4-alkoxy halide, C1-C4-alkylthio halide; R4 = R3 + C1-C4-alkyl, C1-C4-alkoxy, C1-C6-alkyl-NH-CO-; R5 = H, CN, NO2, OH, halogen, optionally substituted NH2, optionally substituted C1-C6-alkoxy halide, C1-C6-alkylthio halide, C1-C6-alkoxy, C1-C6-alkylthio, C3-C8-cycloalkoxy, C3-C8-cycloalkylthio, C3-C6-alkenyloxy, C3-C6-alkenylthio, C3-C6-alkinyloxy, C3-C6-alkinylthio, C1-C6-alkyl-COO-, C1-C6-alkyl-COS-, C3-C6-alkenyl-COO-, C3-C6-alkenyl-COS-, C3-C6-alkinyl-COO-, C3-C6-alkinyl-COS-, C1-C6-alkyl-SO2-O- or C1-C6-alkyl-SO2-; R6 = 1) H, OH, SH, halogen, C1-C6-alkoxy halide, C1-C6-alkylthio halide, C1-C6-alkylthio-(C1-C6-alkyl)carbonyl, C1-C6-alkyliminooxy-CO-, 2) optionally substituted C1-C6-alkoxy, C1-C6-alkylthio, C3-C8-cycloalkoxy, C3-C8-cycloalkylthio, C2-C6-alkenyloxy, C2-C6-alkenylthio, C2-C6-alkinyloxy, C2-C6-alkinylthio, C1-C6-alkyl-COO-, C2-C6-alkyl-COS-, C1-C6-alkoxy-COO-, C2-C6-alkenyl-COO-, C2-C6-alkenyl-COS-, C2-C6-alkinyl-COO-, C2-C6-alkinyl-COS-, C1-C6-alkyl-SO2-O-, C1-C6-alkyl-SO2-, 3) -CY-R11 Y = -O-, -S-, optionally substituted -NH-}, -C(R11)(Z1R12)(Z2R13) Z1, Z2 = -O-, -S-}, -C(R11)=C(R14)-CN, -C(R11)=C(R14)-CO-R15, -CH(R11)-CH(R14)-CO-R15, -C(R11)=C(R14)-CH2-CO-R15, -C(R11)=C(R14)-C(R16)=C(R17)-CO-R15, -C(R11)=C(R14)-CH2-CH(R18)-CO-R15, -CO-OR19, -CO-SR19, -CO-N(R19)-OR20, -C$(m)(0)C-CO-NH-OR20, -C$(m)(0)C-CO-N(R19)-OR20, -C$(m)(0)C-CS-NH-OR20, -C$(m)(0)C-CS-N(R19)-OR20, -C(R11)=C(R14)-CO-NH-OR20, -C(R11)=C(R14)-CO-N(R19)-OR20, -C(R11)=C(R14)-CS-NH-OR20, -C(R11)=C(R14)-CS-N(R19)-OR20, -C(R11)=C(R14)-C(R21)=N-OR20, -C(R21)=N-OR20, -C$(m)(0)C-C(R21)=N-OR20, -C(Z1R12)(Z2R13)-OR19, -C(Z1R12)(Z2R13)-SR19, -C(Z1R12)(Z2R13)-N(R23)R24, optionally substituted amino or -CONH2, azaheterocyclyl, -CO-azaheterocyclyl, or a chain comprising (N + O or N + O + S) heterocyclyl. These compounds can be used as herbicides for desiccating/defoliating plants. (FR)L'invention concerne des 1-amino-3-benzyluraciles de la formule (I) et leurs sels. Dans ladite formule (I), R1 représente de l'halogène; R2, R3 représentent H, CN, SCN, halogène, halogénure d'alkyle C1-C4, halogénure d'alcoxy C1-C4, halogénure d'alkylthio C1-C4; R4 représente R3 + alkyle C1-C4, alcoxy C1-C4, alkyle C1-C6 -NH-CO-; R5 Represents H, CN, NO2, OH, halogène, NH2 éventuellement substitué, halogénure d'alcoxy C1-C6 éventuellement substitué, halogénure d'alkylthio C1-C6, alcoxy C1-C6, alkylthio C1-C6, cycloalcoxy C3-C8, cycloalkylthio C3-C8, alcényloxy C3-C6, alcénylthio C3-C6, alkinyloxy C3-C6, alkinylthio C3-C6, alkyle C1-C6-COO-, alkyle C1-C6-COS-, alcényle C3-C6-COO-, alcényle C3-C6-COS-, alkinyle C3-C6-COO-, alkinyle C3-C6-COS-, alkyle C1-C6-SO2-O- ou alkyle C1-C6-SO2-; R6 représente 1) H, OH, SH, halogène, halogénure d'alcoxy C1-C6, halogénure d'alkylthio C1-C6, alkylthio C1-C6-(alkyle C1-C6) carbonyle, alkyliminooxy C1-C6-CO-, 2) alcoxy C1-C6 éventuellement substitué, alkylthio C1-C6, cycloalcoxy C3-C8, cycloalkylthio C3-C8, alcényloxy C2-C6, alcénylthio C2-C6, alkinyloxy C2-C6, alkinylthio C2-C6, alkyle C1-C6-COO-, alkyle C2-C6-COS, alcoxy C1-C6-COO-, alcényle C2-C6-COO-, alcényle C2-C6-COS-, alkinyle C2-C6-COO-, alkinyle C2-C6-COS-, alkyle C1-C6-SO2-O-, alkyle C1-C6-SO2-, 3) -CY-R11 Y = -O-, -S-, -NH- éventuellement substitué}, -C(R11)(Z1R12)(Z2R13) Z1, Z2 = -O-, -S-}, -C(R11)=C(R14)-CN, -C(R11)=C(R14)-CO-R15, -CH(R11)-CH(R14)-CO-R15, -C(R11)=C(R14)-CH2-CO-R15, -C(R11)=C(R14)-C(R16)=C(R17)-CO-R15, -C(R11)=C(R14)-CH2-CH(R18)-CO-R15, -CO-OR19, -CO-SR19, -CO-N(R19)-OR20, -C$(m)(0)C-CO-NH-OR20, -C$(m)(0)C-CO-N(R19)-OR20, -C$(m)(0)C-CS-NH-OR20, -C$(m)(0)C-CS-N(R19)-OR20, -C(R11)=C(R14)-CO-NH-OR20, -C(R11)=C(R14)-CO-N(R19)-OR20, -C(R11)=C(R14)-CS-NH-OR20, -C(R11)=C(R14)-CS-N(R19)-OR20, -C(R11)=C(R14)-C(R21)=N-OR20, -C(R21)=N-OR20, -C$(m)(0)C-C(R21)=N-OR20, -C(Z1R12)(Z2R13)-OR19, -C(Z1R12)(Z2R13)-SR19, -C(Z1R12)(Z2R13)-N(R23)R24, amino éventuellement substitué ou -CONH2, azahétérocyclyle, -CO-azahétérocyclyle, ou une chaîne comprenant de un hétérocyclyle (N + O ou N + O + S). Ces composés chimiques peuvent être utilisés comme herbicides pour la dessication/défoliation des plantes.
  • 1-AMINO-3-BENZYLURACILE
    申请人:BASF AKTIENGESELLSCHAFT
    公开号:EP0835248A1
    公开(公告)日:1998-04-15
  • VERFAHREN ZUR HERSTELLUNG VON ANELLIERTEN TRIAZOLEN UND NEUE ANELLIERTE TRIAZOLE UND DEREN VERWENDUNG
    申请人:BASF AKTIENGESELLSCHAFT
    公开号:EP1095045B1
    公开(公告)日:2003-01-15
查看更多