会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明授权
    • Aromatic imidocarbonate composition and method of use for combatting fungi
    • 芳香酰亚胺碳酸酯组合物和用于对抗真菌的方法
    • US3899582A
    • 1975-08-12
    • US43842574
    • 1974-01-31
    • SUMITOMO CHEMICAL CO
    • TANAKA SHIZUYAOZAKI TOSHIAKIMINE AKIHIKOTANAKA KATSUTOSHIYAMAMOTO SIGEOOOISHI TADASHIHINO NAGANORISATOMI TAKEO
    • C07D213/74A01N9/22
    • C07D213/74
    • Novel imidocarbonate derivatives having the formula:

      wherein Y and Z, which may be the same or different, are individually an oxygen or sulfur atom; Ar is an unsubstituted or a halogen- or lower C1 - C4 alkyl (straight or branched)substituted benzene or pyridine nucleus, the number of the substituents being 1 to 3; R2 is a C1 - C18 alkyl (straight or branched), a C1 - C18 alkyl(straight or branched) having 1 to 3 hydroxy radicals or 1 to 3 alkoxycarbonyl (the alkoxy has 1 to 4 carbon atoms) radicals in the carbon chain, a C3 - C10 cycloalkyl, a C2 - C5 alkenyl (straight or branched), a C3 - C6 alkynyl (straight or branched), a phenylalkyl, the benzene nucleus of which may be unsubstituted or substituted by 1 to 4 halogen atoms, 1 to 4 lower C1 - C4 alkyl (straight or branched) radicals or a nitro radical, or a halogen- or lower C1 - C4 alkyl (straight or branched)-substituted phenoxyalkyl; R3 is a C1 - C18 alkyl (straight or branched) having 1 to 3 hydroxy radicals or 1 to 3 alkoxycarbonyl (the alkoxy has 1 to 4 carbon atoms) radicals in the carbon chain, a C2 - C5 alkenyl (straight or branched), a C3 - C6 alkynyl (straight or branched) or a phenylalkyl, the benzene nucleus of which may be unsubstituted or substituted by 1 to 4 halogen atoms, 1 to 4 lower C1 - C4 alkyl (straight or branched) radicals, a nitro radical or a C2 - C4 alkylene radical, provided that in case Ar is an unsubstituted or substituted benzene nucleus and R2 and R3 are phenylalkyl groups, the benzene nucleus of at least one of said phenylalkyl groups has a substituent, have strong microbicidal activities on a wide scope of microorganisms.
    • 具有下式的新型亚氨基碳酸酯衍生物:Y-R2 Ar-N = C ANGLE Z-R3其中Y和Z可以相同或不同,分别为氧或硫原子; Ar是未取代的或卤素 - 或低级C 1 -C 4烷基(直链或支链)取代的苯或吡啶核,取代基数为1至3; R2是碳链中具有1至3个羟基或1至3个烷氧基羰基(烷氧基具有1至4个碳原子)的C1-C18烷基(直链或支链),C1-C18烷基(直链或支链) C3-C10环烷基,C2-C5烯基(直链或支链),C3-C6炔基(直链或支链),苯基烷基,其苯核可以是未取代的或被1-4个卤素原子取代,1〜 4个低级C1-C4烷基(直链或支链)基或硝基,或卤素 - 或低级C1-C4烷基(直链或支链)取代的苯氧基烷基; R3是碳链中具有1至3个羟基或1至3个烷氧基羰基(烷氧基具有1至4个碳原子)基团的C1-C18烷基(直链或支链),C2-C5链烯基(直链或支链) C 3 -C 6炔基(直链或支链)或苯基烷基,其苯核可以是未取代的或被1至4个卤素原子取代,1至4个低级C 1 -C 4烷基(直链或支链)基团,硝基或 如果Ar是未取代或取代的苯核,且R 2和R 3为苯基烷基,则所述苯基烷基中的至少一个的苯核具有取代基,在宽范围内具有强的杀微生物活性 的微生物。
    • 9. 发明专利
    • ISOTHIOUREA COMPOUNDS AND THEIR PRODUCTION AND USE
    • CA967960A
    • 1975-05-20
    • CA140
    • SUMITOMO CHEMICAL CO
    • TANAKA SHIZUYAYAMAMOTO SIGEOTANAKA KATSUTOSHITAKEDA HISAMI
    • C07D213/74
    • 1346958 1-Pyridyl-2-benzyl-isothioureas SUMITOMO CHEMICAL CO Ltd 12 April 1972 [30 April 1971] 16934/72 Heading C2C [Also in Division A5] Novel compounds of Formula (I) wherein M is a group of the formula -NR 1 R 2 in which R 1 is a hydrogen atom, a C 1-20 alkyl, cyano (C 1-5 )alkyl, C 1-5 alkenyl, C 1-5 alkynyl, or phenyl (C 1-5 ) alkyl group wherein the benzene ring is optionally substituted by one or more identical or different C 1-5 alkyl groups, one or more nitro groups and/or one or more identical or different halogen atoms, and in which R 2 is a C 1-20 alkyl, cyano (C 1-5 ) alkyl, C 1-5 alkenyl, C 1-5 alkynyl or phenyl (C 1-5 ) alkyl group wherein the benzene ring is optionally substituted by one or more identical or different C 1-5 alkyl groups, one or more nitro groups and/or one or more identical or different halogen atoms; or wherein M is a 3-6 membered heterocyclic group containing nitrogen as a heteroatom and optionally one or more further heteroatoms, the aforesaid heterocyclic group being bonded to the remainder of the isothiourea molecule by the said nitrogen heteroatom thereof; wherein X is a hydrogen atom, a halogen atom or a C 1-5 alkyl group; and wherein Y 1 , Y 2 and Y 3 are, each independently, a hydrogen atom, a nitro group, a halogen atom or a C 1-5 alkyl group, are prepared by reacting a thiourea of Formula (III) with a benzyl halide of Formula (IV) wherein Z is a halogen atom The preparation is preferably carried out in an inert solvent (e.g. MeOH, EtOH, THF, dioxane, DMSO or DMF) in the presence of a basic substance (e.g. NaOH, KOH, NaOMe, KOMe, NaOEt, Ca(OH) 2 ) generally using a molar ratio of base to benzyl halide to thiourea of 1-1À5: 1-2 : 1 respectively. The examples describe the preparation of many 1-(3 1 -pyridyl)-isothioureas which are effective against phyto-pathogenic bacteria or fungi or acarids.