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    • 3. 发明授权
    • 3-hydrazono-benzisothiazole 1,1-dioxide fungicides
    • 3-肼基 - 苯并异噻唑1,1-二氧化物杀真菌剂
    • US4666930A
    • 1987-05-19
    • US707361
    • 1985-03-01
    • Herbert SalzburgManfred HajekGerd Hanssler
    • Herbert SalzburgManfred HajekGerd Hanssler
    • A01N43/80A01N47/24A01N47/34C07D275/06C07D417/12
    • C07D275/06A01N43/80A01N47/24A01N47/34C07D417/12
    • Compounds of the formula ##STR1## in which R.sup.1 is alkyl, cycloalkyl, aryl or hydrogen,R.sup.2 is --CO--R.sup.3,R.sup.3 is alkyl, alkenyl or cycloalkyl, or is phenyl which is optionally substituted, or is alkoxy or benzyl, or is phenoxy which is optionally substituted, or is phenoxymethyl, alkylamino, cycloalkylamino or phenylamino, orR.sup.1 and R.sup.2 together are a ##STR2## group, R.sup.4 and R.sup.5 each independently is hydrogen, alkyl, cycloalkenyl or phenylalkenyl, or is phenyl which is optionally substituted by alkyl, halogen and/or alkoxy, or is furyl, orR.sup.4 and R.sup.5 together are alkylene having 4 to 6 carbon atoms,are fungicidally active. Those compounds wherein R.sup.3 is alkylamino, cycloalkylamino or phenylamino, with the exception of the compound in which R.sup.1 is hydrogen and R.sup.6 is phenylamino, are new.
    • 式中,R 1为烷基,环烷基,芳基或氢的化合物,R 2为-CO-R 3,R 3为烷基,烯基或环烷基,或为任选取代的苯基,或为烷氧基或苄基,或为 任选被取代的苯氧基,或者是苯氧基甲基,烷基氨基,环烷基氨基或苯基氨基,或者R 1和R 2一起是一个基团,R 4和R 5各自独立地是氢,烷基,环烯基或苯基烯基,或者是任选地被 烷基,卤素和/或烷氧基,或是呋喃基,或R4和R5一起是具有4-6个碳原子的亚烷基,是杀真菌活性的。 其中R 3是烷基氨基,环烷基氨基或苯基氨基的那些化合物,除了其中R 1是氢和R 6是苯基氨基的化合物外,是新的。
    • 4. 发明授权
    • Salts of 2-keto-2H, 3H-1,2-benzisothiazole 1,1-dioxide as microbicides
    • US4683233A
    • 1987-07-28
    • US704439
    • 1985-02-22
    • Herbert SalzburgManfred HajekGerd HansslerVarl-Heinz Kuck
    • Herbert SalzburgManfred HajekGerd HansslerVarl-Heinz Kuck
    • A01N47/44A01N20060101A01N37/44A01N43/16A01N43/40A01N43/50A01N43/54A01N43/56A01N43/60A01N43/653A01N43/76A01N43/80A01N43/84A01N43/90A01N47/42
    • A01N43/56A01N37/44A01N43/16A01N43/40A01N43/50A01N43/54A01N43/60A01N43/653A01N43/76A01N43/80A01N43/84A01N43/90A01N47/44
    • A method of combating fungi and bacteria which comprises applying to such fungi, bacteria or a habitat thereof, a fungicidally or bactericidally effective amount of at least one salt of 3-keto-2-, 3H-1,2-benzisothiazole 1,1-dioxide of the formula ##STR1## in which R.sup.1 represents hydrogen, alkyl having 1 to 18 carbon atoms, or alkyl which has 1 to 6 carbon atoms and is optionally monosubstituted to trisubstituted by hydroxyl and/or monosubstituted to trisubstituted by amino, or represents carboxyl-substituted alkyl having 1 to 4 carbon atoms, or phenyl which is optionally monosubstituted to trisubstituted by identical or different substituents from amongst nitro and chlorine, or represents cycloalkyl having 5 or 6 carbon atoms, or represents heterocyclic structures which are optionally saturated or unsaturated, are optionally monosubstituted to tetrasubstituted by alkyl having 1 to 4 carbon atoms or hydroxyl, and have 1 to 3 identical or different heteroatoms, and a total of 5 or 6 ring members,R.sup.2 represents alkyl having 1 to 18 atoms, or alkyl which has 1 to 6 carbon atoms and is optionally monosubstituted to trisubstituted by hydroxyl and/or monosubstituted to trisubstituted by amino, or represents carboxyl-substituted alkyl having 1 to 4 carbon atoms, or phenyl which is optionally monosubstituted to trisubstituted by identical or different substituents from amongst nitro and chlorine, or represent cycloalkyl having 5 or 6 carbon atoms, or represents heterocyclic structures which are optionally saturated or unsaturated, are optionally monosubstituted to tetrasubstituted by alkyl having 1 to 4 carbon atoms or hydroxyl, and have 1 to 3 identical or different heteroatoms, and a total of 5 or 6 ring members, andR.sup.3 represents hydrogen, alkyl, having 1 to 6 carbon atoms, NH.sub.2, ##STR2## benzyl, or hydroxyalkyl having 1 to 3 carbon atoms, with the exception of the mono-, di- and triethanolamine compounds, orR.sup.1 and R.sup.2 together with the nitrogen atom at which they are located, form a 5-membered or 6-membered ring which can optionally contain further heteroatoms, and can optionally be substituted by keto groups or fused-on 5-membered or 6-membered rings and/or alkyl having 1 to 4 carbon atoms, with the exception of the pyridine ring which is optionally mono- or disubstituted by methyl.
    • 5. 发明授权
    • Process for the production of dianhydrohexitol mixtures and the
production of polymers from such mixtures
    • 用于制备二羟基己糖醇混合物的方法和由这些混合物生产聚合物
    • US4564645A
    • 1986-01-14
    • US689357
    • 1985-01-07
    • Herbert SalzburgManfred HajekHolger Meyborg
    • Herbert SalzburgManfred HajekHolger Meyborg
    • C07D493/04C08G18/32C08G18/30
    • C07D493/04C08G18/3218
    • Liquid dianhydrohexitol mixtures are prepared from diacylation products of hexitols and compounds such as organic carboxylic acids, carboxylic acid anhydrides, carboxylic acid halides, ketene and carbonic acid ester derivatives. More specifically, such diacylation products are simultaneously dehydrated and isomerized by subjecting them to a temperature of at least 130.degree. C. in the presence of a strong acid to yield diacylated dianhydro-hexitol isomer mixtures. These isomer mixtures are then converted to dianhydro-hexitol isomer mixtures by hydrolysis or transesterification. Suitable strong acids include proton acids, Lewis acids and heterogeneous acid catalysts (e.g., ion exchange resins). The mixtures of the present invention are characterized by a minimal tendency towards crystallization. These mixtures are particularly useful as chain extending agents in the production of polyurethanes.
    • 液体二脱水己糖醇混合物由己醇的二酰化产物和有机羧酸,羧酸酐,羧酸卤化物,乙烯酮和碳酸酯衍生物等化合物制备。 更具体地说,这样的二酰化产物通过在强酸存在下使其至少130℃的温度同时进行脱水和异构化,得到二酰化二脱氢 - 己糖醇异构体混合物。 然后通过水解或酯交换将这些异构体混合物转化为二脱氢己糖醇异构体混合物。 合适的强酸包括质子酸,路易斯酸和多相酸催化剂(如离子交换树脂)。 本发明的混合物的特征在于最小的结晶倾向。 这些混合物特别可用作聚氨酯生产中的扩链剂。
    • 6. 发明授权
    • Process for the production of dianhydrohexitol mixtures and liquid
mixture of dianhydrohexitols
    • 二脱水己醇混合物的生产方法和二脱水己醇的液体混合物
    • US4506086A
    • 1985-03-19
    • US515411
    • 1983-07-20
    • Herbert SalzburgManfred HajekHolger Meyborg
    • Herbert SalzburgManfred HajekHolger Meyborg
    • C07D493/04C08G18/32
    • C07D493/04C08G18/3218
    • Liquid dianhydrohexitol mixtures are prepared from diacylation products of hexitols and compounds such as organic carboxylic acids, carboxylic acid anhydrides, carboxylic acid halides, ketene and carbonic acid ester derivatives. More specifically, such diacylation products are simultaneously dehydrated and isomerized by subjecting them to a temperature of at least 130.degree. C. in the presence of a strong acid to yield diacylated dianhydrohexitol isomer mixtures. These isomer mixtures are then converted to dianhydrohexitol isomer mixtures by hydrolysis or transesterification. Suitable strong acids include proton acids, Lewis acids and heterogeneous acid catalysts (e.g., ion exchange resins). The mixtures of the present invention are characterized by a minimal tendency towards crystallization. These mixtures are particularly useful as chain extending agents in the production of polyurethanes.
    • 液体二脱水己糖醇混合物由己醇的二酰化产物和有机羧酸,羧酸酐,羧酸卤化物,乙烯酮和碳酸酯衍生物等化合物制备。 更具体地说,这样的二酰化产物通过在强酸存在下经受至少130℃的温度同时进行脱水和异构化,得到二酰基二脱水己糖异构体混合物。 然后通过水解或酯交换将这些异构体混合物转化成二羟基己糖异构体混合物。 合适的强酸包括质子酸,路易斯酸和多相酸催化剂(如离子交换树脂)。 本发明的混合物的特征在于最小的结晶倾向。 这些混合物特别可用作聚氨酯生产中的扩链剂。
    • 10. 发明授权
    • Process for the production of microcapsules
    • 微胶囊生产工艺
    • US4428983A
    • 1984-01-31
    • US310923
    • 1981-10-13
    • Ulrich NehenManfred HajekNorbert WeimannManfred Dahm
    • Ulrich NehenManfred HajekNorbert WeimannManfred Dahm
    • A61K9/50B01J13/14B01J13/16C09J5/00B01J13/02B05D7/00
    • B01J13/16Y10T428/2985Y10T428/2989
    • A process for encapsulating products in a polymer by interfacial polymerization, in which a stabilized dispersion of droplets of a first liquid which is to be encapsulated or a stabilized dispersion of solid particles which are to be encapsulated is formed in a continuous phase of a second liquid, and wherein one of the two capsule wall-forming reaction components is present in free form while the other of the two capsule wall-forming reaction components is present in reversibly blocked form, both reaction components are present in the first or second liquid without reacting with one another and the reaction component which is present in reversibly blocked form is deblocked by means of water present in the second or first liquid and then reacts with the reaction component present in free form to form a polymeric capsule wall, the droplets of the first liquid or the solid particles being encapsulated in small capsules consisting of polymeric material.
    • 通过界面聚合将产物包封在聚合物中的方法,其中待包封的第一液体的液滴的稳定分散体或待被包封的固体颗粒的稳定化分散体形成在第二液体的连续相中 ,并且其中两个胶囊壁形成反应组分中的一个以游离形式存在,而两个胶囊壁形成反应组分中的另一个以可逆阻挡的形式存在,两个反应组分都存在于第一或第二液体中而没有反应 彼此之间并且以可逆阻挡形式存在的反应组分通过存在于第二或第一液体中的水解封,然后与游离形式存在的反应组分反应形成聚合物胶囊壁,第一 液体或固体颗粒被包封在由聚合物材料组成的小胶囊中。