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ZENTRALINSTITUT FUER ORGANISCH

Overview
  • Total Patents
    22
About

ZENTRALINSTITUT FUER ORGANISCH has a total of 22 patent applications. Its first patent ever was published in 1989. It filed its patents most often in Germany and German Democratic Republic. Its main competitors in its focus markets organic fine chemistry, basic materials chemistry and materials and metallurgy are CHENGDU CARDIFF TECH CO LTD, BTC PHARMACEUTICALS TECH CO LTD and CHANGZHOU WOTENG CHEMICAL TECH CO LTD.

Patent filings in countries

World map showing ZENTRALINSTITUT FUER ORGANISCHs patent filings in countries
# Country Total Patents
#1 Germany 20
#2 German Democratic Republic 2

Patent filings per year

Chart showing ZENTRALINSTITUT FUER ORGANISCHs patent filings per year from 1900 to 2020

Top inventors

# Name Total Patents
#1 Forkel Klaus Dr 3
#2 Vollhardt Dieter Dr 3
#3 Krause Hanswalter Prof Dr 3
#4 Andreae Siegfried Dr 2
#5 Hermel Horst Dr 2
#6 Oehme Guenther Prof Dr 2
#7 Wulf Jens-Peter 2
#8 Schmitz Ernst Prof Dr 2
#9 Tomaschewski Georg Prof Dr 2
#10 Foken Heinrich 2

Latest patents

Publication Filing date Title
DE4143287A1 Prodn. of 2-aryl-cyclo-hex-2-en-3-ol-1-one herbicides and miticides - comprises reacting 3-aryloxy-cyclo-hex-2-en-1-one with potassium carbonate and treating with acid
DE4142247A1 Selective catalytic co-cyclisation of acetylene and nitrile(s) to pyridine derivs. - by photochemical conversion in soln. under inert gas atmos. using cobalt complex catalyst
DE4140928A1 Herbicide esp. for controlling weeds in beet crops - contains carbamate active ingredient, solvent mixt. comprising water-soluble and oil-soluble solvent crystallisation inhibitor and emulsifier
DE4133145A1 Prepn. of new propranolol analogues - by reacting racemic oxirane(s) with optically active amine(s), then selective oxidn., useful in regulation of blood pressure
DE4133143A1 New diastereomeric propranolol analogues - e.g. 1-(1-naphthyl:oxy)-3 -(1-phenyl:ethylamino) -propan-2-ol cpd., used to regulate blood pressure without affecting heart rate
DE4132747A1 Polyurethane-urea solns. prepn. having defined, reproducible viscosity - involves reacting di:isocyanate diol(s) and di:functional chain extender contg. amino-acidic pyrazole
DE4130078A1 Protein modified composite contg. cement, polymer and glass fibres - comprises aq. soln. of protein and hardener, for high mechanical and chemical properties in building industry
DE4130077A1 Coating compsn. for glass fibres - comprising aq. protein soln. e.g. casein contg. hardener e.g. aliphatic aldehyde, for improved resistance to aggressive media e.g. acid
DE4130076A1 Cement-based composite material for fibre-free construction material - contg. poly:di:methyl:di:allyl ammonium chloride, improving refractory properties
DE4128796A1 Electron beam negative resist developed by aq. alkali - contg. 4-halophenol novolak and poly:cyclic partly hydrogenated triazine deriv. as crosslinker
DE4122733A1 Image reversal resist used to produce reverse resist - contains naphthoquinone di:azide cpd., oligomer of oxa:cycloalkane as crosslinker and novolak or polyvinyl-phenol] resin binder
DE4122732A1 Potential side-chain liq. crystal acrylate monomers prepn. - by reaction of 4-hydroxybenzoic acid with 4-alkoxyphenol or bisphenol then with di:bromo:alkane and then with alkali (meth)acrylate
DE4121959A1 Supported catalyst for acetic acid prodn. by carbonylation of methanol - with phosphonic acid deriv. contg. dissimilar chelating gps. as adhesion promoter
DE4114237A1 Kinetic racemate sepn. of chiral organic hydroperoxide(s) - by using the hydro-peroxide in Sharpless epoxidation of allyl alcohol and isolating the enantiomer which reacts more slowly
DE4114238A1 Substd. 2,2-penta:methylene-delta -3-imidazolin-5-one derivs. - for the construction and modification of biologically active cpds.
DE4114236A1 Prepn. of substd. glycinamide derivs. - by reacting substd. acetonitrile with 3,3-penta:methylene oxaziridine in the presence of an auxiliary base
DE4112111A1 Optically active 3,4-di:substd. pyrrolin-2,5-di:one derivs. - for use as chiral N-contg. ligands with transition metals to form catalytic systems for asymmetric catalyses
DE4108345A1 New 5-amino-4-di:alkoxy:phosphoryl-oxazole derivs. - prepd. by reacting phosphonate salt with amine, are useful as fungicides
DE4103759A1 METHOD FOR PRODUCING (S) - AND (R) -ALPHA-AMINOSAUR DERIVATIVES BY ASYMMETRIC HYDRATION
DE4103450A1 Pilot plant for small scale simulation of hydrocarbon cracking plant - enables direct transfer of performance results to full scale