"Rail travel at high speeds is not possible because passengers, unable to breathe, would die of asphyxia."
Dionysius Lardner, Professor of Natural Philosophy and Astronomy at University College, London ; 1830
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| Number | Title | Issue Date |
| 7256298 | Pyrazole derivatives and process for the production thereof The present invention provides pyrazole derivatives useful as production intermediates for isoxazoline derivatives having an excellent herbicidal effect and selectivity between crops and weeds as well as processes for producing the same. The pyrazole derivati... | 08/14/2007 |
| 7227043 | 2-phenyl-2-substituted-1,3-diketones The invention relates to novel phenyl-substituted cyclopentane- and cyclohexane-1,3-dione derivatives of the formula (I) in which W, X, Y, Z, A, B, Q1, Q2, Q3 | 06/05/2007 |
| 7214701 | Active substance combinations having insecticidal and acaricdal properties The invention relates to insecticidal mixtures for protecting plants against attack by pests comprising (a) compounds of the formula (I) ... | 05/08/2007 |
| 7205289 | Combinations of active ingredients with insecticidal and acaricidal properties The invention relates to novel active compound combinations of certain cyclic ketoenols and certain insecticidally active compounds that together have very good insecticidal and acaricidal properties. ... | 04/17/2007 |
| 7183238 | [1,2]-oxazine-3,5-diones The present invention relates to novel [1,2]-oxazine-3,5-dione derivatives of the formula (I) in which W, X, Y, Z, G, D, A and B are as defined in the disclosure, to a pl... | 02/27/2007 |
| 7109228 | Pyrazole derivatives This invention relates to pyrazole derivatives of formula (I) or pharmaceutically acceptable salts, solvates or derivatives thereof, and to processes for the preparation thereof, intermediates used in their prepa... | 09/19/2006 |
| 7105471 | Arylphenyl-substituted cyclic ketoenols The present invention relates to novel arylphenyl-substituted cyclic ketoenols of the formula (I) in which X represents halogen, alkyl, alkoxy, alkenyloxy, alkylthio, alkylsulph... | 09/12/2006 |
| 6987104 | Pyrrolidine bicyclic compounds and its derivatives, compositions and methods of use N-[1-oxo-(optionally 2-aza)-2-alkyl-3-(carboxyl or thiol or hydroxyaminocarbonyl or N-hydroxyformamido)-propyl]-(aryl or heteroaryl)-azacyclo4-7alkanes or thiazacyclo4-7alkanes, salts or prodrugs thereof have interesting properties, e.g., in th... | 01/17/2006 |
| 6894005 | Herbicides Compounds of formula wherein the substituents have the meanings given in claim 1, and agronomically tolerable salts, isomers and enantiomer of those compounds, are suitable for use as herbicides. ... | 05/17/2005 |
| 6852749 | Pyrazolidinol compounds The invention provides the use of an optionally hydroxy-protected 4-hydroxyo or hydroperoxy-3,5-dioxopyrazolidine or an equivalent wherein a pyrazolidine ring attached oxygen is replaced by a sulphur, or a physiologically acceptable salt thereof, for the manufacture... | 02/08/2005 |
| 6686318 | Heterocyclically substituted aromatic amino compounds with a herbicidal effect The invention relates to new substituted aromatic amino compounds of the general formula (I) ##STR1## in which R1, R2, R3, R4 and Z have the meanings given in the description, to a process for their preparation,... | 02/03/2004 |
| 6576632 | Biaryl compounds useful as anticancer agents The present invention relates to compounds of formula I ##STR1## and to pharmaceutically acceptable salts, hydrates and prodrugs thereof, wherein R1, R2, R3, R4, R5, R10, R11, b,... | 06/10/2003 |
| 6551360 | Pyrazoline-3,5-dione-containing compositions for dyeing keratin fibres; their use in dyeing as couplers; dyeing process The present invention relates to a composition for dyeing keratin fibres, in particular human hair, containing, in a medium which is suitable for dyeing: as coupler, at least one compound of formula: ##STR1## or one of the addition salts thereof with an a... | 04/22/2003 |
| 6458474 | Methine compound, material for organic luminescence element, organic luminescence element using the same Disclosed is a novel methine compound, for example, which is represented by the following formula (I): ##STR1## wherein R1, R2, R3, R4 and R5 each represents a hydrogen atom or a substituent; X repres... | 10/01/2002 |
| 6451790 | Azadioxacycloalkenes and their use for combating harmful fungi and animal pests Compounds of formula I ##STR1## wherein W is optionally substituted alkylene; Y is N or CRa ; Ra is hydrogen, halogen or alkyl; R1n represents hydrogen or 1 to 4 substituents; R2 is hydrogen, nitro, cyano, halo... | 09/17/2002 |
| 6331537 | Carboxylic acids and carboxylic acid isosteres of N-heterocyclic compounds This invention relates to novel N-heteorocyclic carboxylic acids and carboxylic acid isosteres, their preparation and use for treating neurological disorders including physically damaged nerves and neurodengenerative diseases, for treating alopecia and pr... | 12/18/2001 |
| 6322775 | Cosmetic compositions containing pyrazolin-4,5-diones, novel pyrazolin-4,5-diones, preparation methods therefor and uses thereof The present invention relates to novel cosmetic compositions, in particular for coloring the skin and/or the hair, comprising, in a cosmetically acceptable support, at least one 4,5-pyrazolinedione. The invention also relates to novel 4,5-pyrazolinediones... | 11/27/2001 |
| 6180568 | 4-aryl-4-substituted pyrazolidine-3, 5-dione derivatives A 4-aryl-4-substituted pyrazolidine-3,5-dione derivative represented by the formula (1) is useful as an effective component of a miticide, insecticide or herbicide ##STR1## wherein R1 and R2 are each independently alkyl group having ... | 01/30/2001 |
| 6057354 | Pesticidal 1-arylpyrazoles 1-Arylpyrazoles of the formula: ##STR1## wherein R31, R32, R33, R4, R5, R12, R13, R14, R15 and Z are as defined in the specification, are useful as pes... | 05/02/2000 |
| 6015911 | Process for preparing 1-alkyl-4-(2-chloro-3-alkoxy-4-alkylsulfonylbenzoyl)-5-hydroxypyrazole and related compounds Herbicidal 1-alkyl-4-(2-chloro-3-alkoxy-4-alkylsulfonylbenzoyl)-5-hydroxypyrazole compounds, as well as 1-halo-2-chloro-3-alkoxy-4-alkylsulfonylbenzene compounds and 2-chloro-3-alkoxy-4-alkylsulfonylbenzoic acid compounds, were prepared in good yield... | 01/18/2000 |
| 5994274 | Dialkyl phenyl halide-substituted keto-enols for use as herbicides and pesticides The present invention relates to new compounds of the formula (I) ##STR1## in which X represents alkyl, Y represents halogen or alkyl and Z represents halogen or alkyl, with the proviso that one of the radicals Y and Z always represents halogen and the ot... | 11/30/1999 |
| 5958382 | 4,4-dihydroxy-5-pyrazolinones and cosmetic/dermatological compositions comprised thereof Novel 4,4-dihydroxy-5-pyrazolinones having the structural formula (I): ##STR1## and cosmetic/dermatological formulations comprised thereof are useful for artificially coloring, e.g., tanning/browning, human skin and/or hair, and are well suited for i... | 09/28/1999 |
| 5763618 | Manufacturing method of sulfides A method of manufacturing a sulfide comprises the steps of (a) dissolving a thiol in a solvent to form a solution; (b) oxidizing the thiol to a disulfide in the presence of a first oxidizing agent in the solution; (c) reacting the disulfide with a coupler... | 06/09/1998 |
| 5739083 | Pyrazole derivatives and insecticidal compositions containing the derivative as active component A pyrazole derivative represented by the formula (1) is low in toxicity and persistence and yet has an extremely high insecticidal efficacy ##STR1## wherein A is CH, N or C-halogen atom, R1 is hydrogen atom, lower alkyl, lower haloalkyl, b... | 04/14/1998 |
| 5719292 | Process for preparing a thioether compound The invention provides a process for preparing a coupler compound having a thioether group at the coupling site comprising reacting in the presence of a base (a) a coupler compound having at least one hydrogen at the coupling site with (b) a mixed disulfi... | 02/17/1998 |
| 5712303 | Pyrazoles and pyrazolopyrimidines having CRF antagonistic activity The pyrazoles and pyzazolopyrimidines of the formula ##STR1## wherein R1, R2, R3, R4 and A are as defined herein, have corticotropin releasing factor (CRF) antagonist activity. As such, they are effective i... | 01/27/1998 |
| 5707936 | Methyl -phenylbutenoates Methyl -phenylbutenoates of the formula I ##STR1## where -- is a single or double bond and the index and the substituents have the following meanings: n is 0, 1, 2, 3 or 4; R1 is nitro, cyano, halogen, alkyl, haloalkyl or alkoxy; R2... | 01/13/1998 |
| 5646297 | Process for preparation of 2-equivalent 4-arylthio-5-pyrazolone magenta couplers A process for preparation of 2-equivalent 4-arylthio-5-pyrazolone magenta couplers comprises the steps of: (i) reacting a 4-equivalent 5-pyrazolone magenta coupler and a diaryldisulfide compound in the presence of 1,8-diazabicyclo-[5,4,0]-undecen-7-ene an... | 07/08/1997 |
| 5631381 | Process for the preparation of pesticidal 1-(haloaryl) heterocyclic compounds Process for preparing complex pesticidal 1-(haloaryl)heterocyclic compounds by reacting 1-(nitroaryl)heterocycles with metallic halide salts.... | 05/20/1997 |
| 5618775 | Mixtures of optically active cyclohexenone oxime ethers, their preparation, intermediates for this purpose and their use as herbicides Mixtures of optically active cyclohexenone oxime ethers having R- and S-configuration in the oxime ether moiety of the formula I ##STR1## (R1 =C1 -C6 -alkyl; ##STR2## X=C1-C.sub.4 -alkyl, C1... | 04/08/1997 |
| 5574169 | Substituted pyrazolidin-3-one derivatives The present invention provides an enantiomerically selective process and intermediates for preparing certain 4,5-disubstituted pyrazolidinones and intermediates which are useful for treating diseases of the central nervous system.... | 11/12/1996 |
| 5523280 | Phenylpyrazole fungicides Phenylpyrazoles of the formula: ##STR1## in which: X.dbd.H, hal, NO2, CN, SCN, alkyl (C1 -C4), alkenyl (C2 -C4), alkynyl (C2 -C4), alkoxy (C1 -C4), alk... | 06/04/1996 |
| 5506193 | Herbicidally, acaricidally and insecticidally active pyrazolidine compounds The present invention relates to herbicidally, acaricidally and insecticidally active pyrazolidine-3,5-diones of the formula I ##STR1## in which R1 is ##STR2## R2 and R3 independently of one another are C1 | 04/09/1996 |
| 5474974 | 3-hydroxy-4-aryl-5-oxo-pyrazoline derivatives There are provided new 3-hydroxy-4-aryl-5-oxo-pyrazoline derivatives of the formula (I) ##STR1## The new 3-hydroxy-4-aryl-5-oxo-pyrazoline derivatives of the formula (I) have a particularly pronounced activity against animal pests, in particular... | 12/12/1995 |
| 5424280 | Aryloxybenzene herbicidal agents There are provided aryloxybenzene compounds of formula I ##STR1## Further provided are compositions and methods comprising those compounds for the control of undesirable plant species.... | 06/13/1995 |
| 5399708 | Pyrazolidin-3-one derivatives The present invention provides an enantiomerically selective process and intermediates for preparing certain 4,5-disubstituted pyrazolidinones and intermediates which are useful for treating diseases of the central nervous system.... | 03/21/1995 |
| 5283337 | Process for the preparation of perhaloalkylthioethers The present invention relates to a process for the preparation of perhaloalkylthioethers by bringing a perhaloalkyl halide, preferably a bromide or an iodide, into contact with a disulphide in the presence of zinc and of sulphur dioxide or of a dithionite... | 02/01/1994 |
| 5202442 | Process for preparing pyrazolecarboxylic acid compounds A process for preparing a pyrazolecarboxylic acid compound of the formula (II): ##STR1## wherein Y and Z each represent a hydrogen, a halogen, a nitro, a cyano, COOR1, NR1 R2, CONR1 R2, SR1 | 04/13/1993 |
| 5185025 | Substituted pyrazoles and their use as herbicides The present invention relates to certain novel substituted 3-phenoxypyrazoles and their use as herbicides.... | 02/09/1993 |
| 5183825 | 4-arylmethyl-5-alkyl-3H-pyrazol-3-ones and hypoglycemic use The compounds of the formula: ##STR1## in which the dotted lines represent optional unsaturation when X is CR5, Y is CR6 or X or Y are N; R1 is hydrogen, alkyl, aryl or arylalkyl; R2 is hydrogen, alkyl, ary... | 02/02/1993 |