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Class 560/54 - Polycarboxylic acid


Subclass of Class 560 - Organic compounds -- part of the class 532-570 series
Definition: Compounds wherein the acid radical contains more than one
No. of patents: 79
Last issue date: 05/06/2008


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NumberTitleIssue Date
7368566Process and intermediates for preparing benzazepines
Disclosed is a new process and intermediates for preparing benzazepines of Formula (I): wherein R1 and R2 are as defined herein. ...
05/06/2008
7361335Methods for using an elastase
The invention provides methods for treating an obstructed biological conduit that include administering to the conduit an agent that can degrade extracellular matrix of obstructing tissue. Particular methods include delivery of an enzyme or a mixture of several enzy...
04/22/2008
7339071Aryl ethynyl phthalic acid derivative and method for producing the same
The invention provides an aryl ethynyl phthalic acid and derivatives thereof (including fluorine-containing compounds) represented by Formulae 1, 3, 5, 4A and 5A including the structure of Formula 2, and method of producing these compounds, in which an aryl ethynyl ...
03/04/2008
7129367Phosphine compound, its intermediate, its complex with palladium and a manufacturing method of unsaturated compounds by using the palladium complex
Palladum-phosphine complexes obtained by reacting a 5 compound of formula (1) below with a palladium compound: F(I) (wherein R1 is a hydrogen atom, an alkyl group, a cycloalkyl group or a phenyl group which may be substituted; R2 and R3
10/31/2006
6878845Oligomers from multifunctional acrylates
Oligomers from multifunctional acrylates and organonitro compounds are provided. Films obtained from crosslinked oligomers of the present invention are useful as protective or decorative coatings as well as components in adhesives and composites. ...
04/12/2005
6743941Process for the production of piperidine derivatives
The present invention relates to processes for preparing certain piperidine derivatives, including fexofenadine (F), the active ingredient in the non-sedating antihistamine sold in the U.S. under the designation “Allegra®”. This invention also relates to novel ...
06/01/2004
6569810Cyclopentane-1,3-dione derivatives
The present invention relates to novel bicyclic cyclopentane-1,3-dione derivatives of the formula (I) ##STR1## to a process for their preparation and to their use as pesticides and herbicides....
05/27/2003
6509374Compounds, their preparation and use
The present invention relates to compounds of the general formula I. The compounds are useful in the treatment of conditions mediated by nuclear receptors, in particular the Peroxisome Proliferator-Activated Receptors (PPAR)....
01/21/2003
6441218Process for producing 2-substituted propionic acid
Adipic acid diester is caused to react with alkoxide M(OR)n, wherein R is an alkyl group and M is an alkali metal or alkaline earth metal, the reaction product is successively subjected either to coupling with halomethylstyrene followed by carb...
08/27/2002
6369026Slow release of fragrant compounds in perfumery using 2-benzoyl benzoates, 2-alkanoyl benzoates or alpha-keto esters
The present invention describes a fragrance delivery system which releases fragrant alcohols upon exposure to light. Said system comprises 2-benzoyl benzoates of general formulae ##STR1## which can comprise various subtituents R1 -R5...
04/09/2002
6337034Vinylene compounds and liquid-crystal composition
Liquid crystalline compounds which have a wide temperature range of liquid crystal phase, low viscosity, and improved threshold voltage; liquid crystal compositions; and liquid crystal display devices comprising the composition can be provided; and the li...
01/08/2002
6335462Polymerizable oligomesogenes
The compounds of the formula I X[--Y1 --A1 --Y2 --M--Y3 --A2 --Z]n I, wherein the variables are as defined in the specification. The compounds are suitable as alignment layers for liquid-crystalline ...
01/01/2002
6258977Alkyl3-oxoalkanoates
An alkyl 3-oxoalkanoate, a process for preparation and use for the synthesis of fatty hydroxylated amino acids, fatty amino alcohols and ceramides....
07/10/2001
6133228Slow release of fragrant compounds in perfumery using 2-benzoyl benzoates, 2-alkanoyl benzoates or ଱-keto esters
A fragrance delivery system which releases fragrant alcohols upon exposure to light. The system comprises 2-benzoyl benzoates of general formulae ##STR1## which can comprise various subtituents R1 -R5 as defined in the applicati...
10/17/2000
5952386Dihalopropene compounds, insecticides containing them as active ingredients, and intermediates for their production
The present invention provides dihalopropene compounds of the general formula: ##STR1## wherein R1 is C1 -C10 alkyl or the like; L is C(.dbd.O)NH or the like; R2, R3 and R4 are indepen...
09/14/1999
5852200Cross-coupling of organic compounds using cuprous iodide
Cross-coupling or addition reactions of organic compounds, including acid halides, allylic halides, and ଱,ଲ-unsaturated carbonyl containing compounds, with organozinc compounds may be readily and safely carried out in the presence of cuprous i...
12/22/1998
5739376Fullerene derivatives, methods of preparing them and their use
Fullerene derivatives, methods of preparing the same and methods of using the same, wherein the fullerene derivatives are of the formula I ##STR1##...
04/14/1998
5723648Intermediates for anti-microbial benzoheterocyclic compounds
Novel 4-oxoquinoline-3-carboxylic acid compounds of the formula: ##STR1## wherein R1 is cyclopropyl which may have 1 to 3 substituents of alkyl and halogen; phenyl which may be substituted by 1 to 3 substituents of alkoxy, halogen and OH; ...
03/03/1998
5523476Processes for producing tetrafluorophthalic anhydride and fluorobenzoic acids
A process for producing tetrafluorophthalic anhydride, which comprises chlorinating tetrachlorophthalic anhydride to obtain 3,3,4,5,6,7-hexachloro-1-[3H]-isobenzofuranone, then fluorinating it to obtain 3,4,5,6-tetrafluorophthaloyldifluoride and/or 3...
06/04/1996
5457124Carboxylic acid Leukotriene B4 antagonists
The invention relates to compounds selected from the group consisting of the formulas: ##STR1## wherein R2 and Ph are as described herein. These compounds are potent leukotriene B4 antagonists and are therefore useful in the tre...
10/10/1995
5434186Carboxylic acid leukotriene B4 antagonists
Compounds of the formula ##STR1## wherein X is O or CH2 ; Y is O, --CH2 --CH2 --, --CH.dbd.CH--, --C.tbd.C--, or --OCH2 C6 H4 --; Z is --CH2 --CH2 --, --CH.dbd.CH-- or...
07/18/1995
5403952Substituted cyclic derivatives as novel antidegenerative agents
Novel substituted cyclic compounds of Formula I are found to be useful inhibitors of matrix metalloendoproteinase-mediated diseases including osteoarthritis, rheumatoid arthritis, septic arthritis, tumor invasion in certain cancers, periodontal disease, c...
04/04/1995
5389619Derivatives of phenylacetic acid, their preparation and their use as pesticides
Compounds of the formula I ##STR1## where n, W, X, Y, Z, R1, R2, and R3 are as defined herein exhibit fungicidal, insecticidal, and acaracidal activity....
02/14/1995
5359125Thermosetting coating compositions
Disclosed are certain novel 2,2'-bisacetoacetates useful as crosslinking agents and a process for the preparation therefor. Also provided are novel enamel compositions containing the crosslinkers and coatings and articles coated with thermosetting coating...
10/25/1994
5350872Process for the preparation of carboxylic acids and derivatives of them
The subject matter of the invention is a process for the preparation of carboxylic acids and derivatives of them of the general formula ##STR1## wherein R means hydrogen, or a C1-4 alkyl or a (C1-5 alkoxy)carbonyl group, R1...
09/27/1994
5322794Fluorescent phospholipid analogs and fatty acid derivatives
Fluorescence probes are described comprising coronene fluorophores chemically attached to lipids or membrane-mimetic molecules via hydrocarbon spacers of defined length. Also described is a method for determining lipid packing and dynamics in membranes, a...
06/21/1994
5196564Physiologically active substance TAN-931, its derivatives, their production and use
A novel compound of the formula (I): ##STR1## wherein R1 is esterified carboxyl; R2, R3 and R4 are the same or different and are hydrogen or alkyl; A is formyl, hydroxyiminomethyl or carboxyl; and X is hydr...
03/23/1993
5191108Catechol carboxylic acids
The invention relates to catechol carboxylic acid derivatives of the formula ##STR1## wherein, R1 is ##STR2## acetyl, hydrogen, hydroxy or alkanoyloxy, R2 is ##STR3## hydroxy, hydrogen or alkanoyloxy, wherein R ...
03/02/1993
5136081Process for the preparation of cyclopentene, cyclopentane and cyclohexane derivatives
The invention provides a process for the preparation of fungicidally active cyclopentene derivatives of the general formula ##STR1## cyclopentane derivatives of the general formula ##STR2## and cyclohexane derivatives of the general formula ...
08/04/1992
51240833-substituted and 3,3-disubstituted 4-oxoretinoic acids and their esters
There are disclosed 3-substituted and 3,3-disubstituted all-trans-4-oxoretinoic acids and 3-substituted and 3,3-disubstituted 13-cis-4-oxoretinoic acids and their lower alkyl esters....
06/23/1992
5081308Ultraviolet radiation absorbing compositions of bis-1,3-diketone derivatives of cyclohexane
Sunscreen compositions are described which contain certain bis-1,3-diketone derivatives of cyclohexane when incorporated in a carrier in amounts ranging from 0.1-50% by weight....
01/14/1992
5051527Liquid crystal compounds having fluoroalkyl radical
The invention lies in novel ferroelectric liquid crystal compounds particularly represented by the general formulae, having a good responsibility in relation to the applied electric field and a wide range of phase transition points inclusive of the room t...
09/24/1991
5041638Alkenoic acid derivatives
An alkenoic acid derivative of the formula ##STR1## in which X and Y are identical or different and represent sulfur, sulfoxide, sulfone, an alkylene chain, --SCH2 --, or oxygen or a direct bond, W represents --CH.dbd.CH-- or --CH2
08/20/1991
5039672Heterocyclic compounds as aldose reductase inhibitors
Certain spirocyclic heterocyclic compounds, and their pharmaceutically-acceptable salts, are inhibitors of the aldose reductase enzyme, and so are useful for the control of diabetic complications. Exemplary compounds include compounds of the formula ...
08/13/1991
5039308Multifunctional fuel additives
Additives which improve the low-temperature properties of distillate fuels are the reaction products of (1) diaminodiols, and (2) the product of benzophenone tetracarboxylic dianhydride and aminoalcohols and/or amines with long-chain hydrocarbyl groups at...
08/13/1991
4997973Ortho-substituted benzyl carboxylates and fungicides containing these compounds
Benzyl carboxylates of the formula ##STR1## where R1 is alkyl, R2 is hydrogen, alkyl or alkoxy, R3 is hydrogen, halogen, cyano, aryl or aryloxy, the aromatic ring being unsubstituted or substituted, or R3 is het...
03/05/1991
4997591Chiral smetic liquid crystals and glassy materials containing the same for displaying and storing information
The chiral smetic liquid-crystalline compounds of the general formula (I) M1.sup.* --B--M2.sup.* (I) solidify on cooling from the liquid-crystalline phase in glassy form, as a result of which they are suitable for mat...
03/05/1991
4994610Process for preparing fluorinated benzoyl compounds
Fluorinated benzoyl compounds of the formula: ##STR1## wherein Q is a lower alkyl group, a halogen atom, --CH2 CO2 R1 wherein R1 is a lower alkyl group, or ##STR2## wherein each of R2 and R
02/19/1991
4894181Carbocyclic compounds
Carbocyclic compounds of the formula I ##STR1## wherein Q is a benzene or cyclohexane ring or a naphthalene system, X is in each case --CH2 --(CH2)p -- where it is also possible for one or two non-adjacent CH2
01/16/1990
4889947Ultraviolet radiation absorbing naphthalenylidene compositions
Sunscreen compositions are described which contain certain substituted naphthalenylidenes which act as UV filters when incorporated in a carrier in amounts ranging from 0.1-50% by weight....
12/26/1989
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