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A personal computer peripheral, battery powered reward candy dispenser which immediately presents students with a single candy for each problem completed correctly.
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| Number | Title | Issue Date |
| 5352654 | Pyridyl sulfonylurea herbicides N-Pyridinesulfonyl-N'-pyrimidinyl- and -triazinylureas of the formula I ##STR1## in which R1 is hydrogen, halogen, C1 -C4 alkyl, C1 -C4 alkoxy, C1 -C4 alkylthio, C1 C | 10/04/1994 |
| 5336773 | Certain-3-amino-2-pyridine-sulfonamide intermediates N-Pyridinesulfonyl-N'-pyrimidinyl- and -triazinylureas of the formula I ##STR1## in which R1 and R2 independently of one another are hydrogen, C1 -C8 alkyl or C3 -C8 cycloalkyl; C2 | 08/09/1994 |
| 5332806 | Disazo dyes which contain 2-hydroxynaphthyl moiety Azo dyes of the formula ##STR1## where A and B are each independently of the other substituted or unsubstituted phenyl or naphthyl and X is --N(R1)--SO2 --, --O--SO2 -- or --SO2 --N(R1)--, where ... | 07/26/1994 |
| 5328995 | Azo dyes containing triazine middle components and a 1,4-phenylene-2,5-disubstituted coupling component The compounds of the formula ##STR1## where the substituents are as defined in claim 1, are direct dyes for various substrates, in particular cellulosic fibre materials. They are high temperature resistant and therefore are particularly highly suitab... | 07/12/1994 |
| 5324330 | Dye mixtures and the use thereof Dye mixtures comprising at least one dye of formula ##STR1## and at least one dye of formula ##STR2## wherein the substituents are as defined in claim 1, have good allround fastness properties and are suitable for dyeing cellulosic fibre ma... | 06/28/1994 |
| 5324763 | Agent for the treatment of fibre materials Highly effective agents for the water and oil repellent finishing of fibrous, in particular textile materials contain at least two components which are aqueous dispersions. One of the dispersions contains a copolymer of a fluorine-containing (meth)acrylat... | 06/28/1994 |
| 5320785 | Compositions containing phosphono compounds and organic acids as flameproofing agents The permanence of the flame-resistant finish of fibre materials, in particular those based on cellulose, is improved if a phosphono compound which contains an N-methylol group. is used together with an organic carboxylic acid as the finishing agent. If ox... | 06/14/1994 |
| 5310721 | Process for the preparation of microcapsules using a salt of a partial ester of a styrene-maleic anhydride copolymer This invention relates to a process for encapsulation and particularly for the preparation of microcapsules having a capsule wall of a solid polymeric substance enclosing a water-immiscible material, which process comprises preparing a solution of a first... | 05/10/1994 |
| 5310783 | Aqueous compositions comprising nitrogen-containing polysiloxanes Stable, low-viscosity dispersions of polysiloxanes containing amino or amido groups can be obtained, even at comparatively high concentrations and/or pH values, by adding a product of the formula R1--CH(X)--Y--O--R2 (R1 is H, CH3 ; X=OH, NH2 | 05/10/1994 |
| 5308545 | Pyrazoline compounds The invention relates to pyrazoline compounds of formula ##STR1## wherein R1 is hydrogen or methyl, R2 and R3 are each independently of the other methyl, ethyl or hydroxyethyl, R4 is hydrogen or chlorine, R... | 05/03/1994 |
| 5308819 | Diphosphines containing silane groups, immobilised diphosphines and the use thereof as hydrogenation catalysts Compounds where a solid carrier material which contains diphosphine rhodium or iridium complexes fixed on the surface thereof, of which the carrier material has the formula IV or IVa: ##STR1## wherein Y denotes two monoolefin ligands or a diene ligan... | 05/03/1994 |
| 5302704 | Azodyes containing a sulfoacetoacetic acid anilide coupling component Dyes of formula ##STR1## wherein D is the radical of a diazo component of the benzene or naphthalene series or of the heterocyclic series, R1 is hydrogen or C1 -C4 alkyl and R2 is phenyl or substituted phen... | 04/12/1994 |
| 5298036 | Mixture of disazo dyes containing sulfo-substituted 1,4-naphthalene middle components Azo dyes of the formula ##STR1## in which R1 and K are as defined in claim 1, produce on nitrogen-containing or hydroxyl-containing fibre materials dyeings having good fastness properties.... | 03/29/1994 |
| 5296449 | Synergistic composition and method of selective weed control Herbicidal composition comprising 5-(2,4,6-trimethylphenyl)-2-[1-(ethoximino)propionyl]-cyclohexane-1,3-dion e of formula I ##STR1## and a synergistically effective amount of either 2-[4-(5-chloro-3-fluoropyridin-2-yloxy)phenoxy]-propionic acid p... | 03/22/1994 |
| 5288868 | Process for the preparation of 2-hydroxy-4,6-diaryl-1,3,5-triazine There is disclosed a process for the preparation of 2-hydroxy-4,6-diaryl-1,3,5-triazines by reacting an aromatic nitrile with an alkali metal amide and an alkyl haloformate, using an equimolar amount of each, which process is carried out as a one-pot synt... | 02/22/1994 |
| 5288858 | Diazo dyes containing a hydroxy alkoxybenzene middle component and a pyrazole coupling component The invention relates to azo dyes of the formula ##STR1## in which R, R1 and R2, independently of one another, are hydrogen, substituted or unsubstituted C1 -C8 alkyl or phenyl, R3 is hydrogen or... | 02/22/1994 |
| 5270455 | Polyazo dyes containing resorcinol as middle component and metal complexes thereof A metal complex suitable as dyes for the dyeing of a wide range of textile and non-textile materials, particularly leather and fur, said metal complex of a compound of the formula ##STR1## in which D and D1, independently of one another, a... | 12/14/1993 |
| 5268475 | Triphene dioxazine dyestuffs The compounds of formula (1) are suitable for use as direct dyes for dyeing and printing a wide range of materials, especially cellulosic fibers, to give dyeings and prints of good all-round fastness properties: ##STR1## wherein R and R1 a... | 12/07/1993 |
| 5264000 | Aqueous solutions of synthetic tanning agents Aqueous solutions of synthetic tanning agents comprising (A) a lithium salt of a synthetic, anionic aromatic tanning agent or the anionic non-condensed precursor thereof, and, as optional components, (B) a water-soluble chromium, aluminum, iron or zirconium salt or... | 11/23/1993 |
| 5252751 | Diphosphines containing silane groups, immobilised diphosphines and the use thereof as hydrogenation catalysts Compounds of formula I ##STR1## wherein R1 denotes identical or different radicals and is linear or branched C1 -C12 alkyl, unsubstituted C5 -C6 cycloalkyl or C5 -C6 cycloal... | 10/12/1993 |
| 5245040 | Process for the preparation of nitroguanidine derivatives A process for the preparation of 1,3-disubstituted 2-nitroguanidines of the formula I ##STR1## in which R1 is hydrogen or C1 -C4 alkyl, R2 is hydrogen, C1 -C6 alkyl, C3 -C | 09/14/1993 |
| 5244857 | Diphosphines containing silane groups, immobilise diphosphines and the use thereof as hydrogenation catalysts Compounds of formula II ##STR1## wherein the groups (R1)2 P(CH2)m and n are in o- or m-position to each other and the substituents R1 are identical or different radicals, m and n are each indepen... | 09/14/1993 |
| 5241054 | Cationic azo dyes The novel azo dyes of formula I as indicated in claim 1 are suitable for dyeing and printing, especially paper of all kinds.... | 08/31/1993 |
| 5237084 | Preparation of dialkyl (N-cyanoimido)carbonates from dialkyl imidocarbonates and cyanogen halides Dialkyl (N-cyanoimido) carbonates are prepared in good yield in a non-aqueous solvent by a process which comprises either (a) adding a cyanogen halide at a controlled rate to a reactor containing an unsubstituted or substituted dialkyl imidocarbonate, an ... | 08/17/1993 |
| 5233026 | Azo dyes containing chloro-s-triazine and vinylsulfonyl type fiber-reactive groups Reactive dyes of the formula ##STR1## in which D is a monoazo dye, R1 is hydrogen or a substituted or unsubstituted C1-4 alkyl radical, Z is an unsubstituted or substituted amino group, and X is a vinyl, ଲ-sulfatoethyl, ... | 08/03/1993 |
| 5230803 | Ground- and wastewater purification There is disclosed a process for purifying ground- and wastewaters, which comprises subjecting said waters to a membrane separation process between a biological treatment step and adsorption on activated carbon.... | 07/27/1993 |
| 5229507 | Substituted naphthalocyanines and their use Compounds of the formula I ##STR1## in which R is the group --OCm H2mn R1 and M is two H or is Cu or Ni, R1 is --OH, --Cl, --Br, C1 -C30 alkoxy or --OC(O)R2, m is an integer... | 07/20/1993 |
| 5223520 | Pyridine compounds which are useful as pesticides Compounds of formula ##STR1## wherein R1 is hydrogen, C1 -C4 alkyl or C3 -C6 cycloalkyl, R2 is hydrogen or C1 -C4 alkyl, R3 is hydrogen, C1 ... | 06/29/1993 |
| 5223177 | Alkali-resistant foam suppressant which is free from silicone oil Alkali-resistant foam suppressant which is free from silicone oil, containing (a) a homopolymer of an aliphatic C2 -C12 alkyl ester of (meth)-acrylic acid or a copolymer of this alkyl ester with a di-C2 -C12 alk... | 06/29/1993 |
| 5223018 | 1-phenyl-piperdine-2,6-diones with herbicidal activity The invention relates to new 1-phenyl-piperidine-2,6-diones of the formula I ##STR1## wherein R is C3 -C7 -cycloalkyl, R1 is hydrogen or halogen; R2 is hydrogen, cyano, nitro or halogen; and A is hydrogen, cyano... | 06/29/1993 |
| 5223626 | Preparation of cationic alkylenediamine dye intermediates Compounds of the formula ##STR1## where R1, R2 and R3 are each independently of the others hydrogen, C1 -C4 alkyl, C1 -C4 alkoxy, halogen or C1 -C4 alk... | 06/29/1993 |
| 5221315 | Sulfonylureas N-Pyridinesulfonyl-N'-pyrimidinyl- and -triazinylureas of the formula I ##STR1## in which R1 and R2 independently of one another are hydrogen, C1 -C8 alkyl or C3 -C8 cycloalkyl; C2 | 06/22/1993 |
| 5220062 | Process for the preparation of benezenesulfonamides There is disclosed a multi-step process for the preparation of benzenesulfonamides of general formula ##STR1## wherein R is 3,3-difluorobutyl or 3,3-difluorobuten-1-yl. The benzenesulfonamides obtainable by the process of the invention are inter... | 06/15/1993 |
| 5218021 | Compositions for polar solvent fire fighting containing perfluoroalkyl terminated co-oligomer concentrates and polysaccharides Co-oligmers of the formula Rf --Em --(S)n --[M1 ]x --[M2 ]y --H and mixtures thereof, wherein Rf is a perfluoroalkyl group, E is a linkage group, M1 represents a... | 06/08/1993 |
| 5217521 | Triazolylsulfonamides N-Phenyl-triazolopyrimidinyl-sulfonamides of formula I ##STR1## wherein R1 is halogen, phenyl, O-phenyl, C1 -C4 alkyl, C1 -C4 haloalkyl, --OR8, --OR9, nitro, hydroxy, cyano, ... | 06/08/1993 |
| 5217525 | Synergistic composition and method for selective weed control in rice Compositions that contain, in admixture with one another, as active ingredient, on the one hand N-[2-(2-methoxyethoxy)-phenylsulphonyl]-N'-(4,6-dimethoxy-1,3,5-triazin-2- yl)-urea of the formula ##STR1## and on the other hand one or two of the ac... | 06/08/1993 |
| 5214121 | Process for manufacturing diols and polyurethanes containing perfluoroalkyl radicals Diols containing perfluoroalkyl radicals are produced by reacting compounds of the formula Rf --(E)m --X'--H (Rf =perfluoroalkyl radical, E is an alkylene group optionally interrupted by certain groups and/or substituted at the... | 05/25/1993 |
| 5209771 | Sulfonylureas N-Phenylsulfonyl N'-triazinylureas and -thioureas of formula I ##STR1## in which X is oxygen, sulfur, SO or SO2 ; W is oxygen or sulfur; R1 is hydrogen or methyl; R2 is hydrogen, fluorine, chlorine, bromine, iodine, (... | 05/11/1993 |
| 5206395 | Photochromic naphthacenequinones, process for their preparation and the use thereof Compounds of the formula I or V, or mixtures thereof, ##STR1## wherein R is unsubstituted C6 -C14 aryl or C6 -C14 aryl which is substituted by C1 -C12 alkyl, C1 -C12 ... | 04/27/1993 |
| 5206390 | Substituted bisacyloxynaphthacenes Compounds of the formula I ##STR1## in which R1 to R8 independently of one another are H and at least one of R1 to R8 is a substituent belonging to the group --F, --Si(C1 -C4 alkyl) | 04/27/1993 |