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Method and apparatus for making a drink hop along a bar or counter
A method for generating a drink which appears to hop from a remote spot on the bar or counter and take one or more leaps, before landing in a patron's glass.
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| Number | Title | Issue Date |
| 7999118 | Process for producing N-halogenated hydantoins This invention provides a process for the N-halogenation of at least one 5-hydrocarbyl hydantoin and/or at least one 5,5-dihydrocarbyl hydantoin. The process comprises concurrently feeding into a reaction zone (i) water, inorganic base, and 5,5-dimethylhydantoin, th... | 08/16/2011 |
| 7897785 | 1,3-Diiodohydantoin compound and production method thereof The present invention provides a means which can inhibit release of I2 in production or storage of 1,3-diiodohydantoin compound, and thereby solve decrease in purity of the compound and various problems caused by I2. The present inventio... | 03/01/2011 |
| 7207732 | Coated optical fiber and curable compositions suitable for coating optical fiber The present invention provides materials suitable for use as secondary coatings of optical fibers or the re-coating of spliced optical fiber junctions. With regard to the latter use, the coating materials a preferably characterized by a Young's modulus that is at le... | 04/24/2007 |
| 6965035 | Compacted forms of halogenated hydantoins This invention provides a method of producing granules. This method comprises roll compaction of a 1,3-dihalo-5,5-dimethylhydantoin/binder blend, followed by feeding the compacted product obtained from the roll compactor into a mechanical device, where the compacted... | 11/15/2005 |
| 6809205 | Process for producing N-halogenated organic compounds The process enables highly effective N-halogenation of a compound having one or more halogenatable amido or imido functional groups in the molecule. The process involves, for example, concurrently feeding into a reactor (i) water, inorganic base, and the compound to... | 10/26/2004 |
| 6683190 | Method for preparing chiral amino acids The invention concerns a novel method for preparing chiral amino acids of formula (I) characterised in that it consists in contracting a racemic hydantoin of formula (II) with an enantiomeric splitting agent. ##STR1##... | 01/27/2004 |
| 6495698 | Binder-free compacted forms of 1,3-dihalo-5,5-dimethylhydantoins Novel, binder-free compacted forms of 1,3-dihalo-5,5-dimethylhydantoins in which one halogen atom is chlorine and the other is a bromine or chlorine atom are produced and used for microbiological control in aqueous media and water.... | 12/17/2002 |
| 6448410 | Production of compacted biocidal agent from particulate biocidal agent without using a binder A shape-retentive compacted article is produced from 1,3-dibromo-5,5-dimethylhydantoin particulate solids by (a) granulating the particulate solids without use of a binder, and (b) pressure compacting granulated 1,3-dibromo-5,5-dimethylhydantoin granules ... | 09/10/2002 |
| 6429181 | Partially halogenated hydantoins in papermaking applications The inventors have discovered that partially halogenated hydantoins exhibit superior antimicrobial efficacy and decreased performance additive decomposition rates than fully halogenated hydantoins, such as dichlorodimethyl hydantoin (DCDMH). Partially hal... | 08/06/2002 |
| 6353013 | Small molecules useful in the treatment of inflammatory disease Novel compounds of the formula I ##STR1## which are useful for treating or preventing inflammatory and immune cell-mediated diseases. Exemplary compounds are: 5-(R)-(4-bromobenzyl)-3-(3-chloro-5-nitrophenyl)-5-methylimidazoline-2,4-di one; and, 5-(R)-(4-br... | 03/05/2002 |
| 6335451 | Five-membered heterocycles having biphenylsulfonyl substitution, with sulfonylcyanamide side chain, compositions containing them, and methods of using them Five-membered heterocycles having biphenylsulfonyl substitution, process for their preparation, their use as a medicament or diagnostic, and medicament comprising them. Compounds of the formula I ##STR1## in which the symbols have the meanings indicated i... | 01/01/2002 |
| 6127583 | Process for preparing acetylene derivative from a ketone compound A preparation process of an acetylene derivative comprising reacting a compound having a skeleton represented by the formula (1): ##STR1## in the molecular formula with a compound represented by the formula (2): ##STR2## wherein R1, R... | 10/03/2000 |
| 6107488 | Phenylimidazolidine preparation process A subject of the invention is a preparation process for the products of formula (I): ##STR1## in which R1 and R2 represent in particular hydrogen, cyano, halogen or amino,R3 represents in particular hydrogen or hydrox... | 08/22/2000 |
| 6087509 | 1-Imidazolidinyl-phenyls A particular subject of the invention is the products of formula (I): ##STR1## in which: R1 and R2 represent in particular cyano and trifluoromethyl, R3 represents in particular alkyl, alkenyl or alkynyl, optionally s... | 07/11/2000 |
| 6054591 | Lymph-absorbable aryl substituted imidazole derivatives A compound of the formula (I): ##STR1## salt thereof, or hydrate thereof which can effectively be absorbed from the lymph vessel in the intestinal tract and transferred to the lymph node in a high concentration is provided.... | 04/25/2000 |
| 5877324 | 2-(substituted sulfanyl)-3,5-dihydro-imidazol-4-one derivatives The compound of formula I: ##STR1## wherein R is phenyl or phenyl optionally substituted with one or more groups selected from halogen, alkyl, perfluoroalkyl, alkoxy, perfluoroalkoxy, hydroxy, alkanoyloxy, aroyloxy or arylalkanoyloxy; R3 | 03/02/1999 |
| 5817685 | Anticonvulsive imidazoline-2,4-diones and process for making Anticonvulsive compounds and compositions, of the formula ##STR1## in which X is a C1-4 -alkyl, trifluoromethyl, or halogen residue, Y is hydrogen or halogen, n is 0 or 1, and m is 0 or a cardinal number from 1 to 4, and its pharmacologica... | 10/06/1998 |
| 5783707 | 2-thioxo-imidazolidin-4-one derivatives The compound of formula I ##STR1## in which R1 is alkyl; and R is alkyl, naphthyl, benzhydryl, fluorophenylmethyl, phenethyl, 1-(fluorophenyl)ethyl, 5-chloro-2-methoxyphenyl, trifluoromethoxyphenyl, trifluoromethylphenyl, methylsulfan... | 07/21/1998 |
| 5780641 | Stabilization of halogenated dialkyl hydantoins Method for stabilizing halogenated hydrantoins, comprising mixing the hydantoin with dry calcium hydroxide.... | 07/14/1998 |
| 5663363 | 2-thioxo-imidazolidin-4-one derivatives The compound of formula I ##STR1## in which R is alkynyl; and X and Y are, independently, alkyl, halo, perfluoralkyl, perfluoralkoxy, or, taken together, X and Y are ortho substituted trimethylene or tetramethylene are useful for increasing blood ... | 09/02/1997 |
| 5627201 | Phenylimidazolidines having antiandrogenic activity A compound of the formula ##STR1## wherein R1 is selected from the group consisting of --CN, --NO2 and halogen, R2 is --CF3 or halogen, --A--B-- is selected from the group consisting of ##STR2## X... | 05/06/1997 |
| 5606071 | Process for preparing 5-arylhydantoins using 5-hydantoin, a halogenating agent and p-phenol The present invention provides a novel process for the preparation of 5-arylhydantoins as an important intermediate of (D)-arylglycines (e.g., (D)-p-hydroxyphenyl-glycine) useful for the synthesis of semisynthetic penicillines and cephalosporins, the proc... | 02/25/1997 |
| 5589497 | Phenylimidazolidines A compound selected from the group consisting of compounds of the formula ##STR1## wherein R1 and R2 are individually selected from the group consisting of --CN, --NO2, halogen, --CF3, free carboxy, salifie... | 12/31/1996 |
| 5565575 | Method for the production of 5-cyclohexylmethylhydantoin derivatives 5-Cyclohexylmethylhydantoin derivatives may be conveniently prepared by reducing, in the presence of a metal catalyst, a 5-(3-cyclohexene-1-yl)melthylenehydantoin derivative which is obtained by the condensation of a hydantoin derivative and a 3-cycl... | 10/15/1996 |
| 5411981 | Phenylimidazolidines having antiandrogenic activity A compound of the formula ##STR1## wherein R1 is --CN, --NO2 or halogen, R2 is --CF3 or halogen, --A-B-- is of ##STR2## X is --O-- or --S--, R3 is hydrogen, alkyl, alkenyl or alkynyl of up ... | 05/02/1995 |
| 5358946 | Heterocycle-substituted amides, carbamates and ureas as agents for the treatment of atherosclerosis This invention relates to imidazoles, namely, heterocycle-substituted amides, carbamates and ureas as inhibitors of acyl-CoA: cholesterol acyltransferase (ACAT), pharmaceutical compositions containing them, and their use as antihypercholesterolemic and/or... | 10/25/1994 |
| 5346913 | N-iodopropargyl hydantoin compounds, compositions, preparation, and use as antimicrobial agents N-Iodopropargyl hydantoin compounds, methods of preparing, compositions comprising, and methods of use as antimicrobials and antifungal agents in a variety of applications.... | 09/13/1994 |
| 5326780 | Imidazole derivatives having anti-HIV activity A novel imidazole derivatives of formula I: ##STR1## wherein R1 is hydrogen, alkyl, halogen, or optionally substituted aryl; R2 is alkyl, optionally substituted aryl optionally substituted aralkyl, or optionally substituted hete... | 07/05/1994 |
| 5326878 | Method for the resolution of chiral hydantoins Method of resolution of chiral hydantoins of the general formula I ##STR1## in which: R1 designates a lower alkyl radical comprising 1 to 5 carbon atoms in linear or branched chain, R2 designates a phenyl radical, possibly mono-, di-... | 07/05/1994 |
| 5223525 | Pesticidal 1-arylimidazoles The invention describes novel 1-arylimidazoles of formula (I) ##STR1## wherein typically preferred substituents are: X is S(O)n R1, in which R1 is an alkyl group, preferably a methyl group, which is fully substituted ... | 06/29/1993 |
| 5214064 | Phenoxyphenylmethyl substituted azoles and pesticidal composition thereof N-substituted azoles of the formula I ##STR1## where R1, R2, R3 are each hydrogen, halogen, C1 -C8 -alkyl, C1 -C8 -alkoxy, C1 -C4 -haloalkyl, C1 | 05/25/1993 |
| 5177097 | Acyl amidine and acyl, guanidine substituted biphenyl derivatives Novel compounds are disclosed having the formula ##STR1## and wherein R1, R2 and R3 are as defined herein. These compounds inhibit the action of angiotensin II and are useful, therefore, for example, as antihypertensi... | 01/05/1993 |
| 5087634 | N-substituted imidazol-2-one compounds for treatment of circulatory disorders A class of N-substituted imidazol-2-one compounds is described for use in treatment of circulatory disorders. Compounds of particular interest are angiotensin II antagonists of the formula ##STR1## wherein m is one; wherein R1 is selected ... | 02/11/1992 |
| 4792556 | Naphthalene anti-psoriatic agents Psoriasis in mammals is relieved by topically administering naphthalenes of the formula: ##STR1## wherein: R1 and R2 are the same and are lower alkoxy or optionally substituted phenoxy, R3 is lower alkyl, lower alkoxy... | 12/20/1988 |
| 4745189 | Method of preparing N-halogenated organic heterocyclic compounds A method of preparing N-halogenated organic heterocyclic compounds by reacting in an aqueous mixture under alkaline conditions (e.g. NaOH) and in the presence of a halogenated organic compound (e.g. methylene chloride), a N-hydrogen organic heterocyclic c... | 05/17/1988 |
| 4698165 | Shock treatment of aqueous systems A process for controlling the formation of undesirable by-products in an aqueous system containing residual halogenated 5,5-dialkyl hydantoins is disclosed. The process comprises the steps of treating the aqueous system with bromide ion and shocking the a... | 10/06/1987 |
| 4681948 | N,N'dihalo-2-imidazolidinones N-chloro and N-bromo derivatives of 2-imidazolidinones having substituents at the 4 and 5 positions of the ring are described. More particularly, there are described dichloro, dibromo-, and chlorobromo-derivatives of 2-imidazolidinones having at least thr... | 07/21/1987 |
| 4677130 | Process of densification of N-halohydantoin compositions and products thereof The present invention is directed to a novel process for manufacturing tablets of N-halohydantoin compounds. In the process, at least one dry, particulate N-halohydantoin compound is blended with a dry, particulate alkali metal or alkaline earth salt to f... | 06/30/1987 |
| 4654424 | Method for preparing halogenated hydantoins A halogenated hydantoin product and method of producing same for use as e.g. a bleaching agent or disinfectant comprising a halogenated hydantoin of the formula ##STR1## wherein R is methyl or ethyl and X1 and X2 which may be th... | 03/31/1987 |
| 4650876 | Hydrogenation of substituted, unsaturated hydantoins to substituted, saturated hydantoins Unsaturated hydantoins are reduced to the corresponding saturated hydantoin by carrying out the hydrogenation reaction using a nickel catalyst in the presence of more than a stoichiometric amount of caustic. Use of this process allows for almost complete ... | 03/17/1987 |
