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Combination Beverage Container and Spittoon
A combination beverage container and spittoon includes a bottom portion including outer wall and a first inner wall defining a spittoon space.
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| Number | Title | Issue Date |
| 5077413 | 1,5-Diphenyl-1,2,4-triazole-3-carboxylic acid derivatives for the protection of cultivated plants from the phytotoxic action of herbicides 1,5-Diphenyl-1,2,4-triazole-3-carboxylic acid derivatives of formula ##STR1## wherein each of Ra and Rb, independently of the other, is halogen, C1 -C5 alkyl, C1 -C5 haloalkyl, C2 | 12/31/1991 |
| 5064849 | Heterocyclic derivatives useful as radiosensitizing agents and antiviral agents A novel heterocyclic derivative of formula (I): ##STR1## wherein R1 represents ##STR2## and R2 represents hydrogen or acyl. When R2 is acyl, the derivative can be prepared, for example, by the following process: ... | 11/12/1991 |
| 5064844 | 1,2,3-triazole insecticides Compounds of formula I ##STR1## and N-oxides thereof, in which Ar is aryl; R1 and R2 are the same or different and are hydrogen, alkyl, alkenyl or alkynyl, each of which is optionally substituted, aryl, heterocyclyl, cyano, halo... | 11/12/1991 |
| 5059615 | Antimycotically active cyclopropyl-substituted azolylmethylcarbinols Antimycotically active 1-cyano- and 1-carboxamidocyclopropylazolylmethylcarbinols have now been found of the formula ##STR1## in which R1 represents hydrogen or represents alkyl or represents alkylcarbonyl, R2 represents cy... | 10/22/1991 |
| 5055586 | Desulfurization of triazolothiadiazines Pyrazolotriazoles such as 3,6-disubstituted-1H-pyrazolo[5,1-c]-1,2,4-triazoles: ##STR1## are useful in the photographic arts, e.g. as magenta couplers. They may be made from 3,6-disubstituted-7H-1,2,4-triazolo[3,4-b][1,3,4]thiadiazines: ##STR2##... | 10/08/1991 |
| 5055587 | Process for preparing 1H-pyrazolo-[5,1-c]-1,2,4-triazole compounds A process for preparing a 1H-pyrazolo[5,1-C]-1,2,4-triazole compound represented by the following general formula (I): ##STR1## wherein R1 represents a hydrogen atom or a substituent group, R2 represents an alkyl group, an aryl ... | 10/08/1991 |
| 5053504 | Process for benzazepine intermediates A process is disclosed for providing benzazepine intermediates of the formulae ##STR1## wherein R3, R4 and Y are as defined herein, which intermediates are useful in a process for the preparation of pharmaceutically useful ... | 10/01/1991 |
| 5049573 | Fungicidal substituted triazoles Fungicidal trazoles of the formula ##STR1## in which Ar stands for optionally substituted aryl, A stands for the groups ##STR2## and X stands for the groups ##STR3## wherein R1 stands for hydrogen or alkyl, R2 stands... | 09/17/1991 |
| 5049678 | 1-hydroxy-1,2,4-triazoles 1-hydroxy-1,2,4-traizoles have the general formula I ##STR1## where R1 and R2 are singly independently of the other hydrogen, alkyl, halogen or substituted or unsubstituted aryl or together an alkylene chain.... | 09/17/1991 |
| 5047549 | Derivatives of pravastatin for inhibiting cholesterol biosynthesis Derivatives of pravastatin are provided which are useful in inhibiting cholesterol biosynthesis and in preparing radiolabeled compounds useful in the radioimmunoassay (RIA) of pravastatin and derivatives thereof. The pravastatin derivatives have the struc... | 09/10/1991 |
| 5047548 | 3-aryl-3-hydroxy-4-(1H-1,2,4-triazol-1-yl)butyramide and derivatives as antifungal agents Compounds of the formula ##STR1## or a pharmaceutically or agriculturally acceptable acid addition salt thereof, wherein R is 5-chloro-2-pyridyl, or phenyl optionally substituted by one to three substituents, each independently selected from F, Cl, B... | 09/10/1991 |
| 5047415 | 2,2-dihalogenocyclopropyl-hydroxy-ethyltriazoles Novel 2,2-dihalogenocyclopropyl-hydroxy-ethyltriazoles of the formula ##STR1## in which Ar represents optionally substituted aryl, R represents alkyl, optionally substituted aryl or optionally substituted aralkyl, X1 represents halogen, X2... | 09/10/1991 |
| 5045557 | Imidazable fungicides and use thereof The invention provides compounds of formula I ##STR1## in which X, R1, R2 and R3 are as defined in the description. The compounds have valuable fungicidal activity.... | 09/03/1991 |
| 5041459 | Microbicidal hydroxy-keto-azoles Microbicidal hydroxy-keto-azoles of the formula ##STR1## in which R1 represents optionally substituted alkyl, optionally substituted alkenyl, optionally substituted cycloalkyl or optionally substituted aryl, R2 represents option... | 08/20/1991 |
| 5041651 | Asymmetrically modified boron hydride type compound and a method for producing an optically active alcohol derivative by the use thereof The present invention relates to an asymmetrically modified borohydride type compound obtained by reacting an optically active amino alcohol represented by the formula, ##STR1## or its salt with an acid with a borohydride compound; its production ... | 08/20/1991 |
| 5041551 | Process and intermediates for the preparation of triazolone derivatives Triazolone derivatives of the formula ##STR1## in which R1 and R2 each independently represents alkyl, alkenyl, alkynyl, halogenoalkyl, halogenoalkenyl, halogenoalkynyl, alkoxyalkyl, cycloalkylalkyl, cycloalkyl or represents ara... | 08/20/1991 |
| 5041458 | Fungicidal aminotriazoles and aminoimidazoles Substituted N-aminotriazoles and N-aminoimidazoles having selected substituents on the amino group and azole rings, agriculturally useful composition comprising such compounds and the use of such compounds as fungicides.... | 08/20/1991 |
| 5039815 | 1-halo-azolylethane derivatives and fungicides containing them 1-Halo-1-azolylethane derivatives of the formula I ##STR1## where R1 and R2 are C1 -C8 -alkyl, phenyl, biphenyl, naphthyl, benzyl, C3 -C8 -cycloalkyl or C3 -C8 -c... | 08/13/1991 |
| 5039816 | Process for the production of 1,2,4-triazol-5-one A process for producing chloride ion-free 1,2,4-triazol-5-one which comprises: a) heating a mixture of hydrazodicarbonamide and formic acid to a reflux temperature for said mixture, b) refluxing said mixture at said reflux temperature for a time sufficien... | 08/13/1991 |
| 5039669 | Heterocyclic bisphosphonic acid derivatives A novel heterocyclic bisphosphonic acid derivatives represented by the following general formula (I): ##STR1## in which .circle.Het means one of the following (A) and (B): ##STR2## wherein a dotted line in (A) means that two adjacent atoms ar... | 08/13/1991 |
| 5039332 | Substituted oxathiolanes This invention relates to novel imidazole and triazole substituted oxathiolane compounds and compositions containing said compounds having fungicidal and plant growth regulant activity and methods for preparing same.... | 08/13/1991 |
| 5036094 | Azolyl-derivatives endowed with antifungal activity Disclosed are compounds, having the general formula: ##STR1## wherein: m=0, 1, 2; n=0, 1 with the condition that when m=0, also n=0; p=0, 1; q=1, 2; X is either oxygen or sulphur; A=N, CH; R is H, CH3, F; R1 is selected from chlorine, bro... | 07/30/1991 |
| 5034538 | Preparation of 4-amino-1,2,4-triazol-5-ones A process for the preparation of 4-amino-1,2,4-triazol-5-one of the formula ##STR1## in which p0 R represents unsubstituted or substituted alkyl, alkenyl, cycloalkenyl, cycloalkyl, aralkyl, aryl or heterocyclyl, which comprises reacting a carbodihydrazide... | 07/23/1991 |
| 5034052 | Fungicidal and plant growth-regulating azolylmethyl-cyclopropyl derivatives Fungicidal and plant growth-regulating azolylmethylcyclopropyl derivatives of the formula ##STR1## in which R repesents halogen, alkyl or optionally substituted phenyl, or represents the groupings --Y--R2, wherein Y represents oxygen, sulp... | 07/23/1991 |
| 5028598 | Oxetanocin derivatives and their salts as well as use thereof Oxetanocin derivatives represented by formula: ##STR1## wherein X represents H or ##STR2## or a pharmacologically acceptable salt thereof exhibit an anti-viral activity. Anti-viral compositions comprising the oxetanocin derivatives or their... | 07/02/1991 |
| 5028716 | 3,5-diamino-1,2,4-triazole derivatives A triazole derivative represented by the formula ##STR1## wherein R1 is a hydrogen atom, a lower alkyl group having 1 to 4 carbon atoms, an acetyl group, a naphthylmethyl group, an anthrylmethyl group or a group of the formula ##STR2#... | 07/02/1991 |
| 5028254 | Azole derivatives and agricultural and horticultural chemical composition containing the same Disclosed herein are an azole derivative represented by the formula (I): ##STR1## wherein R1 and R2 respectively represent a (C1 -C5) alkyl group or a hydrogen atom; X represents a halogen atom, a (C1... | 07/02/1991 |
| 5026720 | 1-hydroxyazole compounds and fungicides containing these Compounds of the general formula I ##STR1## where X is alkyl, aryl, aryloxy or alkoxy, Y is hydrogen, alkyl, alkoxy, halogen, aryl or aryloxy, n is 0 to 5, and Z is CH or N, and fungicides containing these compounds.... | 06/25/1991 |
| 5026718 | Triazole alkanols including an alkenyl substituent having fungicidal and plant growth regulating properties Compunds of formula: ##STR1## and stereo isomers thereof, wherein R is optionally substituted phenyl, alkyl or cycloalkyl and R1 and R2 are hydrogen or alkyl, alkenyl or alkynyl groups; Z is a straight or branched chain aliphati... | 06/25/1991 |
| 5025030 | Hydroxyalkinyl-azolyl derivatives Novel hydroxyalkinyl-azolyl derivatives of the formula ##STR1## in which Ar represents optionally substituted aryl, R represents alkyl, optionally substituted aryl or optionally substituted aralkyl, X1 represents halogen, X2 represen... | 06/18/1991 |
| 5021442 | Fungicide azolyl-derivatives There are described compounds having general formula: ##STR1## wherein: R1 is selected from the group comprising F, Cl, Br, CF3, a phenyl, a C1 -C2 alkoxy, a C1 -C2 haloalkoxy, an alky... | 06/04/1991 |
| 5021082 | Herbicidal substituted sulphonylaminoazoles Herbicidal substituted sulphonylaminoazoles of the formula ##STR1## in which R1 is optionally substituted alkyl, aralkyl, aryl or heteroaryl, R2 is hydrogen or --SO2 --R1, R3 is hydrogen, halogen, hyd... | 06/04/1991 |
| 5021081 | Herbicidal substituted triazoles Herbicidal substituted triazoles of the formula ##STR1## in which R1 and R2 independently of one another each stands for hydrogen, alkyl, alkenyl, alkinyl, halogenoalkyl, halogenoalkenyl, halogenoalkinyl, alkoxyalkyl, cycloalkyl... | 06/04/1991 |
| 5021080 | Herbicidal substituted 4-amino-5-alkylthio-1,2,4-triazol-3-ones Herbicidal substituted 4-amino-5-alkylthio-1,2,4-triazol-3-ones of the formula ##STR1## in which R1 represents in each case straight-chain or branched alkyl, alkenyl or alkinyl, each of which has up to 4 carbon atoms, and R2 rep... | 06/04/1991 |
| 5017595 | Azolylmethylallyl alcohols and fungicides containing these compounds Azolylmethylallyl alcohols of the formula I ##STR1## where R1 and R2 are alkyl, naphthyl, biphenyl, cycloalkyl, cycloalkenyl or phenyl, these radicals being unsubstituted or substituted, X is CH or N, their plant-tolerated acid ... | 05/21/1991 |
| 5017594 | 1-halo-1-azolylpropenes and -methyloxiranes and fungicides containing these compounds 1-Halo-1-azolylpropenes and -methyloxiranes of the formula I ##STR1## where R1 and R2 are alkyl, cycloalkyl, cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl, A is oxygen or a single bond, R... | 05/21/1991 |
| 5015651 | Treatment of hypertension with 1,2,4-angiotensin II antagonists Substituted pyrroles, pyrazoles and traizoles such as ##STR1## and their pharmaceutically suitable salts are useful as antihypertensive agents and for treatment of congestive heart failure.... | 05/14/1991 |
| 5011934 | Process for preparing 1-alkylimidazoles Imidazoles are alkylated at the 1-position by adding an alkyl halide a mixture comprising an imidazole, a non-reactive aromatic solvent and a base at temperature of from about 75° C. to about 115° C. and then maintaining the temperature for a period of ... | 04/30/1991 |
| 5011933 | Nitration of phenyl triazolinones Process for the nitration of a compound of formula I below with nitric acid in sulfuric acid, according to the following general equation: ##STR1## where X is a Cl or F and R is haloalkyl, for example CHF2 or CF2 CHF2... | 04/30/1991 |
| 5011850 | Substituted diazolylalkyl-carbinols, a process for their preparation and their use as antimycotic agents The invention relates to compounds and their derivatives, said compounds being described herein as those of Formula (I). The compounds and compositions containing them are effective antimycotic agents and the invention includes methods for the use of said... | 04/30/1991 |
