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 |
| 3974157 | 1-(Amino-alkyl)-2-aryl-cyclohexane alcohols and esters Analgesics, local anesthetics, and antiarrhythmics which are 1-(amino-alkyl)-2-aryl-cyclohexane alcohols and esters having the structure ##SPC1## Wherein R1 is hydrogen or alkanoyl; R2 and R3 individually are hydrogen... | 08/10/1976 |
| 3974158 | 2-(Substituted anilino)methylmorpholines The disclosure relates to new 2-(substituted anilino)methylmorpholine derivatives which possess antidepressant activity, to processes for the manufacture of the said morpholine derivatives and to pharmaceutical compositions containing them. Typical of the... | 08/10/1976 |
| 3974159 | Manufacture of derivatives of malondialdehyde Compounds of the general formula ##EQU1## which may be used in place of malondialdehyde in synthesis reactions are obtained in a one-step reaction form dimethylformamide, phosgene and an alkyl vinyl ether.... | 08/10/1976 |
| 3974160 | Water-insoluble reactive dyestuffs which are soluble in aprotic solvents Valuable reactive dyestuffs containing no acid, salt-forming, water-solubilizing groups and which, among others, can be applied from organic solvents, especially aprotic solvents correspond to the formula ##EQU1## wherein D represents the radical of ... | 08/10/1976 |
| 3974161 | Fused pyrimidin-4(3H)-ones as antiallergy agents Fused heterocyclic ring systems in which a quinoline or a pyridine component is "fused" to a pyrimidine having a 2-methyl, 2-ethyl, or 2-acetyl group and a 4-keto group, and to similar ring systems in which a quinoline, a naphthalene or a pyridine compone... | 08/10/1976 |
| 3974162 | 4-Pyrimidinylthioacetic acid derivatives The compounds ##SPC1## In which the symbol A represents a carbon or nitrogen atom, X represents --Cl, lower alkoxy or the substituted amino group ##SPC2## Y represents --Cl, lower alkoxy, ##SPC3## With the proviso that when Y is --Cl, X and Z are oth... | 08/10/1976 |
| 3974163 | Poly(thiomaides) New compounds with a nucleus of ##EQU1## WHERE N IS 2 TO 4 AND ##EQU2## is a radical derived by removal of hydrogen from an imide of an acyclic dicarboxylic acid, from a monocarbonyl cyclic urea, from an imide in which nitrogen is linked to... | 08/10/1976 |
| 3974164 | Reserpic acid derivatives The invention relates to compounds having the formula: ##SPC1## In which R is a group --NHR1, --NH--COOR2, --NH--CO--R3, -CONH--Ar, --NH--CS--NH--Ar or --N=CH--Ar, R1 being hydrogen, R2 being lower alkyl ... | 08/10/1976 |
| 3974165 | Hypotensive agents Optionally substituted 1-H-2,3,3a,4-Tetrahydro-2-oxopyrrolo[2,3-b]quinolines or the pharmaceutically acceptable salts thereof are compounds useful as blood platelet anti-aggregative and/or antihypertensive agents in mammals, including humans.... | 08/10/1976 |
| 3974166 | Process for the manufacture of bromopyridines A novel process for the preparation of 2,4-dibromo-, 2,6-dibromo- and 2,4,6-tribromopyridines, and the new bromopyridines to be obtained therewith, are disclosed. The novel process comprises treating 2,4-dichloro-, 2,6-dichloro- and 2,4,6-trichloropyridin... | 08/10/1976 |
| 3974167 | (7-Nitro-2-aza-9-fluorenylidene) malononitrile Photosensitive material for use in electrophotography which is a charge transfer complex comprising (mononitro-2-aza-9-fluorenylidene) malononitrile and an organic photoconductor.... | 08/10/1976 |
| 3974168 | Tricycle substituted acetones Compounds of the formula: ##SPC1## Wherein Of X1 and X2 is a hydrogen atom, a halogen atom or an alkyl group having 1 to 4 carbon atoms; R1 is a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, an alkenyl group ha... | 08/10/1976 |
| 3974169 | -[2-(2-Pyridyl)ethylamino]phenylacetic acid dihydrochloride Hemihydrate A compound -[2-(2-Pyridyl)ethylamino]phenylacetic acid dihydrochloride Hemihydrate possesses pharmacological activity as an antihypertensive agent.... | 08/10/1976 |
| 3974170 | Preparation of 2-mercaptoazoles A process is disclosed which comprises reacting hydrogen sulfide with azolesulfonates and sulfinates to give 2-mercaptoazoles. One embodiment of the invention describes removal of oxidized forms of 2-mercaptobenzothiazole including benzothiazole-2-sulfona... | 08/10/1976 |
| 3974171 | O-[3-methyl-1,3,4-triazol e-(2,3,-b)-thiazol(6)yl]-(thiono)-phosphoric(phosphonic) acid esters O-[3-methyl-1,2,4-triazole-(2,3-b)-thiazol(6)yl]-(thiono)-phosphoric(phosph onic) acid esters of the formula ##EQU1## in which R is alkyl with 1 to 6 carbon atoms, R' is alkyl with 1 to 4 carbon atoms, alkoxy with 1 to 6 carbon atoms or phenyl, R" is ... | 08/10/1976 |
| 3974172 | Benzofuran derivatives Benzofuran compounds of the formula ##SPC1## Wherein E is a bivalent bridging member of the formula ##SPC2## S is hydrogen, halogen, lower alkyl, carboxy, sulfo, cyano, lower carboalkoxy, carbonamido, lower mono- or dialkyl carbonamido, sulfonic acid... | 08/10/1976 |
| 3974173 | Oxazolidines of endo-6-formyl-exo-3-hydroxybicyclo[3.1.0]hexan-exo-2-acetic acid, δ- l Oxazolidines having the formula ##SPC1## Wherein ~ indicates endo or exo attachment, but differing in their stereoisomeric configuration, are prepared by reaction of the isomers of a tricyclic lactone aldehyde of the formula ##SPC2## Wherein ~ is as ... | 08/10/1976 |
| 3974174 | 1-(1,2,4-Triazolyl-1')-2-phenoxy-4,4-dimethyl-pentan-3-ones 1-(1,2,4-TRIAZOLYL-1')-2-PHENOXY-4,4-DIMETHYL-PENTAN-3-ONES OF THE FORMULA ##SPC1## In which n is an integer from 0 to 5, X is halogen, halogenoalkyl, alkyl, alkoxy, alkylthio, alkylsulfonyl, nitro, nitrile, carbalkoxy or phenyl, and Y is a keto group or a fun... | 08/10/1976 |
| 3974175 | Nitro-chromeno pyrazole compounds their manufacture and use Nitro-chromenopyrazole compounds of the formula ##SPC1## Wherein R1 and R2, independently of the other, represent hydrogen, alkyl with 1 to 12 carbon atoms, alkoxyalkyl with 2 to 8 carbon atoms, cycloalkyl with 5 or 6 carbon atoms, b... | 08/10/1976 |
| 3974176 | Halogen pyrazoles derivatives, a method for producing these halogen pyrazole derivatives and medicaments containing them 1,3-Diaryl-5-halogen-pyrazole-4-acetic acids and their derivatives with analgetic, antipyretic and antiphlogistic action are described.... | 08/10/1976 |
| 3974177 | Process for the purification of crude polyhalo copper phthalocyanines Polyhalo copper phthalocyanines are purified in concentrated sulfuric acid under addition of peroxo compounds including addition compounds of hydrogen peroxide. The products are useful as pigments having very pure green shades and good fastness properties... | 08/10/1976 |
| 3974178 | Naphthostyril cationic dyes A compound of the formula (I): ##SPC1## wherein R1 is a C1 -C4 alkyl or C1 -C2 alkoxy- or cyano-substituted C1 -C4 alkyl, R2 is a C1 -C4 alkyl, phenyl... | 08/10/1976 |
| 3974179 | 1,3,4,9-Tetrahydropyrano[3,4-b]indole-1-acetamides and derivatives Indole derivatives characterized by having a 1,3,4,9-tetrahydropyrano[3,4-b]indole or 1,3,4,9-tetrahydrothiopyrano[3,4-b]indole nucleus bearing a substituent in position 1, said substituent incorporating an acid, ester or amide function therein, are ... | 08/10/1976 |
| 3974180 | Furanes, their manufacture and use The invention relates to specific naphthofuranes which are useful as cryochromic substances e.g. for measuring the temperature, pH value or radiation field.... | 08/10/1976 |
| 3974181 | Trimethyl-1,4-dioxaspiro[4,5]dec-7-en-8-methanol The compound 7,9,9-trimethyl-1,4-dioxoaspiro [4,5] dec-7-en-8-methanol an intermediate in the preparation of Zeaxanthin and Xanthophyll, known coloring agents for foodstuffs.... | 08/10/1976 |
| 3974182 | Intermediates for the preparation of trienic steroids Novel intermediates for the preparation of trienic steroids which intermediates have the formula ##SPC1## Wherein R is alkyl of 1 to 4 carbon atoms and X is selected from the group consisting of aliphatic of 1 to 6 carbon atoms optionally substituted and ... | 08/10/1976 |
| 3974183 | Reduction of trans-1-(2-carboxymethyl-3-hydroxy-5-p-phenylbenzoyloxycyclopentyl)-1-oc ten-3-one-γ-lactone A process for reducing trans-1-(2-carboxymethyl-3-hydroxy-5-acyloxycyclopentyl)-1-octen-3-one-.ga mma.-lactone to the corresponding 3-ol which makes use of trihydrocarbylborohydride reagents, some of which are new, e.g. lithium 2-thexyl-8-methyl-2-bor... | 08/10/1976 |
| 3974184 | Microbial production of certain isoflavones This invention relates to the novel compounds 3',5,7-trihydroxy-4',6-dimethoxy-isoflavone, 3'5,7-trihydroxy-4',8-dimethoxy-isoflavone and 3',7-dihydroxy-4',6,8-trimethoxy-isoflavone which are powerful inhibitors of catechol-O-methyl transferase (COMT... | 08/10/1976 |
| 3974185 | Hexahydro-cyclopentano[b]furans having a 2-C.tbd.C containing substituent in the 4-position Process for synthesizing a prostaglandin from a hexahydro-4-(lower alkoxy)-2H-oxireno[3,4]cyclopenta[1,2-b]furan, utilizing as an intermediate in the process a hexahydro-5-hydroxy-2-lower alkoxy-2H-cyclopenta[b]furan-4-carboxyaldehyde, and the novel ... | 08/10/1976 |
| 3974186 | Bis-basic ethers of 2,6- and 2,7-dihydroxyanthraquinones Disclosed are novel compounds and pharmaceutical formulations having antiviral activity. The disclosed compounds have the formula ##SPC1## Wherein one R2 is a hydrogen atom and the other R2 is the radical ##SPC2## A is a straight cha... | 08/10/1976 |
| 3974187 | Synthetic analogs having the activity of naturally occurring forms of coenzyme Q Synthetic 2,3-dimethoxy-5-methyl-1,4-benzoquinone is converted into a series of new 6-alkyl derivatives. These 6-alkyl derivatives have straight carbon chains which are both saturated and unsaturated. The unsaturated derivatives contain one, two, three an... | 08/10/1976 |
| 3974188 | Process for producing cholestane type steroids A process for producing cholestanyl phosphate or epicholestanyl phosphate or salts thereof in which the hydroxyl group at the three-position of cholestanol or epicholestanol is converted into the phosphoric ester by reaction with a phosphorylating agent i... | 08/10/1976 |
| 3974189 | 16-Fluoro prostaglandin E2 analogs Prostaglandin-type compounds with one or two fluoro substituents at the C-16 position are disclosed, with processes for making them. These compounds are useful for a variety of pharmacological purposes, including anti-ulcer, inhibition of platelet aggrega... | 08/10/1976 |
| 3974190 | 16-Fluoro prostaglandin A1 analogs Prostaglandin-type compounds with one or two fluoro substituents at the C-16 position are disclosed, with processes for making them. These compounds are useful for a variety of pharmacological purposes, including anti-ulcer, inhibition of platelet aggrega... | 08/10/1976 |
| 3974191 | 16-Fluoro prostaglandin F1 analogs Prostaglandin-type compounds with one or two fluoro substituents at the C-16 position are disclosed, with processes for making them. These compounds are useful for a variety of pharmacological purposes, including anti-ulcer, inhibition of platelet aggrega... | 08/10/1976 |
| 3974192 | 16-Fluoro prostaglandin B1 analogs Prostaglandin-type compounds with one or two fluoro substituents at the C-16 position are disclosed, with processes for making them. These compounds are useful for a variety of pharmacological purposes, including anti-ulcer, inhibition of platelet aggrega... | 08/10/1976 |
| 3974193 | 16-Fluoro prostaglandin B2 analogs Prostaglandin-type compounds with one or two fluoro substituents at the C-16 position are disclosed, with processes for making them. These compounds are useful for a variety of pharmacological purposes, including anti-ulcer, inhibition of platelet aggrega... | 08/10/1976 |
| 3974194 | Method of separating cobalt catalyst from a liquid polyol ester product In the method of manufacturing liquid polyol esters of carboxylic acid by making an olefin having 3 or more carbon atoms, carbon monoxide and polyhydric alcohol react with one another in the presence of a cobalt compound catalyst, the steps comprising hea... | 08/10/1976 |
| 3974195 | 2A,2B-Dihomo-15-alkyl-PGF2.sub. analogs 2a,2b-Dihomo-15-methyl and 15-ethyl PGF- and PGE-type compounds are disclosed with processes for making them. These compounds are useful for a variety of pharmacological purposes, including anti-ulcer, inhibition of platelet aggregation, increase of nasal... | 08/10/1976 |
| 3974196 | Method for disproportionating ethylenically unsaturated compounds having functional ester groups A method for the conversion of an unsaturated compound having a functional group, characterized by contacting [1] at least one compound selected from the group consisting of carboxylic acid esters, nitriles, ketones, amides, and ethers and having a carbon... | 08/10/1976 |