| Class / Patent application number | Description | Number of patent applications / Date published |
|---|
| 568382000 |
Acyclic
| 109 |
| 568338000 |
Processes of preparing, purifying, or recovering alicyclic ring containing ketones
| 102 |
| 568308000 |
Benzene ring containing
| 88 |
| 568376000 |
Six-membered alicyclic ring containing
| 25 |
| 568367000 |
Plural alicyclic rings containing
| 11 |
| 568375000 |
Containing alicyclic ring having at least seven members | 2 |
| 20110313201 | OPTICALLY ACTIVE MUSCONE COMPOSITION AND FRAGRANCES OR COSMETICS CONTAINING THE SAME - (Problem) The object of the invention relates to a development of a new musk-feeling fragrance material which is a highly scenting musk-feeling fragrance, and is to provide a fragrance composition which, when added to fragrances or cosmetics, can improve the fixative property and express a high performance and excellent musky aromatic quality. | 12-22-2011 |
| 20140323768 | 3-METHYL-6-CYCLOHEXADECEN-1-ONE AND ITS USE IN PERFUME COMPOSITIONS - The present invention is directed to a novel fragrance compound, 3-methyl-cyclohexadec-6-enone. | 10-30-2014 |
| 568305000 |
Nitrogen containing | 2 |
| 20100094060 | NITROXYL ION SOURCE WITH SECOND ORDER REACTION NITROXYL RELEASE - C-nitroso compound releases nitroxyl ion in blood in a second order reaction. | 04-15-2010 |
| 20160250625 | METHOD OF PRODUCING OPTICALLY ACTIVE COMPOUND | 09-01-2016 |
| 568379000 |
Five-membered alicyclic ring containing | 1 |
| 20100179352 | PROCESS FOR THE PREPARATION OF CYCLOPENTANONE - The invention relates to a method for producing cyclopentanone. Said method comprises the step of reacting a mixture (G1), which contains at least cyclopentene, with a mixture (G2), which contains at least dinitrogen monoxide. The reaction is carried out in at least one reactor (R1) having channels with a diameter in the range of 0.1 mm to 50 mm, the reactor comprising at least two zones (Z1) and (Z2) having channels with different diameters and the diameters of the channels of zone (Z1) being smaller than the diameter of the channels of zone (Z2). | 07-15-2010 |
| 568304000 |
With preservative or stabilizer | 1 |
| 20080221365 | PROCESS FOR STABILIZING CYCLOBUTANONE DERIVATIVES - A process for stabilizing cyclobutanone derivatives, comprising adding at least one of an alkali metal carbonate, alkali metal oxide, alkaline earth metal carbonate, and alkaline earth metal oxide as a stabilizer to at least one cyclobutanone derivative of the structure | 09-11-2008 |
| Entries |
| Document | Title | Date |
|---|
| 20080255392 | PROCESS FOR PRODUCING CYCLOALKANOL AND/OR CYCLOALKANONE - There is provided a process with which the cycloalkane is oxidized so as to produce a cycloalkanol and/or a cycloalkanone with an improved conversion of the cycloalkane. | 10-16-2008 |
| 20080306306 | Method for Producing 2-Adamantanol and 2-Adamantanone - The present invention is a process for producing 2-adamantanol and 2-adamantanone from 1-adamantanol, by using as a catalyst a substance comprising at least one kind of acid catalyst selected from Lewis acid(s) and solid acid(s) that coexist with at least one kind selected from the group consisting of carboxylic acids, sulfonic acids, and phosphoric acids, and provides a process suitable for mass production of 2-adamantanol and 2-adamantanone selectively with high efficiency without using sulfuric acid as a catalyst, thereby enabling laborsaving in waste acid treatment step and drastic reduction of the reaction time. | 12-11-2008 |
| 20110190543 | Oxidation of Alkylaromatic Compounds - In a process for oxidizing an alkylaromatic compound to the corresponding hydroperoxide, a feed comprising an alkylaromatic compound is contacted with an oxygen-containing gas in the presence of a catalyst comprising a cyclic imide. The contacting is conducted at a temperature of about 90° C. to about 150° C., with the cyclic imide being present in an amount between about 0.05 wt % and about 5 wt % of the alkylaromatic compound in the feed and the catalyst being substantially free of alkali metal compounds. The contacting oxidizes at least part of the alkylaromatic compound in said feed to the corresponding hydroperoxide. | 08-04-2011 |
| 20110245542 | SYNTHESIS OF LIQUID FUELS AND CHEMICALS FROM OXYGENATED HYDROCARBONS - Processes and reactor systems are provided for the conversion of oxygenated hydrocarbons to hydrocarbons, ketones and alcohols useful as liquid fuels, such as gasoline, jet fuel or diesel fuel, and industrial chemicals. The process involves the conversion of mono-oxygenated hydrocarbons, such as alcohols, ketones, aldehydes, furans, carboxylic acids, diols, triols, and/or other polyols, to C | 10-06-2011 |
| 20110245543 | SYNTHESIS OF LIQUID FUELS AND CHEMICALS FROM OXYGENATED HYDROCARBONS - Processes and reactor systems are provided for the conversion of oxygenated hydrocarbons to hydrocarbons, ketones and alcohols useful as liquid fuels, such as gasoline, jet fuel or diesel fuel, and industrial chemicals. The process involves the conversion of mono-oxygenated hydrocarbons, such as alcohols, ketones, aldehydes, furans, carboxylic acids, diols, triols, and/or other polyols, to C | 10-06-2011 |
| 20130172624 | PROCESS FOR THE OXIDATION OF ALKYLAROMATIC HYDROCARBONS CATALYZED BY N-HYDROXY DERIVATIVES - Process for the oxidation of alkylaromatic hydrocarbons to hydroperoxide catalyzed by N-hydroxy derivatives in the presence of a solvent which includes recovering the catalyst from the oxidation mixture by the possible removal of the solvent by distillation and/or cooling of the oxidation mixture, with the consequent precipitation and filtration of the N-hydroxy-derivative catalyst, and adsorption with non-basic adsorbing solids for the substantially complete recovery of the catalyst. | 07-04-2013 |
