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Additional ring containing

Subclass of:

568 - Organic compounds -- part of the class 532-570 series

568000000 - ORGANIC COMPOUNDS (CLASS 532, SUBCLASS 1)

568300000 - OXYGEN CONTAINING (E.G., PERCHLORYLBENZENE, ETC.)

568700000 - Hydroxy containing (H of -OH may be replaced by a Group IA or IIA light metal)

568715000 - Benzene ring containing

Patent class list (only not empty are listed)

Deeper subclasses:

Class / Patent application numberDescriptionNumber of patent applications / Date published
568807000 Additional ring containing 9
20110124924Cyclopropanation Process - A method for the preparation of cyclopropyl carbinols by cyclopropanation of unsaturated alcoholates, utilising a reagent system selected from (A) magnesium metal and dibromomethane, and (B) dibromomethane and a tertiary Grignard reagent, the reaction being carried out in the presence of an ether solvent.05-26-2011
20110313203METHOD FOR PURIFYING CRUDE POLYMETHYLOLS - The present invention relates to a process for purifying crude polymethylol which comprises polymethylol of the formula (I)12-22-2011
20160002133NOVEL PROCESS FOR GENERATING HEMP OIL WITH A HIGH CANNABIDIOL (CBD) CONTENT - A method for producing hemp oil, comprising decarboxylation of CBDA in hemp oil; short-path evaporation of CBD from the decarboxylated hemp oil to produce CBD oil; selective THC to CBN conversion performed on the decarboxylated hemp oil.01-07-2016
568808000 Polycyclo ring system 4
20100081849REACTION SYSTEM - The invention provides a reaction system comprising: a first reaction promoter capable of converting a first substrate into a first substance; and a plurality of microcapsules, each of said microcapsules comprising a second reaction promoter encapsulated within an encapsulant, said second reaction promoter being capable of converting a second substrate into a second substance. The second substrate is capable of passing through the encapsulant to contact the second reaction promoter and the second substance is capable of passing out of the microcapsules through the encapsulant. In the reaction system, either (a) the first substance is, or is capable of being converted into, the second substrate and, in operation, the conversion of the second substrate by the second reaction promoter occurs to a greater extent than the conversion of the first substrate by the second reaction promoter and the conversion of the second substance by the first reaction promoter is low, or (b) the second substance is, or is capable of being converted into, the first substrate and, in operation, the conversion of the first substrate by the first reaction promoter occurs to a greater extent than the conversion of the second substrate by the first reaction promoter and the conversion of the first substance in the microcapsules is low.04-01-2010
20100197976CATALYSTS - Catalysts suitable for asymmetric hydrogenation reactions is described comprising the reaction product of a group 8 transition metal compound a chiral phosphine and a chiral diamine of formula (I)08-05-2010
20130041185FULLERENE DERIVATIVE, METHOD FOR PRODUCING THE SAME, AND ALLERGEN ADSORBENT USING THE SAME - Provided are a novel fullerene derivative which can adsorb quickly and efficiently an allergen which may cause a pollen allergy without releasing the allergen again, does not contain a metal or the like which may cause a harmful effect to a human body, and is easily applicable, impregnable, or chemically bondable onto surface of various materials; and a process for producing the same. The fullerene derivative is characterized in that a halogen group and many hydroxyl groups are bonded directly to a fullerene nucleus. In the case that the halogen group is chlorine, the fullerene derivative can be synthesized by a partial hydroxylation of a chlorinated fullerene or a partial chlorination of a hydroxylated fullerene.02-14-2013
20150291492THE CROSS COUPLING OF 2-BROMO-1-PHENYL INDENES WITH PHENYL ACETYLENES AND OTHER SUBSTITUTED ACETYLENES IN WATER - The cross-coupling reaction of 2-bromo-1-phenyl indenes with phenyl acetylenes or propargyl alcohol is disclosed. The cross-coupling reaction uses a palladium catalyst with triphenylphosphine in the absence of a copper co-catalyst. The reaction is carried out with pyrrolidine as the base in water at 120° C.10-15-2015
568809000 Plural benzene rings bonded directly to the same carbon 2
20080300430IRIDIUM CATALYSTS FOR CATALYTIC HYDROGENATION - The present disclosure relates to a process for the reduction of compounds comprising one or more carbon-oxygen (C═O) double bonds, to provide the corresponding alcohol, comprising contacting the compound with hydrogen gas at a pressure greater than 3 atm and a catalyst comprising an iridium aminodiphosphine complex.12-04-2008
20120088938METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL - Disclosed is a method for producing an optically active alcohol including reacting a titanium compound, an aromatic magnesium compound and a carbonyl compound in the presence of an optically active biphenol compound having a predetermined structure and an ether compound having a predetermined structure.04-12-2012

Patent applications in all subclasses Additional ring containing

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