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The phosphorus is in a ring

Subclass of:

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

558000000 - ORGANIC COMPOUNDS (CLASS 532, SUBCLASS 1)

558070000 - Phosphorus esters (i.e., compounds having the phosphorus ester group, wherein trivalent or pentavalent phosphorus and carbon are bonded directly to the same divalent chalcogen, and wherein the carbon may be single bonded to any atom but may be multiple bonded only to carbon)

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Class / Patent application numberDescriptionNumber of patent applications / Date published
558073000 The phosphorus is in a ring 28
20110124899METHOD FOR PREPARING COMBRETASTATIN - The Invention relates to a method for preparing a combretastatin (A): formula (I) in the form of a base or of an addition salt with an acid, which comprises coupling, in the presence of a base and of T3P, the salt of the (Z)-amino compound of formula (II) with a doubly protected L-serine derivative of formula (III) in which PG denotes a group protecting the amine function, so as to obtain the compound of formula (Z)-(Ib): formula (IV), then deprotecting and opening the ring of (Z)-(Ib) in the presence of an acid, so as to obtain the combretastatin (A) in the form of a salt; and, optionally, adding a base, so as to obtain the combretastatin (A) in the form of a base, the salt of the (Z)-amino compound having been obtained by enrichment of the salt of the amino compound of formula (V) in (Z) isomer.05-26-2011
558076000 Additional phosphorus containing ring 16
20080287701BISBIPHENYLACYLPHOSPHINE OXIDE AND PREPARATION METHOD THEREFORE - A bisbiphenylacylphosphine oxide of formula (I) and its preparation method are provided. The formula of —Ar— is11-20-2008
20120149932PHOSPHORUS-CONTAINING COMPOUNDS USEFUL FOR MAKING HALOGEN-FREE, IGNITION-RESISTANT POLYMERS - Phosphorus-containing compounds useful for flame retardant epoxy resins are disclosed. The flame retardant epoxy resins may be used to make electrical laminates. This invention is particularly useful in end use applications in which a low bromine or low halogen content is required or desired.06-14-2012
20130296597PHOSPHORUS-CONTAINING OLIGOMER AND METHOD FOR PRODUCING THE SAME, CURABLE RESIN COMPOSITION AND CURED PRODUCT OF THE SAME, AND PRINTED WIRING BOARD - A phosphorus-containing oligomer is represented by formula (1):11-07-2013
20140357885DOPO DERIVATIVE FLAME RETARDANTS - The present invention relates to novel, halogen-free flame retardant derived from 9,10-Dihydro-9-Oxa-10-Phosphaphenantrene-10-oxide (DOPO). This invention also relates to the use of the halogen free DOPO derived flame retardant in polymers.12-04-2014
20150126762PROCESS FOR THE PREPARATION OF DOPO-DERIVED COMPOUNDS AND COMPOSITIONS THEREOF - This invention relates to a process for producing compounds derived from 9,10-Dihydro-9-Oxa-10-Phosphaphenantrene-10-oxide (DOPO). In particular, the invention relates to producing DOPO-derived compounds by reacting DOPO with diol compounds in the presence of a catalyst. This invention also relates to DOPO derived composition containing a high melting point diastereomer. The DOPO derived compounds may be useful as flame-retardants.05-07-2015
20150344507PHOSPHORUS-CONTAINING COMPOUNDS USEFUL FOR MAKING HALOGEN-FREE, IGNITION-RESISTANT POLYMERS - Phosphorus-containing compounds useful for flame retardant epoxy resins are disclosed. The flame retardant epoxy resins may be used to make electrical laminates. This invention is particularly useful in end use applications in which a low bromine or low halogen content is required or desired.12-03-2015
558077000 Phosphorus, and two chalcogens bonded directly thereto, in the same ring (e.g., cyclic phosphonates, etc.) 10
20130317246METHOD FOR THE PURIFICATION OF BIPHEPHOS - The invention relates to a process for the purification of 6,6′-[(3,3′-di-tert-butyl-5,5′-dimethoxy-1,1′-biphenyl-2,2′diyl)bis(oxy)]bis(dibenzo[d,f][1,3,2]dioxaphosphepin), abbreviation: biphephos (see formula 1).11-28-2013
20150073169PURIFICATION PROCESS - A process for reducing the level of contaminant metals in ligands used in the preparation of catalysts is disclosed.03-12-2015
558078000 Acyclic divalent chalcogen single bonded directly to the ring phosphorus (e.g., cyclic phosphites, etc.) 8
20130041171MACROMOLECULAR ANTIOXIDANTS BASED ON STERICALLY HINDERED PHENOLS AND PHOSPHITES - A sterically hindered phenol and phosphite based compound represented by the following formula:02-14-2013
20130324756METHOD FOR THE PREPARATION OF BIPHEPHOS - The invention relates to a process for producing 6,6′-[(3,3′-di-tert-butyl-5,5′-dimethoxy-1,1′-biphenyl-2,2′diyl)bis(oxy)]bis(dibenzo[d,f][1,3,2]dioxaphosphepine), abbreviated to biphephos (see formula 1), with low chlorine content12-05-2013
20140288322Preventing Solvent of Crystallization in Production of Polyphosphite Ligands - Residual wash solvent, e.g., ethyl acetate, is removed from polyphosphite, e.g., bisphosphite, crystals by a process comprising the steps of: A. Mixing the polyphosphite crystals and residual wash solvent with a secondary alcohol, e.g., isopropyl alcohol (IPA), to form a mixture of polyphosphite crystals, residual wash solvent and secondary alcohol, and B. Drying the mixture to remove the residual wash solvent and secondary alcohol to a content of less than 0.5 wt % based on the weight of the polyphosphite crystals.09-25-2014
20140350280EXTRACTION SOLVENT CONTROL FOR REDUCING STABLE EMULSIONS - Disclosed herein are methods for recovering diphosphite-containing compounds from mixtures comprising organic mononitriles and organic dinitriles, using liquid-liquid extraction. Also disclosed are treatments to enhance extractability of the diphosphite-containing compounds.11-27-2014
20160159840BISPHOSPHITES HAVING AN UNSYMMETRIC OUTER BIPHENOL UNIT - Bisphosphites having at least one unsymmetric outer biphenol unit are useful for the hydroformylation of an olefin.06-09-2016
558079000 And divalent chalogen double bonded directly to the ring phosphorus (e.g., cyclic phosphates, etc.) 3
20110207955Process for the production of organic dithiopyrophosphates - Organic dithiopyrophosphates of formula wherein R08-25-2011
20120264965PROCESSES FOR PRODUCTION OF CYCLIC ALKYLENE PHOSPHOROHALIDITE AND CYCLIC PHOSPHORIC ACID ESTER - A process for producing a cyclic alkylene phosphorohalidite, which comprises reacting a specific phosphorus trihalide with a specific alkylene glycol compound under conditions where the phosphorus trihalide is present in an excess amount relative to the amount of the alkylene glycol compound in the reaction system to order to obtain the cyclic alkylene phosphorohalidite by reacting the alkylene glycol compound with the phosphorus trihalide; and a process for producing a cyclic phosphoric acid ester by using the obtained cyclic alkylene phosphorohalidite as a raw material.10-18-2012
201400666461,3,2-Dioxaphosphorinane, 2-Sulfide Derivatives For Use As Anti-Wear Additives In Lubricant Compositions - The present disclosure relates to a non-acidic, sulfur-containing, phosphorus-containing compound of the formula I03-06-2014
558080000 And nitrogen in the ring 1
558081000 And chalcogen or carbon in the ring 1
20110207956INTRAMOLECULAR C-H AMINATION WITH PHOSPHORYL AZIDES - A highly effective Co(II)-based system has been developed for catalytic intramolecular C—H amination with phosphoryl azides without the need of terminal oxidant or other additives, resulting in the high-yielding production of cyclophosphoramidates with nitrogen gas as the by-product; additional features of this new catalytic system include the amination of primary C—H bonds and formation of 7-membered ring structures.08-25-2011
558082000 And carbon and chalcogen in the ring 10
20100069657METHOD FOR THE PRODUCTION OF DIBENZ[C,E] [1,2]-OXAPHOSPHORIN DERIVATIVES, AMINO-DIBENZ[C,E] [1,2]-OXAPHOSPHORIN AND ALSO USE THEREOF - The invention relates to general syntheses of (6H)-dibenz[c,e] [1,2]-oxaphosphorins which are substituted with nitrogen compounds on the phosphorus atom and comprising commercially available 6H-dibenz[c,e] [1,2]-oxaphosphorin-6-oxides. These nitrogen-containing (6H)-dibenz[c,e] [1,2]-oxaphosphorins can be used as reactive starting substances for further syntheses or as flameproofing agents or as stabilisers.03-18-2010
20100105939PHOSPHORUS-CONTAINING COMPOUND AND METHOD FOR PREPARING THE SAME - The present invention provides a phosphorus-containing compound of formula (I):04-29-2010
20110034717METHOD FOR SYNTHESIZING 9,10-DIHYDRO-9-OXA-10-PHOSPHAPHENANTHRENE-10-OXIDE AND DERIVATIVES THEREOF - A method for synthesizing 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide or its derivatives has a step of introducing 6-chloro-6H-dibenz[c,e][1,2]oxaphosphorin or its derivative, an acid compound and water into a reacting chamber to form an organic layer having 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide or its derivative and an aqueous layer. Because the acid compound is from an external source and has a catalyzing effect, employing the method can prevent side reaction from occurring and increase yield of 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide or its derivative. Furthermore, the method is a one-pot operation of hydrolysis, dehydration and cyclization, so the method does not require purification of intermediates. Therefore, the method is time-and cost-saving and requires less organic solvent, resulting in less pollution to the environment.02-10-2011
20140235886PHOSPHORUS-BASED (METH)ACRYLATE COMPOUND AND METHOD OF PREPARING THE SAME - This invention relates to a novel compound having high refractive index suitable for use in optical resin materials, etc., without containing a sulfur atom, and to a method of preparing the same, in which the compound is a phosphorus-based (meth)acrylate compound represented by Formula (I).08-21-2014
558083000 Plural chalcogens in the ring 6
20090326256ANALGESIC AGENT COMPRISING CYCLIC PHOSPHATIDIC ACID DERIVATIVE - An object of the present invention is to elucidate an analgesic effect as one of new cPA bioactivities and thus to provide a novel analgesic agent. The present invention provides an analgesic agent which comprises a cyclic phosphatidic acid derivative that is one type of phospholipid.12-31-2009
20150045572PROCESS FOR THE PREPARATION OF PHOSPHINIC ACID ESTERS - The invention relates to a process for the preparation of alkyl phosphinates, alkenyl phosphinates, alkynyl phosphinates or phenyl phosphinates by reaction of a corresponding phosphine oxide with an alcohol or phenol in the presence of alkali-metal fluoride or tetraalkylammonium fluoride.02-12-2015
558084000 The ring phosphorus is attached directly to halogen or an acyclic nitrogen by nonionic bonding 2
20110201837METHOD FOR PRODUCING 6-CHLORODIBENZO[D,F] [1,3,2]DIOXAPHOSPHEPIN - The invention relates to a method for producing 6-chlorodibenzo[d,f] [1,3,2]-dioxaphosphepin (formula 1), comprising the following steps: a) addition of liquid 2,2′-dihydroxybiphenyl into a reactor to an excess of phosphorous trichloride under inert gas and stirring; b) discharge and neutralization of the resulting gases from the reaction mixture; c) separation of the excess phosphorous trichloride; d) obtention of 6-chlorodibenzo[d,f] [1,3,2]-dioxaphosphepin.08-18-2011
20130172596PROCESS FOR PREPARING 6-CHLORODIBENZO[D,F][1,3,2]DIOXAPHOSPHEPIN - The present invention relates to a process for preparing 6-chlorodibenzo[d,f][1,3,2]dioxaphosphepin (I)07-04-2013
558085000 Acyclic divalent chalcogen single bonded directly to the ring phosphorus (e.g., cyclic phosphites, etc.) 2
558086000 And divalent chalcogen double bonded directly to the ring phosphorus (e.g., cyclic phosphates, etc.) 2
20130072708PHOSPHORIC ACID ESTER PRODUCTION METHOD - The present invention provides a novel production method which enables obtain a phosphorus compound having both an aromatic substituent and a phosphorinane backbone, without using an expensive hydrogen halide scavenger, without going through a complicated post treatment step or a step of recovering a solvent, and with a favorable yield andpurity. In the present invention, step (1) of allowing phosphorus oxytrihalide to react with a phenol compound or naphthol compound at a molar ratio of 1.1-3.0:1 in the presence of metal halide, and removing unreacted phosphorus oxytrihalide, to produce a mono-substituted phosphorodihalidate; and step (2) of allowing the mono-substituted phosphorodihalidate obtained in the step (1) to react with a diol compound, at a 0.90 to 0.99 molar equivalent based on 1 mole of the halogen atom in the mono-substituted phosphorodihalidate so as to perform a dehydrohalogenation reaction, to obtain a phosphorus compound represented by Formula (V).03-21-2013
20160152551PROCESS FOR THE PREPARATION OF CLOMIPHENE06-02-2016
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