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Nitriles (i.e., compounds having cyano bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

Subclass of:

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

558000000 - ORGANIC COMPOUNDS (CLASS 532, SUBCLASS 1)

Patent class list (only not empty are listed)

Deeper subclasses:

Class / Patent application numberDescriptionNumber of patent applications / Date published
558308000 Processes for forming the cyano group 91
558435000 Acyclic (e.g., purification of saturated nitriles, etc.) 47
558332000 Processes of attaching cyano to carbon by reaction of an inorganic cyanide with an organic compound (e.g., using HCN, cyanogen, metal cyanide, ammonium cyanide, cyanogen chloride, etc.) 41
558411000 Benzene ring bonded directly to the cyano group 31
558388000 Benzene ring attached indirectly to the cyano group by acyclic nonionic bonding 18
558357000 Processes of forming carbon to carbon bond between carbons of two organic reactants 17
558426000 Benzene ring attached indirectly to the cyano group by nonionic bonding (i.e., alicyclic ring between the benzene ring and the cyano group) 10
558428000 Polycyclo alicyclic ring system containing 9
558355000 Isomerization processes (e.g., double bond shift, cis-trans isomerism, etc.) 7
558353000 Processes utilizing carbon monoxide as a reactant 4
20140088321PROCESS FOR PRODUCING ALDEHYDE COMPOUNDS - A process for producing an aldehyde compound of the invention comprising: reacting a compound represented by the following formula (a1) or (a2) with a hydrogen and a carbon monoxide in a presence of a compound containing a metal belonging to Groups 8 to 10 and a phosphorous compound so as to satisfy the following conditions (1) and (2) to synthesize an aldehyde compound; 03-27-2014
20150291513PURIFICATION METHOD OF ALDEHYDE COMPOUND - The purification method of an aldehyde compound of the present invention includes a step of neutralizing a reaction solution containing an aldehyde compound by adding water and a base compound to the reaction solution, and a step of distilling the neutralized reaction solution, in which the reaction solution is obtained by reacting a compound represented by the following Formula (a1) or (a2) with hydrogen and carbon monoxide in the presence of a metal compound of groups 8 to 10 and a phosphorus compound, the phosphorus compound is represented by Formula (R10-15-2015
20150299108PREPARATION METHOD OF ALDEHYDE COMPOUND - A preparation method of an aldehyde compound of the present invention includes a step of reacting the compound represented by the following general formula (a1) or (a2) with hydrogen and carbon monoxide in the presence of a metal compound including 0.01 ppmmol to 10 ppmmol of a metal belonging to Groups 8 to 10 with respect to 1 mole of the compound and a phosphorus compound, and the amount of a chlorine portion in the reaction system in the step is equal to or less than 1.5 parts by weight with respect to 1 part by weight of the metal belonging to Groups 8 to 10.10-22-2015
20150299109PREPARATION METHOD OF ALDEHYDE COMPOUND - A preparation method of an aldehyde compound of the present invention includes a step of reacting a compound represented by the following general formula (a1) with hydrogen and carbon monoxide in the presence of a metal compound including 0.01 ppmmol to 10 ppmmol of a metal belonging to Groups 8 to 10 with respect to 1 mole of the compound and a phosphorus compound, and in the step, the amount of acrylonitrile included in the compound represented by the general formula (a1) is equal to or less than 200-fold by mole with respect to 1 mole of the metal belonging to Groups 8 to 10.10-22-2015
558384000 Boron or spiro containing 3
20160111648Spirally Configured Cis-Stilbene/Fluorene Hybrid Materials for Organic Light-Emitting Diode - The present invention provides a series of spirally configured cis-stilbene/fluorene hybrid materials, which are spirally-configured cis-stilbene/fluorene derivatives having glass transition temperatures ranged from 105° C. to 130° C., decomposition temperatures ranged from 385° C. to 415° C., reversible electron transport property, and balanced charges motilities. Moreover, a variety of experimental data have proved that the yellow fluorescent, the green phosphorescent, the yellow phosphorescent, and the red phosphorescent OLEDs using this spirally configured cis-stilbene/fluorene derivatives as the electron transport layers having hole blocking functions can indeed show excellent EQE, current efficiency, power efficiency, maximum luminance, and device lifetime performances much better than the conventional or commercial yellow fluorescent, green phosphorescent, yellow phosphorescent, and red phosphorescent OLEDs.04-21-2016
20160130285METHOD FOR PRODUCING SALTS HAVING HYDRIDOCYANOBORATE ANIONS - The invention relates to a method for producing alkali metal salts having monohydrido-tricyanoborate anions from alkali metal monofluorotricyanoborates, and to a method for producing alkali metal salts having dihydrido-dicyanoborate anions from alkali metal difluorodicyanoborates.05-12-2016
20160130286METHOD FOR PRODUCING SALTS HAVING MONOFLUORO-TRICYANOBORATE ANIONS - The invention relates to a method for producing alkali metal salts having monofluoro-tricyanoborate anions from alkali metal tetrafluoroborates.05-12-2016
558385000 Phosphorus attached indirectly to the cyano group by nonionic bonding 2
20090240073METHOD FOR DETOXIFYING PHOSPHONATE HERBICIDES - The invention relates in general to methods for detoxifying phosphonate herbicides. The methods may comprise transacetylating the phosphonate herbicide. The phosphonate herbicides can comprise a CP bond and a CN bond and may be glyphosate.09-24-2009
20130204031PROCESS OF PRODUCING PHOSPHINOTHRICIN EMPLOYING NITRILASES - The present invention generally relates to processes for the enzymatic production of a phosphinothricin product or precursor thereof from a nitrile-containing substrate.08-08-2013
558304000 With preservative or stabilizer 2
20140121399Quinone Compounds for Inhibiting Monomer Polymerization - The polymerization of monomers may be at least partially reduced or inhibited by introducing an effective amount of an additive. The additive may be or include a first compound:05-01-2014
20120203020MULTI-COMPONENT POLYMERIZATION INHIBITORS FOR ETHYLENICALLY UNSATURATED MONOMERS - The invention provides a composition and a method of using the composition for inhibiting the unwanted polymerization of ethylenically unsaturated monomers. The composition is prepared by reducing a nitroxide stable free radical to its corresponding hydroxylamine through reaction with a dialkyl/aryl hydroxylamine and subsequent addition of a polymerization prevention component selected from phenolic antioxidants, phenylenediamine and phenylenediamine derivatives, or phenothiazine and phenothiazine derivatives targeted towards ethylenically unsaturated monomers. The conversion of the nitroxide by the dialkyl/aryl hydroxylamine is to prevent it or the polymerization prevention component from being “spent” by reaction with each other, impurities or any other incompatible components. This allows previously incompatible combinations to now work effectively. In fact, the combination is more efficacious as the combination exerts a synergy due to the presence of various polymerization prevention reagents. The composition is a synergistic combination of various polymerization inhibition compounds for the inhibition of the unwanted polymerization of ethylenically unsaturated monomers.08-09-2012
558430000 Six-membered alicyclic ring containing 2
20110137065PROCESSES FOR SYNTHESIZING 1-(2-ETHYLBUTYL)CYCLOHEXANE CARBONITRILE - Processes are provided for synthesizing substituted cyclohexane carbonitriles, particularly 1-(2-ethylbutyl)cyclohexane carbonitrile. Such processes comprise deprotonizing cyclohexane carbonitrile with chloro magnesium N,N-diisopropylamide and alkylating the deprotonated cyclohexane carbonitrile in the presence of 2-(ethylbutyl) bromide to produce 1-(2-ethylbutyl)cyclohexane carbonitrile.06-09-2011
20140114085PROCESS FOR PREPARING 3-CYANO-3,5,5-TRIMETHYLCYCLOHEXANONE - The present invention refers to the preparation of 3-cyano-3,5,5-trimethylcyclohexanone (isophorone nitrile, abbreviation IPN) using a calcium alkoxide, particularly calcium ethoxide, as catalyst.04-24-2014
558354000 Racemization, resolution, or inversion of configuration processes for optically active compounds 2
20080306296Process for the resolution of racemic verapamil - A new process is described for the resolution of racemic verapamil, which allows the desired enantiomer to be obtained in high yields and with high enantiomeric purity. The process uses optically active 2,3-bis[(2-fluorobenzoyl)oxy]butanedioic acid as the resolving agent, and a water/dimethylformamide or water/acetonitrile or water/methanol mixture, as the reaction solvent.12-11-2008
20100204503Stereoselective Bioconversion of Aliphatic Dinitriles into Cyano Carboxylic Acids - The present invention is directed to a regio- and stereoselective bioconversion of selected aliphatic dinitriles into corresponding cyanocarboxylic acids. More particularly, the present invention provides methods for the conversion of 2-isobutyl-succinonitrile into (S)-3 cyano-5-methylhexanoic acid, which is a useful intermediate in the synthesis of (S)-3(aminomethyl)-5-methylhexanoic acid (pregabalin). Pregabalin can be used for treating certain cerebral diseases, for example, in the treatment and prevention of seizure disorders, pain, and psychotic disorders.08-12-2010
558379000 Processes of forming an acyclic or alicyclic carbon to carbon double bond from an existing acyclic or alicyclic carbon to carbon single bond (e.g., by dehydroacylation, etc.) 1
20100029978RAPIDLY CURING CYANOACRYLATES AS ADHESIVES - The present invention relates to a polymerizable adhesive composition which comprises, at least as one constituent, a cyanacrylate component and which requires a comparitively short time for curing when used on surfaces. The present invention therefore also includes a method for the production of the cyanacrylate component described above, and the cyanacrylate component as such.02-04-2010
558434000 Three-membered alicyclic ring containing 1
20120310003METHOD FOR PRODUCING CYANOALKENYLCYCLOPROPANECARBOXYLIC ACID SALT - A method for producing a salt of an amine with a cyanoalkenylcyclopropanecarboxylic acid, the method comprising a first step of mixing a carboxylic acid compound represented by formula (2C) and at least one amine selected from the group consisting of primary amines and secondary amines in an organic solvent; a second step of depositing a salt of the amine with a cyanoalkenylcyclopropanecarboxylic acid represented by formula (2) from the mixture obtained in the first step; and a third step of recovering the salt deposited in the second step;12-06-2012
Entries
DocumentTitleDate
20080214857Method Of Reducing A Functional Group In An Oxidized Form - A novel method of reducing a functional group in an oxidised form. The invention relates more particularly to the reduction of aldehyde, ketone, ester, lactone, nitrile or phosphine oxide groups. The reduction method according to the invention is characterised in that it comprises exposing the substrate including the functional group to be reduced to the presence of a siloxane-type compound of the following formula (I), combined with a Lewis acid-type catalyst. In said formula (I):—R1 and R2, which are the same or different, are an alkyl, cycloalkyle or aryl group, —X is a digit from 0 to 50.09-04-2008
20090171109Integrated process for preparing a carboxylic acid from an alkane - The present invention relates to an integrated process for producing unsaturated carboxylic acids from the corresponding C07-02-2009

Patent applications in all subclasses Nitriles (i.e., compounds having cyano bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

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