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WO/2010/084976A1 |
Disclosed is a method for manufacturing a conjugated aromatic compound, which is characterized in that an aromatic compound (A), wherein one or two leaving groups selected from a group comprised of an iodine atom, bromine atom and chlori...
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WO/2010/082558A1 |
Disclosed is a liquid crystalline compound which is stable toward heat, light or the like, exhibits a nematic phase in a broad temperature range, has a small viscosity, large optical anisotropy and a proper coefficient of elasticity (K33...
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WO/2010/083101A1 |
The present invention relates to a group of new plasticizers for thermoplastics such as polypropylene, copolymers of polypropylene, polyethylene, polyethylene terephthalates, polystyrene and/or other polymers or mixtures of polymers cont...
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WO/2010/069898A1 |
The present invention relates to defoaming compositions comprising compounds having the formula C5H11CH(CH2CH2CH3)CH2O(CH2CH(X)O)nH (I) where X=(CH2)aCH3 where a= 0 or 1 and where n=0.5-5; and one or more hydrotropes selected from the gr...
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WO/2010/069133A1 |
Disclosed is a preparing process of methanol, dimethyl ether and lower olefin from synthesis gas, which comprises contacting synthesis gas with catalyst under the conditions of the conversion of synthesis gas to methanol, dimethyl ether ...
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WO/2010/068183A1 |
There is provided a glucose-PEG conjugate comprising a PEG moiety conjugated to a linear glucose moiety at the C1 position of the glucose moiety. The glucose-PEG conjugate may be used to reduce glucose transport into a cell and may be us...
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WO/2010/062486A2 |
A method of making a fluorinated ether includes combining, in a polar aprotic solvent: a fluorinated alcohol represented by the formula X-Rf1CH2OH, and a fluorinated sulfonate ester represented by the formula Rf2CH2OS(=O)2Rf3, and base; ...
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WO/2010/060566A1 |
In a method for producing dimethyl ether (DME) from methanol (MeOH) by converting raw MeOH obtained through MeOH synthesis to DME in a reactor, separating water in the process, the raw MeOH and a process-internally obtained return flow f...
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WO/2010/060048A2 |
Compounds of Formula (I): R1-O-(CF2-O)n-R1, wherein: n is an integer from 2 to 100; and R1 is perfluorinated alkyl or substituted perfluorinated alkyl are described. Also described are methods of preparing the compounds of Formula (I). F...
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WO/2010/057691A2 |
Hydrofluoro alcohols of formula : A-(Rf)a-CFX-O-RhO-(CFX-(Rf)a*-CFX-O-RhO-)nH (I) in which : Rh is a hydrocarbon-based chain; X is F or a C1-C6 (per)fluoroalkyl; a or a* is 0 or 1; Rf is a (per)fluoro(poly)oxyalkylene chain or a (per)flu...
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WO/2010/054540A1 |
Disclosed is a method for preparing chloromethyl-1,1,1,3,3,3-hexafluoroisopropyl ether, which is combining hexafluoroisopropanol and either 1,3,5-trixane or paraformaldehyde in the presence of a binary catalyst system to produce chlorom...
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WO/2010/048715A1 |
The invention relates to gemini surfactants of formula IA wherein A is a core derived from an organic polyhydroxy compound; R1 and R2 are each independently a hydrophobic group; and R3 and R4 are each independently a surfactant head grou...
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WO/2010/050427A1 |
Disclosed is a liquid crystal composition suitable for producing a liquid crystal electrooptical element which can be driven at a low voltage in a wide temperature range and has high display quality. Also disclosed is a liquid crystal e...
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WO/2010/049465A1 |
A process for the preparation of acylated secondary alcohol alkoxylates, said process comprising : (i) reaction of one or more internal olefins with one or more carboxylic acids in the presence of a catalyst composition in order to form ...
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WO/2010/047335A1 |
Disclosed is a benzene compound represented by any one of general formulae (A) to (D). The benzene compound can emit light efficiently in a solid state. (In general formula (A), RA1 and RA2 independently represent an amino group, or the...
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WO/2010/048170A2 |
This disclosure relates to reagents and methods useful in the synthesis of aryl fluorides, for example, in the preparation of 18F labeled radiotracers. The reagents and methods provided herein may be used to access a broad range of compo...
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WO/2010/046926A2 |
The present invention relates to Stilbene derivatives of the general formula I or a pharmaceutically acceptable salt thereof have properties such as high water solubility, bioavailability and effective as carcinostatics.
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WO/2010/047712A1 |
Intermediates and synthetic processes for the preparation of substituted phenylalanine-based compounds (e.g., of Formula I) are disclosed:
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WO/2010/044940A2 |
Polyfluorene polymers and copolymers having substantial amounts (10-100%) of fluorenes coupled at the 2 and 5 positions of fluorene are useful as active layers in OLED devices where triplet energies > 2.10 eV are required.
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WO/2010/040730A1 |
The present invention discloses new analogs of polysphorin and their uses as antimalarial drugs which are highly effective in the hepatic phase of the disease. The present invention further discloses a new method for preparing these comp...
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WO/2010/041748A1 |
Disclosed is a prophylactic or therapeutic agent for diabetes, diabetic complications, insulin resistance syndrome, metabolic syndrome, hyperglycemia, dyslipidemia, atherosclerosis, heart failure, cardiomyopathy, myocardial ischemia, cer...
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WO/2010/041253A1 |
The present invention relates compositions comprising (3R, 4R, 6R)-stereoisomers of phenyl substituted pinenes having CB receptor agonists properties, uses thereof for the manufacture of pharmaceutical compositions and processes for thei...
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WO/2010/034999A1 |
A compound of formula (I) in solid form, preferably crystalline form.
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WO/2010/035000A1 |
Using a combination of Kumada, Suzuki and Biellmann chemistry, various menaquinones can synthesised rapidly and with stereochemical integrity offering a new way of preparing these vitamin K2 components for the pharmaceutical market. In o...
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WO/2010/036555A2 |
Provided are foam control agents and their use for controlling foam in fermentation processes. The foam control agents are of the formula I: wherein R1, R2, R3, R4, n and y are as defined above.
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WO/2010/031611A1 |
The invention relates to a method for producing stilbenoids, comprising the following steps: I) bringing a cell, which is able to form stilbenoids, in contact with a nutrient medium comprising at least one polyether, and II) cultivating ...
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WO/2010/033976A2 |
A process for preparing a detergent alcohol mixture comprising the steps of providing one or more poly-branched poly-olefins, wherein the poly-branched poly-olefins must contain one non-branched terminal olefin and one or more additional...
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WO/2010/029462A1 |
The present invention provides divinyl ether derivatives capable of releasing in a controlled manner at least one active aldehyde and/or ketone into the surrounding environment. The invention relates to the use of these divinyl ether der...
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WO/2010/029998A1 |
Provided are a method for producing a (poly)glycerol monobenzyl ether which makes it possible to obtain a (poly)glycerol monobenzyl ether with high yield and selectivity in an etherification reaction of a benzyl alcohol and (poly)glycero...
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WO/2010/030096A2 |
This invention relates to a glycerol-ester-based plasticizer, particularly to a plasticiser for polyvinyl chloride, and plastics containing the same. More specifically, this invention relates to a plasticiser prepared by esterification r...
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WO/2010/029923A1 |
Provided is a method for producing a perfluoro compound having hydroxyl groups, with which there is unlikely to be any aggregation of the reduction intermediate during reduction and wherein a perfluoro compound having –C(=O)OH can be u...
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WO/2010/026962A1 |
Provided are fluorine-containing adamantane derivatives represented by general formula (I) that provide cured products, which are suitable as electronic and optical materials and have superior heat resistance, mar resistance, low refract...
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WO/2010/027663A1 |
New polyol ether compounds and a process for their preparation. The process comprises reacting a polyol, a carbonyl compound, and hydrogen in the presence of hydrogenation catalyst, to provide the polyol ether. The molar ratio of polyol ...
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WO/2010/022645A1 |
The present application provides a preparation method of fluoromethyl 1,1,1,3,3,3-hexafluoroisopropyl ether by reacting CH2FX with 1,1,1,3,3,3-hexafluoroisopropanol in the presence of acid-binding agent. The reaction can be also performe...
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WO/2010/024139A1 |
Disclosed is a compound for organic thin film transistors, which has a structure represented by formula (1). (In formula (1), at least one of R1-R6 represents a substituent, and the rest represent hydrogen atoms.)
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WO/2010/024388A1 |
A compound for organic thin film transistors, which is represented by formula (1).In formula (1), at least a pair of adjacent two groups among R1, R3, R5 and R7 combine together to form a substituted or unsubstituted aromatic hydrocarbon...
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WO/2010/023317A1 |
The present invention relates to novel hexafluoro-2-biphenylisopropanol compounds corresponding to general formula (I) below, in which R1, R2, R3, R4 and R5 are as defined in the description, and also to the method for the preparation th...
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WO/2010/020903A1 |
The present invention concerns the process for producing liquid polyols of renewable origin from organic materials such as agro-forestry and agro-food biomass and respective industrial residues, constituting a profitable and bio-friendly...
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WO/2010/020561A1 |
The present invention relates to a method for isolating ditrimethylol propane from secondary trimethylol propane production streams.
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WO/2010/022269A2 |
A process for the preparation of dibutoxymethane, in one embodiment from 50% formaldehyde, in a condensation reaction without the use of co-solvent.
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WO/2010/019360A2 |
In an improved process for telomerizing butadiene, contact butadiene and an organic hydroxy compound represented by formula ROH (I), wherein R is a substituted or unsubstituted C1-C20-hydrocarbyl and the organic hydroxy compound is not g...
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WO/2010/015559A1 |
Disclosed is a process for the preparation of a mixture of 4-bromophenyl derivatives (compound of formula (2)) and 2,4-dibromophenyl derivatives (compound of formula (3)) comprising the steps of [1] reacting in a two-phase (liquid-liquid...
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WO/2010/016511A1 |
Disclosed is a compound for organic thin film transistors, which has a structure represented by formula (1). [In formula (1), R1-R6 each represents a hydrogen atom, a halogen atom, an alkyl group having 1-30 carbon atoms, a haloalkyl gro...
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WO/2010/014936A2 |
A manufacturing process for making terameprocol (1) which includes the following reaction scheme, wherein a first general reaction is the formation of a furan intermediate (39) and a second general reaction is the ring-reduction and ring...
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WO/2010/013724A1 |
Disclosed is a compound containing a divalent group represented by formula (I). (In formula (I), Ar1 represents an arylene group, a divalent heterocyclic group or a divalent aromatic amine group; J1 represents a phenylene group; J2 repre...
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WO/2010/011504A2 |
The invention provides a method for producing methanol and its products exclusively from a geothermal source as the sole source material also using the needed energy from the geothermal energy source. The method includes separating or is...
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WO/2010/010287A2 |
The invention relates to a method for producing dialkoxy alkanes by direct partial oxidation of a lower alcohol with a catalyst based on mixed oxide containing molybdenum and at least one other metal selected from the metals that can ass...
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WO/2010/006402A1 |
The invention provides a method of converting glycerol to oxygenates (i.e. one or more oxygen-containing hydrocarbons) of lower boiling point than glycercol itself. The method involves reaction of glycerol with an alcohol under reduced p...
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WO/2010/000136A1 |
The invention provides a method of synthesizing sevoflurane. The method comprises the following steps that: taking hexafluoro isopropanol as the raw material and reacting it with trioxymethylene (or paraformaldehyde) in the presence of ...
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WO/2010/002622A1 |
A compound comprising Formula 5: RfOCFHCF2O(CH2CH2O)v-H, wherein Rf is CcF(2c+1); c is 2 to about 6; and v is 2 to about 4; and a process for its preparation comprising contacting a compound of Formula 6: Rf-O-CF=CF2, wherein Rf is CcF(2...
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