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2614 results about "Trifluoromethyl" patented technology

Trifluoromethyl is a functional group that has the formula -CF₃. The naming of is group is derived from the methyl group (which has the formula -CH₃), by replacing each hydrogen atom by a fluorine atom. Some common examples are trifluoromethane H–CF₃, 1,1,1-trifluoroethane H₃C–CF₃, and hexafluoroacetone F₃C–CO–CF₃. Compounds with this group are a subclass of the organofluorines.

Inhibitors of P2X3

Compounds of formula 1 are modulators of P2X3 useful for the treatment of pain and genito-urinary, gastrointestinal, and respiratory disorders:
wherein
    • R1 is —C(═S)CH3, pyridyl, pyrimidinyl, pyrazinyl, thiazolyl, furyl, furylcarbonyl, acetyl, or carbamoyl; R2a and R2b are independently H, methyl, or ethyl; R3 is H or methyl; Y is a bond, —(CR4R5)n— or —CR4═CR5—; wherein R4 and R5 are each independently H or methyl and n is 1 or 2; X is N or CH; A is phenyl, 5-membered heterocyclyl, or 6-membered heterocyclyl; R6, R7 and R8 are each independently H, halo, lower alkyl, cycloalkyl, alkylthio, alkylthio-lower alkyl, alkylsulfonyl-lower alkyl, di(lower alkyl)amino-lower alkyl, morpholinyl-lower alkyl, 4-methyl-piperazinyl-methyl, trifluoromethyl, pyridyl, tetrazolyl, thiophenyl, phenyl, biphenyl, or benzyl (where thiophenyl, phenyl and benzyl are substituted with 0-3 lower alkyl, halo, sulfonamido, trifluoromethyl, lower alkoxy or lower alkylthio) or R6 and R7 together form a 5-membered or 6-membered carbocyclic or heterocyclic ring substituted with 0-3 substituents selected from the group consisting of lower alkyl, lower alkoxy, oxo, halo, thiophenyl-lower alkyl, phenyl, benzyl (where phenyl and benzyl are substituted with 0-3 lower alkyl, halo, sulfonamido, trifluoro-methyl, lower alkoxy, lower alkylthio, amino-lower alkyl, lower alkylamino-lower alkyl, or di(lower alkyl)amino-lower alkyl); and pharmaceutically acceptable salts thereof; wherein when R1 is pyrimidin-2-yl, X is N, Y is a bond and A is oxazol-5-yl the carbon atom at position 4 in said oxazol-5-yl is not substituted by propyl when the carbon atom at position 2 in said oxazol-5-yl is substituted by substituted phenyl and the carbon atom at position 4 in said oxazol-5-yl is not substituted by phenyl when the carbon atom at position 2 is substituted by unsubstituted or substituted phenyl.
Owner:ROCHE PALO ALTO LLC

Phenyl derivatives containing an acidic group, their preparation and their use as chloride channel blockers

InactiveUS6417393B1Reduced cell volumeBiocideUrea derivatives preparationArylHydrogen
The present patent application relates to compounds having formula (I) or a pharmaceutically acceptable salt thereof wherein one of R1, R2 and R3 is a non-cyclic acidic group having a pKa value below 8 or a group which is in vivo convertible to such a group; R4, R5 and the other two of the substituents R1, R2 and R3 are each independently selected from hydrogen, alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, alkoxy, hydroxy, halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro, amnino, and aryl, aralkyl, arylamino, aryloxy, aryl-CO-, or heteroaryl, wherein the aryl and heteroaryl groups may be substituted one or more times with substituents selected from alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, hydroxy, alkoxy, halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro and amino; or R3 and R4 or R4 and R5 together form a fused 4- to 7-membered carbocyclic ring which may be unsaturated, or partially or fully saturated, while the other substituents R1, R2, R3, R4 and R5 are as defined above; Y is -CO-, -CS-, -SO2-, or -C(=N-R8)-, wherein R8 is hydrogen, alkyl, or cyano; X is -NH-, -CH2-NH-, or -SO2-NH-; Z is NR6, O, -CH=CH-, -C=C-, -N=CH-, or -CH=N-; wherein R6 is hydrogen, or alkyl; R11, R12, R13, R14 and R15 are each independently selected from hydrogen, alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, alkoxy, hydroxy, halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro, amino, -NHSO2-R7, -COOR7, -SO2N(R7)2, -SO2OR7 and -CO-R7, wherein R7 is hydrogen alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, aryl or aralkyl; and aryl, aralkyl, arylamino, aryloxy, aryl-CO-, or heteroaryl, wherein the aryl and heteroaryl groups may be substituted one or more times with substituents selected from alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, hydroxy, alkoxy, halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro and amino; or one of R11 and R12, R12 a
Owner:ANIONA APS

Nonaqueous electrolyte and nonaqueous electrolyte secondary battery using the same

A nonaqueous electrolyte containing a silicon compound of formula (1) or (2) and a nonaqueous electrolyte secondary battery using the nonaqueous electrolyte and excellent in cycle characteristics and low temperature characteristics,
wherein R1 and R2 each represent alkyl, cycloalkyl, alkoxy or halogen; R3 represents alkenyl; and X represents halogen,
wherein R4, R5, R6, and R7 each represent alkyl, alkoxy, alkenyl, alkenyloxy, alkynyl, alkynyloxy, phenyl or phenoxy, each of which may have an ether bond in its chain; R8 represents halogen, halogen-substituted aryl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl; a trifluoromethyl group, an acyloxy group having 5 to 8 carbon atoms, a sulfonate group having 1 to 8 carbon atoms, an isocyanyl group an isothianyl or a cyano group, R9 represents halogen, a trifluoromethyl group,an acyloxy group having 5 to 8 carbon atoms, a sulfonate group having 1 to 8 carbon atoms, an isocyanyl group an isothianyl or a cyano group: halogen-substituted aryl; n represents 1 or 2; and Y represents a single bond, oxygen, alkylene, alkylenedioxy, alkenylene, alkenylenedioxy, alkynylene, alkynylenedioxy, arylene or arylenedioxy; provided that the number of groups having an unsaturated bond in R4, R5, R6, R7, R8, and R9 is zero or one.
Owner:DENSO CORP +1

Lithium ion battery electrolyte with both high and low temperature performances

The invention relates to the technical field of lithium ion electrolytes, and in particular relates to a lithium-ion battery electrolyte with both high and low temperature performances. The electrolyte comprises lithium hexafluorophosphate, mixed organic solvents, filming additives, additives for improving the dielectric constant and the low temperature infiltration capability, and a lithium salt type additive, wherein the mixed organic solvents comprise a carbonic ester solvent and a linear carboxylic ester solvent; the linear carboxylic ester solvent in the mixed organic solvents is one or a mixture of more than two of ethyl propionate, propionic acid n-propyl ester, n-propyl acetate, acetic acid n-butyl ester and isobutyl acetate; and the additives for improving the dielectric constant and the low temperature infiltration capability are one or a mixture of more than two of fluoro ethylene carbonate, difluoro ethylene carbonate and 4-trifluoromethyl ethylene carbonate. A battery prepared from the lithium-ion battery electrolyte with both high and low temperature performances is long in service life, and both the good low temperature discharge performance of the battery is ensured, and the storage performance of the battery at the high temperature of 60 DEG C is effectively considered.
Owner:DONGGUAN SHANSHAN BATTERY MATERIALS
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