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Class 568/645 - Halogen containing


Subclass of Class 568 - Organic compounds -- part of the class 532-570 series
Definition: Compounds which contain halogen.
No. of patents: 133
Last issue date: 05/22/2007


1        
NumberTitleIssue Date
7220784Substituted stilbenes and their reactions
The present invention relates to stilbene and quinone compounds related to combretastatin A-4 and their use as anticancer compounds and prodrugs. The compounds include those with an alkyl group on the double bond of cis or trans-stilbenes, compounds with one or more...
05/22/2007
7193019Process for the production of vinyl compound
A process for the production of a vinyl compound of the formula (1), which process comprises reacting a bifunctional phenylene ether oligomer of the formula (2) with a vinylbenzyl halide ...
03/20/2007
7109245Vasoconstrictor cannabinoid analogs
Methods and compounds for reversing pathological vasodilation of blood vessels, for example vasodilation caused by activation of CB1-like receptors, by administering to a subject a therapeutically effective amount of a compound sufficient to induce vasoconstriction,...
09/19/2006
7077960Method for obtaining a purified hydrofluoroalkane, purified hydrofluoroalkane, use of same and method for analysing same
Process for the production of a hydrofluoroalkane, according to which hydrofluoroalkane comprising organic impurities is subjected to at least two distillations. ...
07/18/2006
6958423Bromination process
This invention relates to a novel process which comprises feeding a mixture formed from diphenylethane and bromine to a stirrable reaction mass comprised of bromine and a bromination catalyst to yield a decabromodiphenylethane wet cake which can be most economically...
10/25/2005
6936739Fluorine-containing bisphenols, their preparation, their precursors and intermediates, and use of the fluorine-containing bisphenols
This invention relates to 1,2-di(4-hydroxyaryl)tetrafluoroethanes of the general formula (I) wherein R are each, independently of one another, hydrogen, F, Cl, Br, I, CN, COOR2, C1-C
08/30/2005
6864397Difluoromethyl ether derivative and process for producing the same
The present invention provides a process for producing a difluoromethyl ether derivative simple and efficient process for producing the difluoromethyl ether derivative represented by Formula (1d′) or a difluoromethyl ether derivative represented by Formula (1c′)...
03/08/2005
6844462Biphenydiols
The invention relates to the biphenyldiols of the formula (V) The corresponding racemic and enantiomerically pure triflate compounds thereof, where R1 and R2 are H, R3 is chlorine, and R
01/18/2005
6767923Benzhydryl derivatives
Benzhydryl derivatives of the formula I, where the index and the variables are as defined below: X is oxygen or sulfur; R1, R3 are halogen, cyano, nitro, hydroxyl, mercapto, amino, alk...
07/27/2004
6689922Vitamin D analogues
The invention concerns novel bi-aromatic compounds having the formula: ##STR1## which are analogs of vitamin D, the process of preparing them, as well as their use in pharmaceutical compositions in human or veterinary medicine, particularly in dermatology...
02/10/2004
6635787Production method of a 2,6-dichlorophenol compound
A 2,6-dichlorophenol compound of formula (1): ##STR1## wherein R represents a 3,3-dihalo-2-propenyl group or a benzyl group optionally substituted by halogen atom(s), can be produced by making a phenol compound of formula (2): ##STR2## wherein R has ...
10/21/2003
63426421,4-diaryl-2-fluoro-1-buten-3-ol compounds and their use in the preparation of 1,4-diaryl-2-fluoro-1,3-butadiene and 1,4-diaryl-2-fluoro-2-butene compounds
The present invention provides novel 1,4-diaryl-2-fluoro-1-buten-3-ol compounds of the structural formula I ##STR1## a method for the preparation of those formula I compounds, and the use of those formula I compounds in the preparation of 1,4-diaryl-...
01/29/2002
6333437Method for purifying a bromine compound
A method for purifying a bromine compound by depositing the bromine compound represented by the following general formula (1) as solid particles from a crude solution containing the bromine compound: ##STR1## wherein (i) the crude solution is supplied int...
12/25/2001
6278028Liquid crystal compounds, mixtures and devices
An electroclinic device having two spaced cell walls each bearing electrode structures and treated on at least one facing surface with an alignment layer, a layer of a smectic liquid crystal material enclosed between the cell walls, where the liquid cryst...
08/21/2001
6235870Dehydrohalogenation of poly (phenylhalo-b-hydroxypropyl ether) to form polyepoxide
Process for the preparation of compounds of the formula ##STR1## wherein Hal represents chlorine, bromine or iodine and preferably chlorine, wherein Ra represents hydrogen or a residue comprising one or more additional groups of the formula, ...
05/22/2001
6207835Process for the preparation of arylmetal compounds and their reaction with electrophilic reagents
Arylmetal compounds are prepared by deprotonation of aromatics which have a hydrogen atom in the ortho position relative to a halogen atom or a trifluoromethoxy group, using a suitable base or by halogen-metal exchange of haloaromatics using a suitable me...
03/27/2001
6005063Epoxy compounds from chlorohydrin ethers of polyphenols
Process for the preparation of compound of the formula: ##STR1## wherein Rc represents a residue comprising one or more additional groups of the formula: ##STR2## by heating a compound of the formula (A) ##STR3## at a temper...
12/21/1999
6001954Process for the manufacture of epoxy compounds
Process for the preparation of compounds of the formula ##STR1## wherein Hal represents chlorine, bromine or iodine and preferably chlorine, wherein Ra represents hydrogen or a residue comprising one or more additional groups of the formul...
12/14/1999
5868960Mesomorphic compound, liquid crystal composition containing the compound, liquid crystal device using the composition, liquid crystal apparatus and display method
A mesomorphic compound of the formula (I) according to Claim 1 characterized by having at least two ether groups between alkylene groups in a specific alkoxy perfluoroalkyl terminal group is suitable as a component for a liquid crystal composition providi...
02/09/1999
5654331Diaromatic compounds derived from a salicylic unit and their use in human and veterinary medicine and in cosmetics
Diaromatic compounds, characterised in that they correspond to the following general formula: ##STR1## in which: R1 is --CH3, --CH2 OH, --COR8 or --CH2 OCOR9, R8 is H, OH, -...
08/05/1997
5618849Orally active antiviral compounds
A compound represented by formula I Ar1 --O--M--O--Ar2 I wherein Ar1 and Ar2 are independently substituted phenyl or substituted pyridinyl, the substituents on said phenyl or pyridinyl being ...
04/08/1997
5559133Orally active antiviral compounds
A compound represented by formula I, Ar1 --O--M--O--Ar2, wherein Ar1 and Ar2 are independently substituted phenyl or substituted pyridinyl, the substituents on said phenyl or pyridinyl being independently select...
09/24/1996
5457235Halogenated diphenyldiacetylene liquid crystals
The present invention provides liquid crystals that are diphenyldiacetylenes of the general formulas: ##STR1## where W, X, Y and Z are, independently of one another, a halogen atom, a hydrogen atom or a trihalomethyl group, T1 and T2
10/10/1995
5422035Benzene derivatives, and liquid-crystalline medium
A liquid-crystalline medium based on a mixture of polar compounds having positive dielectric anisotropy, comprising one or more compounds of the formula I ##STR1## in which R, A1,. A2, Z1, Z2, m, n, L1...
06/06/1995
5366656Optically active alcohol and derivatives thereof, liquid crystal composition containing same and liquid crystal device
Optically active compounds of general formulae ##STR1## wherein A is O or S, R1 is a hydrogen atom, an alkyl group having 1-22 carbon atoms, a hydroxy containing alkyl group, para-alkyl substituted phenyl, para-alkyl substituted biphenyl, ...
11/22/1994
5350772Certain substituted phenoxy-methyl phenyl-methoxy benzenes having antiviral activity
A compound represented by formula I Ar1 --O--M--O--Ar2 I wherein Ar1 and Ar2 are independently substituted phenyl or substituted pyridinyl, the substituents on said phenyl or pyridinyl being ...
09/27/1994
5340498Anti-ferroelectric liquid crystal and liquid crystal display device
A novel anti-ferroelectric liquid crystal of the formula (I), ##STR1## wherein: is an integer of 3 to 8, each of X and Y is independently a hydrogen atom or a fluorine atom, Z is --CF3, --CH3 or --C2 H5, q is 0 or 5,...
08/23/1994
5324449Substituted phenyl trifluoromethyl ethers
Substituted phenyl trifluoromethyl ethers of the formula I R1 --(A1 --Z1)n --A2 --Z2 --A3 --OCF3 I in which R1, A1
06/28/1994
5302619Aromatic compounds, their production processes and their compositions for the control of insect pests
Aromatic compounds are disclosed of the formula: ##STR1## wherein R1 is a C3 -C8 alkyl group, a C3 -C8 alkoxy group, an alkoxyalkyl group having 3 to 8 carbon atoms, a C3 -C8
04/12/1994
5279764Dihalogenobenzene derivatives
The invention relates to dihalogenobenzene derivatives of the formula I R1 --A1 --Z1 --A2 --(Z2 --A3)n --R2 wherein R1, R2, A1, A2, A...
01/18/1994
5278215Flame-retardant synthetic resin composition and flame retardant
A flame-retardant synthetic resin composition containing (A) a synthetic resin and (B) a compound having a 3-halogeno-2-hydroxypropyl group, which shows excellent thermal stability during molding and having good light resistance, is disclosed. A flame ret...
01/11/1994
5274002Trisubstituted phenyl analogs having activity for congestive heart failure
Novel trisubstituted phenyl analogs are now found to have activity as for the treatment of congestive heart failure....
12/28/1993
52484472,3-difluorohydroquinone derivatives
2,3-difluorohydroquinone compounds of the formula I ##STR1## in which R1 and R2, in each case independently of one another, are alkyl having 1 to 15 C atoms or alkenyl having 3 to 15 C atoms which are unsubstituted, monosubstitu...
09/28/1993
5242996Modified epoxy resins having acetylenically unsaturated functions
A modified epoxy resin or compound of the formula: ##STR1## wherein A is the backbone reside of a glycidyl ether epoxy resin with removal of the glycidyloxy groups; R1 and R2 are independently a hydrogen atom or C1 -C...
09/07/1993
5238603Optically active liquid crystalline compound and a composition containing same
A liquid crystal compound having specific features suitable to use for a display mode utilizing ferroelectric liquid crystals, particularly a large spontaneous polarization value and a liquid crystal composition using the compound are provided, which comp...
08/24/1993
5210278Process for the preparation of bisarylalkyl ethers
A process for preparing a substituted styrene by reacting a bisarylalkyl ether in the presence of an acid catalyst is disclosed. The process is preferably used for the preparation of 4-acetoxystyrene from 4,4'-(oxydiethylidene)bisphenol diacetate and 4-me...
05/11/1993
5196586Polydiphenyldiacetylenes
Disclosed herein are polydiphenyldiacetylenes having the following repeating unit (III): ##STR1## (wherein R1 denotes a hydrogen atom or a methoxy group; R2 denotes a hydrogen atom, a methoxy group or a methylamino group; R...
03/23/1993
5149858Selective ortho-chlorination of phenols
Phenolic compounds, notably admixtures of 2,4-dichlorophenol and 2,6-dichlorophenol, are selectively chlorinated at the ortho positions thereof, with gaseous chlorine and in a molten medium, in the presence of a selectivity-enhancing effective amount of a...
09/22/1992
5132328Alcohol and ether derivatives
The invention concerns a compound of the formula I, ##STR1## wherein Ar1 is optionally substituted phenyl or naphthyl; A1 is (1-6C)alkylene, (3-6C)alkenylene, (3-6C)alkynylene or cyclo(3-6C)alkylene; Ar2 is optionally subs...
07/21/1992
5130048Ferroelectric liquid crystal compositions containing chiral haloalkoxy tails units
The subject application discloses a chiral nonracemic composition of the general formula: R1 --Ar--O--CH2 --C*HX--C*HY--CH2 --O--R2 wherein R1 is an achiral tail of two to sixteen carbons; Ar is an achiral...
07/14/1992
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