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Inventor:
Romer; Duane R.
Address:
Midland, MI
No. of patents:
23
Patents:




Patent Number Title Of Patent Date Issued
7553917 Technique for selecting polymerization modifiers cross reference statement June 30, 2009
A combinatorial method for identifying a catalyst composition for use in the homogeneous addition polymerization of an olefin monomers, said catalyst composition comprising a transition metal compound, a cocatalyst and a polymerization modifier, as well as catalyst compositions and i
7214638 Olefin polymerization catalyst composition comprising group 13 amide derivatives May 8, 2007
Catalyst compositions that are highly tolerant of catalyst poisons for use in addition polymerizations comprising a catalytic derivative of a Group 4 metal complex, a cocatalyst, and a Group 13 metal amide compound.
6329528 Process for preparing 3-(substituted phenyl)-5-thienyl or furyl)-1,2,4-triazoles and novel inter December 11, 2001
New synthetic procedures for preparing insecticidal 3-(substituted phenyl)-5-(thienyl or furyl)-1,2,4-triazoles utilizing thioimidate intermediate.
6288188 Polyphenylene oligomers and polymers September 11, 2001
An oligomer, uncured polymer or cured polymer comprising the reaction product of one or more polyfunctional compounds containing two or more cyclopentadienone groups and at least one polyfunctional compound containing two or more aromatic acetylene groups wherein at least some of the
5965679 Polyphenylene oligomers and polymers October 12, 1999
An oligomer, uncured polymer or cured polymer comprising the reaction product of one or more polyfunctional compounds containing two or more cyclopentadienone groups and at least one polyfunctional compound containing two or more aromatic acetylene groups wherein at least some of the
5885991 Thiocyanomethyloxy (and thiocyanothiomethyl)-1,2,3-benzatriazin-4(3H) ones, compositions contain March 23, 1999
Disclosed are thiocyanomethyloxy(or thiocyanomethylthio)-1,2,3-benzatriazin-4(3H)-one compounds corresponding to one of the formulae: ##STR1## wherein Z represents oxygen or sulfur; X represents --C1, --F, --I, C.sub.1 -C.sub.7 straight or branched chain alkyl, C.sub.1 -C.sub.7
5723486 1,3 dithiolo(4,5)-1,3-dithiolo-2-thione derivatives, compositions and use as antimicrobial and m March 3, 1998
Disclosed are 1,3-dithiolo(4,5-d)-1,3-dithiino-2-thione compounds corresponding to one of the formulae: ##STR1## wherein R.sup.1 represents --Br, --Cl, --F, --CN or --CH(CH.sub.2).sub.n CH.sub.3 and n is an integer of from 0 to 10.These compounds as well as the unsubstituted compound
5703114 Use of 4,5-dicyano-1-3-dithiole-2-one (or thione) as antimicrobial and marine antifouling agents December 30, 1997
Disclosed is the use of compositions employing a 4,5-dicyano-1,3-dithiole-2-one (or thione) compound corresponding to the formula: ##STR1## wherein Z is oxygen or sulfur as the active antimicrobial and marine antifouling agent.
5703102 1,2,5-thiadiazolo-1,3-dithiole-2-one (or thione) as antimicrobial and marine antifouling agents December 30, 1997
Disclosed are compositions containing 1,2,5-thiadiazolo-1,3-dithiole-2-one or thione corresponding to the formula: ##STR1## wherein Z is oxygen or sulfur and the use thereof as antimicrobial and marine antifouling agents.
5661176 (2-one (or thione)-1,3-dithiole-4,5-diyl)-bis(thiomethylthiocyanate), compounds for use as antim August 26, 1997
Disclosed are (2-one (or thione)-1,3-dithiole-4,5-diyl)bis(thiomethylthiocyanate) compounds corresponding to the formula: ##STR1## wherein Z is oxygen or sulfur, compositions containing said compounds and their use as antimicrobial and marine antifouling agents.
5661165 ((4-phenyl-1,2,5-thiadiazol-3-yl)oxy)methyl ester thiocyanic acid compounds, compositions contai August 26, 1997
Disclosed are ((4-phenyl-1,2,5--thiadiazol-3-yl)oxy)methyl ester thiocyanic acid compounds corresponding to the formula: ##STR1## wherein X represents --Br, --Cl, --F, --CF.sub.3, --OCF.sub.3, --CN, C.sub.1 -C.sub.7 straight or branched chain alkyl, C.sub.1 -C.sub.7 straight or b
5633219 5H-pyrrolo(3',4':5,6)(1,4)dithiin o(2,3-C)(1,2,5)thiadiazole-5,7(6H)-dione, compositions containi May 27, 1997
Various 5H-pyrrolo(3',4':5,6)(1,4) dithiino-(2,3-C)(1,2,5)thiadiazole-5,7(6H)-diones corresponding to the formula ##STR1## wherein R represents --H, benzyl, phenethyl, a C.sub.1 -C.sub.10 straight or branched chain alkyl radical, a C.sub.3 -C.sub.10 cycloalkyl radical, a C.su
5631277 (2-one (or thione)-1,3-dithiole 4,5-diyl) bis(thiocyanate) compounds, compositions containing th May 20, 1997
Disclosed is (2-thione-1,3-dithiole 4,5-diyl) bis(thiocyanate), its preparation and its use as an antimicrobial and marine antifouling agent.
5631207 Use of 5-alkyl-1,3,4-oxadiazol (and thiadiazol)-2-thiomethylthiocyanates as marine antifouling a May 20, 1997
Disclosed is the use of compositions employing 5-alkyl-1,3,4-oxadiazol(or thiadiazol)-2-thiomethylthiocyanates as the active marine antifouling agent.
5491155 Substituted thiadiazoles, compositions containing them and their use as antimicrobial and marine February 13, 1996
Substituted thiadiazoles which correspond to the formula: ##STR1## wherein X and Y each independently represents --Br, --Cl, --OCH.sub.3, --SCN, --OCH.sub.2 SCN, --SCH.sub.2 SCN, --OCH.sub.2 CH.sub.2 SCN or --SCH.sub.2 CH.sub.2 SCN, provided that at least one of X or Y represents
5488060 Substituted thiadiazoles, compositions containing them and their use as antimicrobial and marine January 30, 1996
Substituted thiadiazoles which correspond to the formula: ##STR1## wherein R represents ##STR2## X represents --Br, --Cl, --F, --CH.sub.3, --OCH.sub.3, --COOCH.sub.3, --NO.sub.2, --SCH.sub.3, --SO.sub.2 CH.sub.3 or --CF.sub.3 and Y is --SCN or --SCH.sub.2 SCN.These compounds
5488051 Substituted 5,6-dihydro-5-oxo-1,4-dithiino-(2,3-d)-pyridazine-2,3-dicarbonitriles, compositi January 30, 1996
Substituted 5,6-dihydro-5-oxo-1,4-dithiino-(2,3-d)-pyridazine-2,3-dicarbonitriles are prepared which correspond to the formula: ##STR1## wherein R represents ##STR2## wherein X.sup.1 is Cl, Br, NO.sub.2 or CH.sub.3, y is 0 or 1 and n is 0, 1 or 2.These compounds have been
5466707 Dimercapto-1,3-dithiolo-2-one or thione maleimides, compositions containing them and their use a November 14, 1995
Various 4,5-dimercapto-1,3-dithiolo-2-one or thione maleimides corresponding to the formula ##STR1## wherein R represents --H, phenyl, benzyl, phenethyl, a C.sub.1 -C.sub.10 straight or branched chain alkyl radical, a C.sub.3 -C.sub.10 cycloalkyl radical, a C.sub.1 -C.sub.10 stra
5466707 Dimercapto-1,3-dithiolo-2-one or thione maleimides, compositions containing them and their use a November 14, 1995
Various 4,5-dimercapto-1,3-dithiolo-2-one or thione maleimides corresponding to the formula ##STR1## wherein R represents --H, phenyl, benzyl, phenethyl, a C.sub.1 -C.sub.10 straight or branched chain alkyl radical, a C.sub.3 -C.sub.10 cycloalkyl radical, a C.sub.1 -C.sub.10 stra
5455222 1-substituted-5-thiomethylthiocyanato-1H-tetrazoles, compositions containing them and their use October 3, 1995
Disclosed are substituted-5-thiomethylthiocyanato-1H-tetrazole compounds corresponding to the formula ##STR1## wherein R represents a C.sub.1 -C.sub.6 straight or branched chain alkyl radical, a C.sub.3 -C.sub.6 cycloalkyl or a phenyl radical of the formula ##STR2## wherein e
5334603 Composition and use of 3-phenyl-5-thiocyano-methylthio-1,3,4-thiadiazole-2(3h)thione August 2, 1994
A compound is prepared which corresponds to the formula: ##STR1## This compound has been found to exhibit antimicrobial activity in industrial and commercial applications and compositions containing this compound are so employed.
5200409 Composition and use of substituted 1,3-dithiolo-and 1,4-dithiinoquinoxalines as an antimicrobial April 6, 1993
Substituted 1,3-dithiolo- and 1,4-dithiinoquinoxalines are prepared which correspond to the formula: ##STR1## wherein X represents: ##STR2## and R.sup.1 and R.sup.2 independently represent hydrogen, halogen, nitro, cyano, alkyl, alkoxy, arylcarbonyl, or an alkoxy carbonyl gro
5180740 Composition and use of dimercapto-substituted dinitriles as an antimicrobial January 19, 1993
Dimercapto-substituted dinitriles are prepared which correspond to the formula: ##STR1## wherein X represents: ##STR2## These compounds have been found to exhibit antimicrobial activity in industrial and commercial applications and compositions containing these compounds


 
 
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