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Browse by: INVENTOR PATENT HOLDER PATENT NUMBER DATE
 
 
Inventor:
Hall; John B.
Address:
Rumson, NJ
No. of patents:
141
Patents:


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Patent Number Title Of Patent Date Issued
4686310 2-isopropenyl-5-methylcyclopentanealkanols derivatives and organoleptic uses or same August 11, 1987
Described are the 2-isopropenyl-5-methylcyclopentanealkanols and esters thereof having the generic structure: ##STR1## wherein R.sub.1 represents hydrogen or C.sub.2 -C.sub.3 acyl and wherein n represents 0 or 1 and uses thereof in augmenting or enhancing the aroma of consumable
4650898 Uses of methyl phenyl pentanol derivatives in augmenting or enhancing the aroma or taste of cons March 17, 1987
Described are 2-methyl-4-phenyl-1-pentanol derivatives defined according to the structure: ##STR1## wherein R represents hydrogen or acetyl and uses thereof in augmenting or enhancing the aroma or taste of consumable materials including perfume compositions, colognes, perfumed ar
4632831 Uses of methyl phenyl pentanol derivatives in augmenting or enhancing the aroma or taste of cons December 30, 1986
Described are 2-methyl-4-phenyl-1-pentanol derivatives defined according to the structure: ##STR1## wherein R represents hydrogen or acetyl and uses thereof in augmenting or enhancing the aroma or taste of consumable materials including perfume compositions, colognes, perfumed ar
4627935 2-isopropenyl-5-methylcyclopentanealkanols, esters thereof and organoleptic uses of same December 9, 1986
Described are the 2-isopropenyl-5-methylcyclopentanealkanols and esters thereof having the generic structure: ##STR1## wherein R.sub.1 represents hydrogen or C.sub.2 -C.sub.3 acyl and wherein n represents 0 or 1 and uses thereof in augmenting or enhancing the aroma of consumable
4610812 Uses of methyl phenyl pentanol derivatives in augmenting or enhancing the aroma or taste of cons September 9, 1986
Described are 2-methyl-4-phenyl-1-pentanol derivatives defined according to the structure: ##STR1## wherein R represents hydrogen or acetyl and uses thereof in augmenting or enhancing the aroma or taste of consumable materials including perfume compositions, colognes, perfumed ar
4609754 Process for the production of isosolanone and solanone, intermediates useful in said process and September 2, 1986
Described is a novel genus of compounds defined according to the structure: ##STR1## wherein Z represents hydrogen, MgX and the moiety having the structure: ##STR2## and X represents chlor, bromo, or iodo; as well as 5-isopropyl-8-methyl-5,8-nonadien-2-one; uses of same as interm
4576740 Tertiary pentamethylindanol derivatives and organoleptic uses thereof March 18, 1986
Described are tertiary pentamethylindanol derivatives defined according to the structure: ##STR1## wherein the dashed line represents a carbon-carbon single bond or a carbon-carbon double bond and uses thereof in augmenting or enhancing the aroma or taste of consumable materials
4576186 Use of pentamethylindanol derivatives in augmenting or enhancing the aroma or taste of smoking t March 18, 1986
Described are tertiary pentamethylindanol derivatives defined according to the structure: ##STR1## wherein the dashed line represents a carbon-carbon single or a carbon-carbon double bond and uses thereof in augmenting or enhancing the aroma or taste of smoking tobaccos or smokin
4560499 Isosolanone and solanone intermediates and organoleptic uses December 24, 1985
Described is a novel genus of compounds defined according to the structure: ##STR1## wherein Z represents hydrogen, MgX and the moiety having the structure: ##STR2## and X represents chloro, bromo or iodo; as well as the novel compounds defined according to the structures: ##
4549982 1-Oxoalkyl-2-isopropylnorbornane derivatives, uses thereof in augmenting or enhancing the aroma October 29, 1985
Described are 1-oxoalkyl-2-isopropylnorbornane derivatives defined according to the generic structure: ##STR1## wherein X represents a moiety selected from the group consisting of: ##STR2## wherein the dashed line represents a carbon-carbon double bond or a carbon-carbon sing
4548821 Flavoring with tertiary pentamethylindanol derivatives October 22, 1985
Described are tertiary pentamethylindanol derivatives defined according to the structure: ##STR1## wherein the dashed line represents a carbon-carbon single bond or a carbon-carbon double bond and uses thereof in augmenting or enhancing the aroma or taste of consumable materials
4541951 1(1,3-Dioxobutane)-3,3-dimethylcyclohexane useful in perfumes September 17, 1985
Described is a process for preparing the compound having the structure: ##STR1## comprising the steps of reacting 1-acetyl-3,3-dimethylcyclohexane having the structure: ##STR2## with an alkyl acetate defined according to the structure: ##STR3## wherein R.sub.2 is C.sub.1
4535192 Tertiary pentamethylindanol derivatives and organoleptic uses thereof August 13, 1985
Described are tertiary pentamethylindanol derivatives defined according to the structure: ##STR1## wherein the dashed line represents a carbon-carbon single bond or a carbon-carbon double bond and uses thereof in augmenting or enhancing the aroma or taste of consumable materials
4520032 Use in augmenting or enhancing the aroma or taste of foodstuffs or chewing gums of tetrahydro-1, May 28, 1985
Described are tertiary pentamethylindanol derivatives defined according to the structure: ##STR1## wherein the dashed line represents a carbon-carbon single bond or a carbon-carbon double bond and uses thereof in augmenting or enhancing the aroma or taste of consumable materials
4503258 Process for preparing 1(4-pentenoyl)-3,3-dimethylcyclohexane and intermediates used in said proc March 5, 1985
Compounds of the following structure ##STR1## wherein R.sub.1 is selected from the group consisting of hydrogen and 2-propenyl are disclosed useful as intermediates in organic synthesis.
4501762 Process for preparing acyl trimethyl cyclohexene derivatives and use of intermediates therefor i February 26, 1985
Described is a process for preparing .beta.-damascone starting with 2,6,6-trimethyl cyclohex-2-enone according to the reaction sequence: ##STR1## wherein Z is hydrogen, MgX', Li, Na or K; Y is MgX', Li, Na or K; X' is Cl, Br or I; R is C.sub.1 -C.sub.3 lower alkyl such as methyl, eth
4476147 Flavoring of alliaceous-flavored foodstuffs October 9, 1984
A process for augmenting or enhancing the aroma or taste of alliaceous flavors, particularly garlic flavors, by augmenting or enhancing the garlic and green aroma and taste nuances of alliaceous-flavored foodstuffs comprising the step of adding to a alliaceous-flavored foodstuff an aroma
4458699 Uses of methyl phenyl pentanol derivatives in augmenting or enhancing the aroma or taste of smok July 10, 1984
Described is the use of compounds defined according to the structure: ##STR1## wherein R represents hydrogen or acetyl in augmenting or enhancing the aroma or taste of smoking tobacco compositions or smoking tobacco articles.
4458093 Hexadienoyl cyclohexene derivative July 3, 1984
Described is the hexadienoyl cyclohexene derivative defined according to the structure: ##STR1## which may either be in the form of a mixture of Z, Z; E, E; Z, E or E, Z isomers or the individual isomers themselves having the structures: ##STR2## a process for preparing same,
4450101 Organoleptic compositions with substituted tricyclodecane compounds May 22, 1984
Described are substituted tricyclodecane derivatives having the generic structure: ##STR1## wherein Y is a moiety having a structure selected from the group consisting of: ##STR2## wherein one of the dashed lines represents a carbon-carbon single bond and the other of the
4449007 Process for preparing 1(4-pentonoyl)-3,3-dimethylcyclohexane and intermediates used in a said pr May 15, 1984
A process comprising the steps of reacting 1-acetyl-3,3-dimethylcyclohexane with an alkyl acetate, thereby forming a diketone having the structure: ##STR1## reacting the said diketone with an allyl halide to form a substituted diketone having the structure: ##STR2## which is
4433695 Process for the production of isosolanone and solanone, intermediates useful in said process and February 28, 1984
A process for augmenting or enhancing the aroma or taste of a smoking tobacco or smoking tobacco article comprising the step of adding to a smoking tobacco or smoking tobacco article component, an aroma or taste augmenting or enhancing quantity of a mixture of cis and trans isomers of
4430508 Substituted tricyclodecane derivatives, processes for producing same and organoleptic uses there February 7, 1984
Described are substituted tricyclodecane derivatives having the generic structure: ##STR1## wherein Y is a moiety having a structure selected from the group consisting of: ##STR2## wherein one of the dashed lines represents a carbon-carbon single bond and the other of the
4428966 Use of substituted cyclohexyl carboalkoxy ketone in augmenting or enhancing the aroma or taste o January 31, 1984
Described is a process for augmenting or enhancing the aroma or taste of raspberry flavored foodstuffs or chewing gums by adding to a foodstuff or chewing gum an aroma or taste augmenting or enhancing quantity of at least one compound having the structure: ##STR1## wherein R repr
4418010 Substituted tricyclodecane derivatives, processes for producing same and organoleptic uses there November 29, 1983
Described are substituted tricyclodecane derivatives having the generic structure: ##STR1## wherein Y is a moiety having a structure selected from the group consisting of: ##STR2## wherein one of the dashed lines represents a carbon-carbon single bond and the other of the
4413139 Intermediates used in the process for preparing 1(4-pentenoyl)-3,3-dimethylcyclohexane November 1, 1983
Described is a process for preparing the compound having the structure: ##STR1## comprising the steps of reacting 1-acetyl-3,3-dimethylcyclohexane with a dialkyl carbonate; thereby forming a ketoester having the structure: ##STR2## wherein R represents C.sub.1 -C.sub.3 lower alky
4410740 Substituted tricyclodecane derivatives, processes for producing same and organoleptic uses there October 18, 1983
Described are substituted tricyclodecane derivatives having the generic structure: ##STR1## wherein Y is a moiety having a structure selected from the group consisting of: ##STR2## wherein one of the dashed lines represents a carbon-carbon single bond and the other of the
4386023 Substituted tricyclodecane derivatives, processes for producing same and organoleptic uses there May 31, 1983
Described are substituted tricyclodecane derivatives having the generic structure: ##STR1## wherein Y is a moiety having a structure selected from the group consisting of: ##STR2## wherein one of the dashed lines represents a carbon-carbon single bond and the other of the
4385072 Use of esters of 1-acetyl cyclohexanol in augmenting or enhancing the aroma or taste of foodstuf May 24, 1983
Described is a process for augmenting or enhancing the aroma or taste of foodstuffs and chewing gums comprising the step of adding to a foodstuff composition or chewing gum composition, an aroma or taste augmenting or enhancing quantity of at least one of the two compounds having the
4374055 Alkyl esters of 1-alkanoyl cycloalkanols and organoleptic uses thereof February 15, 1983
Described is a process for preparing several substituted or unsubstituted cycloalkyl acyl alkanoates defined according to the generic structure: ##STR1## wherein R.sub.1 and R.sub.2 taken together complete a cycloalkyl moiety or methyl, dimethyl or trimethyl substituted cycloalkyl mo
4359395 Process for enhancing the organoleptic properties of perfumed articles using alkyl esters of 1-a November 16, 1982
Described is a process for preparing several substituted or unsubstituted cycloalkyl acyl alkanolates defined according to the generic structure: ##STR1## wherein R.sub.1 and R.sub.2 taken together complete a cycloalkyl moiety or methyl, dimethyl or trimethyl substituted cycloalkyl m
4358617 Substituted tricyclodecane derivatives, processes for producing same and organoleptic uses there November 9, 1982
Described are substituted tricyclodecane derivatives having the generic structure: ##STR1## wherein Y is a moiety having a structure selected from the group consisting of: ##STR2## wherein one of the dashed lines represents a carbon-carbon single bond and the other of the
4346245 Substituted tricyclodecane derivatives August 24, 1982
Described are substituted tricyclodecane derivatives having the generic structure: ##STR1## wherein Y is a moiety having a structure selected from the group consisting of: ##STR2## wherein one of the dashed lines represents a carbon-carbon single bond and the other of the
4337212 Substituted tricyclodecane derivatives, processes for producing same and organoleptic uses there June 29, 1982
Described are substituted tricyclodecane derivatives having the generic structure: ##STR1## wherein Y is a moiety having a structure selected from the group consisting of: ##STR2## wherein one of the dashed lines represents a carbon-carbon single bond and the other of the
4327749 Alkyl esters of 1-alkanoyl cycloalkanols, process for preparing same and organoleptic uses there May 4, 1982
Described is a process for preparing several substituted or unsubstituted cycloalkyl acyl alkanoates defined according to the generic structure: ##STR1## wherein R.sub.1 and R.sub.2 taken together complete a cycloalkyl moiety or methyl, dimethyl or trimethyl substituted cycloalkyl mo
4318863 Substituted tricyclodecane derivatives, processes for producing same and organoleptic uses there March 9, 1982
Described are substituted tricyclodecane derivatives having the generic structure: ##STR1## wherein Y is a moiety having a structure selected from the group consisting of: ##STR2## wherein one of the dashed lines represents a carbon-carbon single bond and the other of the
4310701 Process for the preparation of homologues of methyl dihydrojasmonate January 12, 1982
A process is described for the preparation of alkyl and alkylene homologues of methyl dihydrojasmonatewhich incorporate the novel process step: ##STR1## In the above reaction sequence, X is chloro or bromo and R is C.sub.1 -C.sub.4 alkyl.
4301184 Flavoring with 5-methyl-3,5-octadien-2-one November 17, 1981
Described is a process for augmenting or enhancing the aroma or taste of foodstuffs comprising adding to a foodstuff an aroma or taste augmenting or enhancing quantity of 5-methyl-3,5-octadien-2-one produced according to the process of reacting 2-methyl-2-pentenal with acetone in the pre
4294266 Benzodioxanones and organoleptic uses thereof October 13, 1981
Described are the bicyclic compounds having the generic structure: ##STR1## wherein Z is benzo or cyclohexano and processes for preparing same and compositions containing same for use in augmenting or enhancing the aroma and/or taste of foodstuffs, chewing gums, toothpastes and medic
4289145 Use of acyl trimethyl cyclohexene derivatives in augmenting or enhancing the organoleptic proper September 15, 1981
Described is a process for augmenting or enhancing the aroma or taste of a smoking tobacco comprising the step of adding to smoking tobacco an organoleptic property modifying amount of the compound having the structure: ##STR1##
4284654 Use of 1-hydroxy-1-ethynyl-2,2,6-trimethyl cyclohexane in augmenting or enhancing the aroma or t August 18, 1981
Described is the use of the compound having the structure: ##STR1## for augmenting or enhancing the aroma or taste of a foodstuff.
4278569 2,2,3-Trimethyl-3-cyclopenten-1-ylalkyl, alkenyl and alkylidene, cyclohexanols, organo-leptic us July 14, 1981
Described are perfume and fragrance compositions and perfumed articles including soaps, detergents, powders as well as colognes containing 2,2,3-trimethyl-3-cyclopenten-1-ylalkyl, alkenyl and alkylidene, cyclohexanois, having the generic structure: ##STR1## wherein at least one o
4275251 Substituted tricyclodecane derivatives, processes for producing same and organoleptic uses there June 23, 1981
Described are substituted tricyclodecane derivatives having the generic structure: ##STR1## wherein Y is a moiety having a structure selected from the group consisting of: ##STR2## wherein one of the dashed lines represents a carbon-carbon single bond and the other of the
4265836 Process for producing cis-pent-2-enyl-1-chloride May 5, 1981
A process is described for the preparation of cis-pent-2-enyl-1-chloride according to the reaction: ##STR1##
4264456 Benzodioxanones and organoleptic uses thereof April 28, 1981
Described are the bicyclic compounds having the generic structure: ##STR1## wherein Z is benzo or cyclohexano and processes for preparing same and compositions containing same for use in augmenting or enhancing the aroma and/or taste of foodstuffs, chewing gums, toothpastes and medic
4260830 Process for the preparation of methyl dihydrojasmonate and lower alkyl homologues April 7, 1981
A process described for the preparation of methyl dihydrojasmonate and lower alkyl homologues according to one of the reaction sequences: ##STR1## The first of the above reaction schemes also incorporates the novel process step: ##STR2## In the above reaction sequence, X is c
4260527 Use of 1-acetyl-22,6-trimethyl cyclohexene-1 in augmenting or enhancing the aroma of perfumes an April 7, 1981
Described is a process for preparing .beta.-damascone starting with 2,6,6-trimethyl cyclohex-2-enone and its use in augmenting or enhancing the perfume and cologne.
4259214 Benzodioxanones and organoleptic uses thereof March 31, 1981
Described are the bicyclic compounds having the generic structure: ##STR1## wherein Z is benzo or cyclohexano and processes for preparing same and compositions containing same for use in augmenting or enhancing the aroma and/or taste of foodstuffs, chewing gums, toothpastes and medic
4255275 Benzodioxanones and organoleptic uses thereof March 10, 1981
Described is a process for augmenting or enhancing the aroma of a solid or liquid anionic, cationic or nonionic detergent comprising the step of intimately admixing with said solid and liquid anionic, cationic or nonionic detergent base at least one cyclic chemical compound having the
4250332 Process for preparing acyl trimethyl cyclohexene derivatives and use of intermediates therefor i February 10, 1981
Described is a process for preparing .beta.-damascone starting with 2,6,6-trimethyl cyclohex-2-enone according to the reaction sequence: ##STR1## wherein Z is hydrogen, MgX', Li, Na or K; Y is MgX', Li, Na or K; X' is Cl, Br or I; R is C.sub.1 -C.sub.3 lower alkyl such as methyl, eth
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