DE3323127C2 - Phenylderivate von 2,4-Dimethyl-2-hexen und deren Verwendung - Google Patents
Phenylderivate von 2,4-Dimethyl-2-hexen und deren VerwendungInfo
- Publication number
- DE3323127C2 DE3323127C2 DE3323127A DE3323127A DE3323127C2 DE 3323127 C2 DE3323127 C2 DE 3323127C2 DE 3323127 A DE3323127 A DE 3323127A DE 3323127 A DE3323127 A DE 3323127A DE 3323127 C2 DE3323127 C2 DE 3323127C2
- Authority
- DE
- Germany
- Prior art keywords
- dimethyl
- hexene
- low
- methylphenyl
- phenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 title claims abstract description 6
- 239000003205 fragrance Substances 0.000 claims abstract description 16
- 150000001875 compounds Chemical class 0.000 claims abstract description 14
- 239000001257 hydrogen Substances 0.000 claims abstract description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 6
- 239000002304 perfume Substances 0.000 abstract description 6
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 239000000543 intermediate Substances 0.000 abstract description 2
- 238000003786 synthesis reaction Methods 0.000 abstract description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 16
- 239000000126 substance Substances 0.000 description 16
- 239000012044 organic layer Substances 0.000 description 14
- 238000009835 boiling Methods 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- 239000000243 solution Substances 0.000 description 11
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 10
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 10
- 239000000460 chlorine Substances 0.000 description 10
- 229910052801 chlorine Inorganic materials 0.000 description 10
- 235000019645 odor Nutrition 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000012300 argon atmosphere Substances 0.000 description 9
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 8
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 8
- 235000017557 sodium bicarbonate Nutrition 0.000 description 8
- QSYKYIPKHNKFRS-UHFFFAOYSA-N (1-chloro-3,5-dimethylhex-4-enyl)benzene Chemical compound CC(C)=CC(C)CC(Cl)C1=CC=CC=C1 QSYKYIPKHNKFRS-UHFFFAOYSA-N 0.000 description 6
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 6
- YZOPWNASQGPFJR-UHFFFAOYSA-N 2-chlorohex-2-ene Chemical class CCCC=C(C)Cl YZOPWNASQGPFJR-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 5
- 239000004202 carbamide Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- YKYKAXPAICLTGT-UHFFFAOYSA-N 3,5-dimethyl-1-(3-methylphenyl)hex-4-en-1-ol Chemical compound CC(CC(O)C1=CC(=CC=C1)C)C=C(C)C YKYKAXPAICLTGT-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 4
- UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 4
- XZLHIOXQQDQYKT-UHFFFAOYSA-N 1-(1-chloro-3,5-dimethylhex-4-enyl)-3-methylbenzene Chemical compound CC(C)=CC(C)CC(Cl)C1=CC=CC(C)=C1 XZLHIOXQQDQYKT-UHFFFAOYSA-N 0.000 description 3
- HPJXNCBHXIVQEQ-UHFFFAOYSA-N 1-(1-chloro-3,5-dimethylhex-4-enyl)-4-methylbenzene Chemical compound CC(C)=CC(C)CC(Cl)C1=CC=C(C)C=C1 HPJXNCBHXIVQEQ-UHFFFAOYSA-N 0.000 description 3
- BYNCCOCJFJXXQZ-UHFFFAOYSA-N 3,5-dimethyl-1-(4-methylphenyl)hex-4-en-1-ol Chemical compound CC(CC(O)C1=CC=C(C=C1)C)C=C(C)C BYNCCOCJFJXXQZ-UHFFFAOYSA-N 0.000 description 3
- SVWRCUQEKBNBLN-UHFFFAOYSA-N 3,5-dimethyl-1-phenylhex-4-en-1-ol Chemical compound CC(CC(O)C1=CC=CC=C1)C=C(C)C SVWRCUQEKBNBLN-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000005457 ice water Substances 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 230000002085 persistent effect Effects 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000011592 zinc chloride Substances 0.000 description 3
- 235000005074 zinc chloride Nutrition 0.000 description 3
- RCJMVGJKROQDCB-UHFFFAOYSA-N 2-methylpenta-1,3-diene Chemical group CC=CC(C)=C RCJMVGJKROQDCB-UHFFFAOYSA-N 0.000 description 2
- REGIUFZVMMENCC-UHFFFAOYSA-N 3,5-dimethyl-1-(3-methylphenyl)hex-4-en-1-one Chemical compound CC(C)=CC(C)CC(=O)C1=CC=CC(C)=C1 REGIUFZVMMENCC-UHFFFAOYSA-N 0.000 description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
- CJSBUWDGPXGFGA-UHFFFAOYSA-N 4-methylpenta-1,3-diene Chemical compound CC(C)=CC=C CJSBUWDGPXGFGA-UHFFFAOYSA-N 0.000 description 2
- 240000000662 Anethum graveolens Species 0.000 description 2
- 241000167854 Bourreria succulenta Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 244000179970 Monarda didyma Species 0.000 description 2
- 235000010672 Monarda didyma Nutrition 0.000 description 2
- 235000009754 Vitis X bourquina Nutrition 0.000 description 2
- 235000012333 Vitis X labruscana Nutrition 0.000 description 2
- 240000006365 Vitis vinifera Species 0.000 description 2
- 235000014787 Vitis vinifera Nutrition 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 235000019693 cherries Nutrition 0.000 description 2
- -1 cologne Substances 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000001724 (4,8-dimethyl-2-propan-2-ylidene-3,3a,4,5,6,8a-hexahydro-1H-azulen-6-yl) acetate Substances 0.000 description 1
- JZHGRUMIRATHIU-UHFFFAOYSA-N 1-ethenyl-3-methylbenzene Chemical compound CC1=CC=CC(C=C)=C1 JZHGRUMIRATHIU-UHFFFAOYSA-N 0.000 description 1
- AFQYGZFERFQKQG-UHFFFAOYSA-N 3,5-dimethyl-1-(4-methylphenyl)hex-4-en-1-one Chemical compound CC(C)=CC(C)CC(=O)C1=CC=C(C)C=C1 AFQYGZFERFQKQG-UHFFFAOYSA-N 0.000 description 1
- DHZXQNALSASBEO-UHFFFAOYSA-N 3,5-dimethyl-1-phenylhex-4-en-1-one Chemical compound CC(C)=CC(C)CC(=O)C1=CC=CC=C1 DHZXQNALSASBEO-UHFFFAOYSA-N 0.000 description 1
- ZLYGXQYHWPEHHX-UHFFFAOYSA-N 3-methyl-1-phenylhex-4-en-1-one Chemical class CC=CC(C)CC(=O)C1=CC=CC=C1 ZLYGXQYHWPEHHX-UHFFFAOYSA-N 0.000 description 1
- JIGUICYYOYEXFS-UHFFFAOYSA-N 3-tert-butylbenzene-1,2-diol Chemical compound CC(C)(C)C1=CC=CC(O)=C1O JIGUICYYOYEXFS-UHFFFAOYSA-N 0.000 description 1
- 244000144725 Amygdalus communis Species 0.000 description 1
- 235000011437 Amygdalus communis Nutrition 0.000 description 1
- 241000208152 Geranium Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- UAVFEMBKDRODDE-UHFFFAOYSA-N Vetiveryl acetate Chemical compound CC1CC(OC(C)=O)C=C(C)C2CC(=C(C)C)CC12 UAVFEMBKDRODDE-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 235000020224 almond Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000008365 aromatic ketones Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 235000021384 green leafy vegetables Nutrition 0.000 description 1
- 239000003845 household chemical Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0061—Essential oils; Perfumes compounds containing a six-membered aromatic ring not condensed with another ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/272—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions
- C07C17/275—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of hydrocarbons and halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C22/00—Cyclic compounds containing halogen atoms bound to an acyclic carbon atom
- C07C22/02—Cyclic compounds containing halogen atoms bound to an acyclic carbon atom having unsaturation in the rings
- C07C22/04—Cyclic compounds containing halogen atoms bound to an acyclic carbon atom having unsaturation in the rings containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C33/00—Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C33/28—Alcohols containing only six-membered aromatic rings as cyclic part with unsaturation outside the aromatic rings
- C07C33/30—Alcohols containing only six-membered aromatic rings as cyclic part with unsaturation outside the aromatic rings monocyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/29—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/29—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
- C07C45/292—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups with chromium derivatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/794—Ketones containing a keto group bound to a six-membered aromatic ring having unsaturation outside an aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3323127A DE3323127C2 (de) | 1983-06-27 | 1983-06-27 | Phenylderivate von 2,4-Dimethyl-2-hexen und deren Verwendung |
NL8302289A NL8302289A (nl) | 1983-06-27 | 1983-06-28 | Fenylderivaten van 2,4-dimethyl-2-hexeen. |
GB08318557A GB2163148B (en) | 1983-06-27 | 1983-07-08 | Phenyl derivatives of 2,4-dimethyl-2-hexene |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3323127A DE3323127C2 (de) | 1983-06-27 | 1983-06-27 | Phenylderivate von 2,4-Dimethyl-2-hexen und deren Verwendung |
NL8302289A NL8302289A (nl) | 1983-06-27 | 1983-06-28 | Fenylderivaten van 2,4-dimethyl-2-hexeen. |
GB08318557A GB2163148B (en) | 1983-06-27 | 1983-07-08 | Phenyl derivatives of 2,4-dimethyl-2-hexene |
Publications (2)
Publication Number | Publication Date |
---|---|
DE3323127A1 DE3323127A1 (de) | 1985-01-03 |
DE3323127C2 true DE3323127C2 (de) | 1987-01-22 |
Family
ID=27191092
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE3323127A Expired DE3323127C2 (de) | 1983-06-27 | 1983-06-27 | Phenylderivate von 2,4-Dimethyl-2-hexen und deren Verwendung |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE3323127C2 (fr) |
GB (1) | GB2163148B (fr) |
NL (1) | NL8302289A (fr) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL88674A0 (en) * | 1987-12-18 | 1989-07-31 | Norwich Eaton Pharma | Preparation of certain substituted aromatic compounds |
-
1983
- 1983-06-27 DE DE3323127A patent/DE3323127C2/de not_active Expired
- 1983-06-28 NL NL8302289A patent/NL8302289A/nl not_active Application Discontinuation
- 1983-07-08 GB GB08318557A patent/GB2163148B/en not_active Expired
Non-Patent Citations (1)
Title |
---|
NICHTS-ERMITTELT |
Also Published As
Publication number | Publication date |
---|---|
GB2163148B (en) | 1987-04-23 |
NL8302289A (nl) | 1985-01-16 |
GB2163148A (en) | 1986-02-19 |
DE3323127A1 (de) | 1985-01-03 |
GB8318557D0 (en) | 1983-08-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0341707B1 (fr) | Ester phényléthylique de l'acide ortho-cinnamique, sa préparation et son utilisation comme agent parfumant | |
CH617349A5 (fr) | ||
EP0177807B1 (fr) | Hexanoates, procédé de leur préparation et parfums et/ou agents aromatiques ayant une teneur en tels composés | |
CH600882A5 (fr) | ||
DE60009394T2 (de) | Cyclopentylalkylnitrile und die Verwendung von Cyclopentylalkyl-Derivaten als Duftstoffe | |
EP0086945B1 (fr) | Alcénols, procédé de leur préparation, utilisation de ceux-ci à titre de parfums et compositions odoriférantes contenant ces alcénols | |
DE3323127C2 (de) | Phenylderivate von 2,4-Dimethyl-2-hexen und deren Verwendung | |
EP0301375A2 (fr) | Aldéhydes bicycliques | |
EP0045453A1 (fr) | Alcénols (I) et leur procédé de synthèse, utilisation de (I) comme agent parfumant et/ou aromatisant ainsi que les compositions parfumantes et/ou aromatisantes contenant (I) | |
EP0045861B1 (fr) | Composés insaturés, leur procédé de préparation, leur utilisation comme parfums ainsi que les compositions parfumantes les contenant | |
EP0191365B1 (fr) | Oximes araliphatiques, procédé pour leur préparation et compositions odoriférantes contenant de tels composés | |
DE2359659C3 (de) | 4-Tricyclo [5.2.1.02·6! decyl-8-butanal, Verfahren zu seiner Herstellung und Verwendung als Riechstoff | |
EP0115007B1 (fr) | Acides alcoxy-acétiques, leur procédé de préparation et leur utilisation | |
DE3108868C2 (de) | Exo- und/oder Endo-tricyclo[5.2.1.0↑2↑↑,↑↑6↑]decan-2-carbonsäureester, Verfahren zu ihrer Herstellung und sie enthaltende Duftstoffzusammensetzungen | |
DE2644762C2 (de) | Verwendung von 2-Äthyl-6,6-dimethyl-2-cyclohexen-1-carbonsäureäthylester als Riechstoff | |
DE2733857A1 (de) | Verfahren zur herstellung von riechstoffen und riechstoffkompositionen | |
DE1811289C3 (de) | cis-1,7,7-Trimethyl-bicyclo eckige Klammer auf 4,4,0 eckige Klammer zu decanon- (3), Verfahren zu dessen Herstellung und dessen Verwendung als Riechstoff | |
AT382611B (de) | Verfahren zur herstellung neuer 2,4-dimethyl-2 -hexenderivate | |
DE2517620A1 (de) | Verwendung von exo-norbornyl-2- essigsaeureestern als riechstoffe sowie diese enthaltende riechstoffkompositionen | |
AT377697B (de) | Riechstoffkomposition | |
CH654565A5 (en) | Phenyl derivatives of 2,4-dimethyl-2-hexene | |
EP0098791A1 (fr) | Esters de l'acide 2-méthylpentanoique avec alcools ramifiés ou carbocycliques, leur préparation et leur utilisation comme produits odoriférants | |
DE2918168A1 (de) | Verwendung von 4,6-dioxa-5-alkyl- tricyclo eckige klammer auf 7.2.1.0 hoch 2,8 eckige klammer zu -dodec-10-enen als riechstoffe, sowie diese enthaltende riechstoffkompositionen | |
DE2639182A1 (de) | 3-(10-undecenyloxy)-propionitril, verfahren zu seiner herstellung und seine verwendung | |
DE2622611A1 (de) | Neue riechstoffgemische |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
8110 | Request for examination paragraph 44 | ||
D2 | Grant after examination | ||
8364 | No opposition during term of opposition | ||
8339 | Ceased/non-payment of the annual fee |