DE2353146A1 - Neue riechstoffe - Google Patents
Neue riechstoffeInfo
- Publication number
- DE2353146A1 DE2353146A1 DE19732353146 DE2353146A DE2353146A1 DE 2353146 A1 DE2353146 A1 DE 2353146A1 DE 19732353146 DE19732353146 DE 19732353146 DE 2353146 A DE2353146 A DE 2353146A DE 2353146 A1 DE2353146 A1 DE 2353146A1
- Authority
- DE
- Germany
- Prior art keywords
- pentenyl
- methyl
- cyclopentene
- oxo
- formula
- 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.)
- Pending
Links
- 239000003205 fragrance Substances 0.000 title claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 14
- -1 3-Isopropyl-1-ethyl-2- (3-oxo-4-pentenyl) -1-cyclopentene Chemical compound 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- MPXTWSIOPUFAIC-UHFFFAOYSA-N 4-methyl-5-(2-methyl-5-propan-2-ylcyclopenten-1-yl)pent-1-en-3-one Chemical compound CC(C)C1CCC(C)=C1CC(C)C(=O)C=C MPXTWSIOPUFAIC-UHFFFAOYSA-N 0.000 claims description 2
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 229910052739 hydrogen Inorganic materials 0.000 claims 5
- 239000001257 hydrogen Substances 0.000 claims 5
- 239000002253 acid Substances 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 4
- 241000218645 Cedrus Species 0.000 description 3
- 239000003810 Jones reagent Substances 0.000 description 3
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 3
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000005770 Eugenol Substances 0.000 description 2
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- HQKQRXZEXPXXIG-VJOHVRBBSA-N chembl2333940 Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@H]1[C@@](OC(C)=O)(C)CC2 HQKQRXZEXPXXIG-VJOHVRBBSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
- 229960002217 eugenol Drugs 0.000 description 2
- 239000011981 lindlar catalyst Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 1
- ZXSQEZNORDWBGZ-UHFFFAOYSA-N 1,3-dihydropyrrolo[2,3-b]pyridin-2-one Chemical compound C1=CN=C2NC(=O)CC2=C1 ZXSQEZNORDWBGZ-UHFFFAOYSA-N 0.000 description 1
- YWXISZCPWGECJB-UHFFFAOYSA-N 2,4-dimethyl-5-(2-methyl-5-prop-1-en-2-ylcyclopenten-1-yl)pent-1-en-3-ol Chemical compound CC(=C)C(O)C(C)CC1=C(C)CCC1C(C)=C YWXISZCPWGECJB-UHFFFAOYSA-N 0.000 description 1
- LYMGADGLKNZGHW-UHFFFAOYSA-N 2,4-dimethyl-5-(2-methyl-5-propan-2-ylcyclopenten-1-yl)pent-1-en-3-ol Chemical compound CC(C)C1CCC(C)=C1CC(C)C(O)C(C)=C LYMGADGLKNZGHW-UHFFFAOYSA-N 0.000 description 1
- VXARGJXXRJQLGT-UHFFFAOYSA-N 2-methyl-5-(2-methyl-5-propan-2-ylcyclopenten-1-yl)pent-1-en-3-ol Chemical compound CC(C)C1CCC(C)=C1CCC(O)C(C)=C VXARGJXXRJQLGT-UHFFFAOYSA-N 0.000 description 1
- FQKXENOGAUAKMO-UHFFFAOYSA-N 2-methyl-5-(2-methyl-5-propan-2-ylcyclopenten-1-yl)pent-1-en-3-one Chemical compound CC(C)C1CCC(C)=C1CCC(=O)C(C)=C FQKXENOGAUAKMO-UHFFFAOYSA-N 0.000 description 1
- GETUAIWURIZCFQ-UHFFFAOYSA-N 4-methyl-5-(2-methyl-5-propan-2-ylcyclopenten-1-yl)pent-1-en-3-ol Chemical compound CC(C)C1CCC(C)=C1CC(C)C(O)C=C GETUAIWURIZCFQ-UHFFFAOYSA-N 0.000 description 1
- MTTXVKINIZZXON-UHFFFAOYSA-N 5-(2-methyl-5-propan-2-ylcyclopenten-1-yl)pent-1-en-3-ol Chemical compound CC(C)C1CCC(C)=C1CCC(O)C=C MTTXVKINIZZXON-UHFFFAOYSA-N 0.000 description 1
- PTJAYXBJKLZTQH-UHFFFAOYSA-N 5-(2-methyl-5-propan-2-ylcyclopenten-1-yl)pent-1-en-3-one Chemical compound CC(C)C1CCC(C)=C1CCC(=O)C=C PTJAYXBJKLZTQH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000402754 Erythranthe moschata Species 0.000 description 1
- 235000019501 Lemon oil Nutrition 0.000 description 1
- GLZPCOQZEFWAFX-JXMROGBWSA-N Nerol Natural products CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 description 1
- 235000019502 Orange oil Nutrition 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- GOPYZMJAIPBUGX-UHFFFAOYSA-N [O-2].[O-2].[Mn+4] Chemical class [O-2].[O-2].[Mn+4] GOPYZMJAIPBUGX-UHFFFAOYSA-N 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 235000001053 badasse Nutrition 0.000 description 1
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 235000000484 citronellol Nutrition 0.000 description 1
- 239000001926 citrus aurantium l. subsp. bergamia wright et arn. oil Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- VWWMOACCGFHMEV-UHFFFAOYSA-N dicarbide(2-) Chemical compound [C-]#[C-] VWWMOACCGFHMEV-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 1
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 244000056931 lavandin Species 0.000 description 1
- 235000009606 lavandin Nutrition 0.000 description 1
- 239000000171 lavandula angustifolia l. flower oil Substances 0.000 description 1
- 239000010501 lemon oil Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000010671 sandalwood oil Substances 0.000 description 1
- LKZMBDSASOBTPN-UHFFFAOYSA-L silver carbonate Substances [Ag].[O-]C([O-])=O LKZMBDSASOBTPN-UHFFFAOYSA-L 0.000 description 1
- 229910001958 silver carbonate Inorganic materials 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000271 synthetic detergent Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000010678 thyme oil Substances 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
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
- C11B9/003—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing less than six carbon atoms
-
- 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
- C07C49/20—Unsaturated compounds containing keto groups bound to acyclic carbon atoms
- C07C49/21—Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing rings other than six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1660572A CH573381A5 (US07909888-20110322-C00008.png) | 1972-11-15 | 1972-11-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2353146A1 true DE2353146A1 (de) | 1974-05-22 |
Family
ID=4418716
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19732353146 Pending DE2353146A1 (de) | 1972-11-15 | 1973-10-23 | Neue riechstoffe |
Country Status (7)
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4250061A (en) * | 1979-06-18 | 1981-02-10 | Givaudan Corporation | 2-Acetyl-1,3,3,4,4-pentamethylcyclopentene as a fragrance material |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3285950A (en) * | 1963-10-02 | 1966-11-15 | Hoffmann La Roche | Unsaturated esters of chrysanthemum monocarboxylic acid |
-
1972
- 1972-11-15 CH CH1660572A patent/CH573381A5/xx not_active IP Right Cessation
-
1973
- 1973-10-12 NL NL7314094A patent/NL7314094A/xx not_active Application Discontinuation
- 1973-10-23 DE DE19732353146 patent/DE2353146A1/de active Pending
- 1973-11-07 US US05/413,470 patent/US3932517A/en not_active Expired - Lifetime
- 1973-11-13 JP JP12764273A patent/JPS5418241B2/ja not_active Expired
- 1973-11-14 GB GB5287873A patent/GB1391749A/en not_active Expired
- 1973-11-15 FR FR7340677A patent/FR2206306B1/fr not_active Expired
-
1978
- 1978-02-03 JP JP1138078A patent/JPS53109958A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| US3932517A (en) | 1976-01-13 |
| JPS53109958A (en) | 1978-09-26 |
| CH573381A5 (US07909888-20110322-C00008.png) | 1976-03-15 |
| NL7314094A (US07909888-20110322-C00008.png) | 1974-05-17 |
| JPS5418241B2 (US07909888-20110322-C00008.png) | 1979-07-06 |
| FR2206306A1 (US07909888-20110322-C00008.png) | 1974-06-07 |
| GB1391749A (en) | 1975-04-23 |
| FR2206306B1 (US07909888-20110322-C00008.png) | 1977-03-11 |
| JPS4980040A (US07909888-20110322-C00008.png) | 1974-08-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0076493B1 (de) | Verwendung von 1,1-Di(C1-C6-alkyl)-2-phenyl-ethan-Derivaten als Riechstoffe | |
| CH622762A5 (US07909888-20110322-C00008.png) | ||
| DE1923223A1 (de) | Derivate des 1-AEthyl-3,3-dimethyl-cyclo-hexans und Verfahren zu deren Herstellung | |
| EP0252378B1 (de) | Neue aliphatische Aldehyde, Verhahren zu deren Herstellung und deren Verwendung als Riechstoffe | |
| WO2011067386A2 (de) | Verfahren zur herstellung von aliphatischen aldehyden | |
| DE2835445C2 (de) | Verwendung von Estern des Gemisches der Tricyclo-[5.2.1.0↑2↑↑.↑↑6↑]decan-3- und Tricyclo [5.2.1.0↑2↑↑.↑↑6↑]decan-4-carbonsäure als Riechstoffe, sowie diese enthaltende Riechstoffkompositionen | |
| EP0002510A1 (de) | Cyclohexane, Verfahren zu deren Herstellung, deren Verwendung und diese enthaltende Kompositionen | |
| EP0086945B1 (de) | Neue Alkenole(I), Verfahren zu deren Herstellung, Verwendung von (I) als Riechstoffe und Riechstoffkompositionen mit einem Gehalt an (I) | |
| DE2756772C2 (US07909888-20110322-C00008.png) | ||
| EP0044413B1 (de) | 3,6-Dimethyl-oct-1-in-3-ole und -oct-1-en-3-ole sowie Derivate davon und ihre Verwendung als Riechstoffe und Verfahren zur Herstellung von 3,6-Dimethyl-octan-3-ol | |
| DE2353146A1 (de) | Neue riechstoffe | |
| DE2925622A1 (de) | 4(5)-acetyl-7,7,9(7,9,9)-trimethylbicyclo eckige klammer auf 4.3.0 eckige klammer zu non-1-en, dessen herstellung und verwendung als riechstoff, sowie dieses enthaltende riechstoffkompositionen | |
| DE2353147A1 (de) | Neue riechstoffe | |
| DE2804075C2 (de) | Substituierte Cyclohexane, Verfahren zu ihrer Herstellung und Riechstoffkompositionen, die solche Verbindungen enthalten | |
| DE2359659B2 (de) | 4-Tricyclo [5A1.02·6! decyl-8-butanal. Verfahren zu seiner Herstellung und Verwendung als Riechstoff | |
| CH580426A5 (en) | (3-Keto-4-pentenyl)-1-cyclopentene perfumes - prepd. by oxidising the 3-hydroxy-4-pentenyl derivs | |
| DE2757559C2 (de) | Verwendung der 3,5,5-Trimethylhexansäureester als Riechstoffe sowie diese enthaltende Riechstoffkompositionen | |
| EP0291849B1 (de) | 4-Methyl-4-phenyl-1-pentanale, deren Herstellung und Verwendung als Riechstoffe | |
| DE2255119C2 (de) | Parfümkomposition | |
| EP0341538B1 (de) | 1-Tert.-Butoxy-omega-alkene und deren Verwendung als Riechstoffe | |
| DE2553328C2 (de) | Verfahren zur Herstellung von Riechstoffzusammensetzungen, parfümierten Stoffen oder parfümierten Artikeln und 8-Allyl-8-hydroxytricyclo [5,2,1,0↑2↑↑,↑↑6↑] decan | |
| DE2252808A1 (de) | Neue riechstoffe | |
| DE2365939B2 (de) | Cyclopentene, Verfahren zu deren Herstellung und Riechstoffkompositionen | |
| EP0315895A1 (de) | Tricyclische Verbindungen | |
| DE10026004A1 (de) | 3,3-Dimethylcyclohexan-Derivate |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OHW | Rejection |