DE2257051A1 - Organosiliciumcinnamate - Google Patents
OrganosiliciumcinnamateInfo
- Publication number
- DE2257051A1 DE2257051A1 DE2257051A DE2257051A DE2257051A1 DE 2257051 A1 DE2257051 A1 DE 2257051A1 DE 2257051 A DE2257051 A DE 2257051A DE 2257051 A DE2257051 A DE 2257051A DE 2257051 A1 DE2257051 A1 DE 2257051A1
- Authority
- DE
- Germany
- Prior art keywords
- mol
- sio
- formula
- free
- radical
- 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
- -1 siloxane units Chemical group 0.000 claims description 24
- 239000004215 Carbon black (E152) Substances 0.000 claims description 12
- 229930195733 hydrocarbon Natural products 0.000 claims description 12
- 229920001577 copolymer Polymers 0.000 claims description 11
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 150000008282 halocarbons Chemical class 0.000 claims 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000005755 formation reaction Methods 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- KCMITHMNVLRGJU-CMDGGOBGSA-N Allyl cinnamate Chemical compound C=CCOC(=O)\C=C\C1=CC=CC=C1 KCMITHMNVLRGJU-CMDGGOBGSA-N 0.000 description 2
- WBYWAXJHAXSJNI-UHFFFAOYSA-N cinnamic acid Chemical class OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 150000002148 esters Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 150000004756 silanes Chemical class 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical group [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 2
- IJOOHPMOJXWVHK-UHFFFAOYSA-N trimethylsilyl-trifluoromethansulfonate Natural products C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 2
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
- IKYAJDOSWUATPI-UHFFFAOYSA-N 3-[dimethoxy(methyl)silyl]propane-1-thiol Chemical compound CO[Si](C)(OC)CCCS IKYAJDOSWUATPI-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 101150065749 Churc1 gene Proteins 0.000 description 1
- 102100038239 Protein Churchill Human genes 0.000 description 1
- 229910003923 SiC 4 Inorganic materials 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 241001293891 Zosime Species 0.000 description 1
- 230000009102 absorption Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000002344 aminooxy group Chemical group [H]N([H])O[*] 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229940114081 cinnamate Drugs 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- JJQZDUKDJDQPMQ-UHFFFAOYSA-N dimethoxy(dimethyl)silane Chemical compound CO[Si](C)(C)OC JJQZDUKDJDQPMQ-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000005826 halohydrocarbons Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- TXDNPSYEJHXKMK-UHFFFAOYSA-N sulfanylsilane Chemical class S[SiH3] TXDNPSYEJHXKMK-UHFFFAOYSA-N 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/12—Organo silicon halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
- C07F7/0892—Compounds with a Si-O-N linkage
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
- C08G77/392—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing sulfur
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Silicon Polymers (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20118871A | 1971-11-22 | 1971-11-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2257051A1 true DE2257051A1 (de) | 1973-05-30 |
Family
ID=22744837
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2257051A Pending DE2257051A1 (de) | 1971-11-22 | 1972-11-21 | Organosiliciumcinnamate |
Country Status (7)
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3884860A (en) * | 1974-04-15 | 1975-05-20 | Dow Corning | Carboxy-functional silicones |
| JPS59206465A (ja) * | 1983-05-10 | 1984-11-22 | Shin Etsu Chem Co Ltd | 放射線硬化性オルガノポリシロキサン組成物 |
| US4665147A (en) * | 1983-06-30 | 1987-05-12 | Loctite Corporation | Novel methacrylated siloxanes |
| GB8322317D0 (en) * | 1983-08-18 | 1983-09-21 | Dow Corning Ltd | Organosilicon compounds |
| US4562278A (en) * | 1984-10-12 | 1985-12-31 | Dow Corning, Ltd. | Organosilicon compounds and preparation and use thereof |
| US5412133A (en) * | 1987-07-31 | 1995-05-02 | General Electric Company | Radiation active silicon compounds having thioether linked functional groups |
| FR2634769B1 (fr) * | 1988-07-29 | 1990-10-05 | Rhone Poulenc Chimie | Diorganopolysiloxane a fonction thioalkylacrylate |
| US4985565A (en) * | 1989-10-16 | 1991-01-15 | Dow Corning Corporation | Silacyclobutanes |
| US5486633A (en) * | 1994-11-10 | 1996-01-23 | Duke University | Photochemically-removable silyl protecting groups |
| KR0179115B1 (ko) * | 1995-11-20 | 1999-05-01 | 구자홍 | 액정배향용 감광성물질 및 이를 이용한 액정표시장치 |
| BR112017006015B1 (pt) * | 2014-09-23 | 2021-09-14 | Momentive Performance Materials Gmbh | Poliorganossiloxano, método para tratar substratos à base de aminoácido, composição para tratar substratos à base de aminoácido, e kit |
-
0
- BE BE791682D patent/BE791682A/xx unknown
-
1971
- 1971-11-22 US US00201188A patent/US3767690A/en not_active Expired - Lifetime
-
1972
- 1972-08-01 CA CA148,409A patent/CA973191A/en not_active Expired
- 1972-09-27 JP JP9695972A patent/JPS568038B2/ja not_active Expired
- 1972-11-21 FR FR7241262A patent/FR2160896B1/fr not_active Expired
- 1972-11-21 DE DE2257051A patent/DE2257051A1/de active Pending
- 1972-11-22 GB GB5401272A patent/GB1373458A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS568038B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1981-02-20 |
| FR2160896B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1975-11-07 |
| GB1373458A (en) | 1974-11-13 |
| FR2160896A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1973-07-06 |
| US3767690A (en) | 1973-10-23 |
| BE791682A (fr) | 1973-05-21 |
| CA973191A (en) | 1975-08-19 |
| JPS4857932A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1973-08-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0396130B1 (de) | Alkenyloxyfunktionelle Organosiliciumverbindungen, deren Herstellung und Verwendung | |
| DE69306698T2 (de) | Polydiorganosiloxan mit Alkoxyendgruppen und von diesem abgeleitete, bei Umgebungstemperatur vulkanisierbare Siliconelastomere | |
| DE1262271B (de) | Verfahren zur Herstellung von Organosiliciumverbindungen | |
| DE2918254C2 (de) | Verfahren zur Herstellung von vernetzten Organopolysiloxanen und deren Verwendung in abhäsiven Beschichtungsmassen | |
| EP0000929B1 (de) | Zu Elastomeren vernetzende Massen auf Basis von Polysiloxanen | |
| DE2335118B2 (de) | Acrylat- oder substituierte Acrylatgruppen enthaltende Organopolysiloxane und Verfahren zu ihrer Herstellung | |
| DE3106186A1 (de) | Verfahren zur herstellung von organopolysiloxanen und verwendung dieser organop | |
| DE2257051A1 (de) | Organosiliciumcinnamate | |
| DE1244781B (de) | Verfahren zur Herstellung von Mercaptoalkylaminoalkylsilanen | |
| DE69118140T2 (de) | Hitze-härtbare Einkomponenten-Polysiloxanzusammensetzung | |
| DE4002879A1 (de) | Alkenylgruppen aufweisende siloxancopolymere, deren herstellung und verwendung | |
| DE19612086A1 (de) | Verfahren zum Einführen von funktionellen Gruppen in Organosiloxan-Kondensationsprodukte | |
| EP0168645A2 (de) | Perfluoralkylnorbornylsilane oder -siloxane, deren Herstellung und Verwendung | |
| DE1668637A1 (de) | Neue Organosiliciumverbindungen mit Esterfunktionen | |
| DE19957336A1 (de) | Vernetzbare Organopolysiloxanmassen | |
| EP0401684B1 (de) | Verfahren zur Herstellung von Organosiloxanen | |
| EP0690062B1 (de) | Furanylgruppen aufweisende Organosiliciumverbindungen | |
| DE1595543A1 (de) | Neue oel- und loesungsmittelbestaendige harzartige Fluorkohlenwasserstoffpolysiloxane und Verfahren zu deren Herstellung | |
| DE4108334A1 (de) | Alkenylgruppen aufweisende organosiliciumverbindungen, verfahren zu ihrer herstellung und verwendung dieser organosiliciumverbindungen | |
| US3576028A (en) | Polyalkoxysilanes | |
| DE19654556A1 (de) | Harnstoffgruppen aufweisende Organosiliciumverbindungen, deren Herstellung sowie deren Verwendung | |
| DE2409383A1 (de) | Schwefelhaltige perfluoralkylsiliciumverbindungen | |
| DE2415669A1 (de) | Fluoralkylthiomethylsilane und verfahren zu ihrer herstellung | |
| DE60120147T2 (de) | Härtbare silikonharz-zusammensetzung und reaktive siliziumverbindungen | |
| DE2811854A1 (de) | Verfahren zur herstellung von silanen |