GB1296581A - - Google Patents
Info
- Publication number
- GB1296581A GB1296581A GB5111370A GB1296581DA GB1296581A GB 1296581 A GB1296581 A GB 1296581A GB 5111370 A GB5111370 A GB 5111370A GB 1296581D A GB1296581D A GB 1296581DA GB 1296581 A GB1296581 A GB 1296581A
- Authority
- GB
- United Kingdom
- Prior art keywords
- para
- diphenyl
- silane
- dimethyl
- tolylaminophenoxy
- 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
- 235000010290 biphenyl Nutrition 0.000 abstract 4
- 239000004305 biphenyl Substances 0.000 abstract 4
- 125000006267 biphenyl group Chemical group 0.000 abstract 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 abstract 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- -1 methylethoxy Chemical group 0.000 abstract 2
- 150000004756 silanes Chemical class 0.000 abstract 2
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 abstract 1
- QSXZBXKVVLHLHB-UHFFFAOYSA-N 4-[(4-anilinophenoxy)-dimethylsilyl]oxy-n-phenylaniline Chemical compound C=1C=C(NC=2C=CC=CC=2)C=CC=1O[Si](C)(C)OC(C=C1)=CC=C1NC1=CC=CC=C1 QSXZBXKVVLHLHB-UHFFFAOYSA-N 0.000 abstract 1
- CRFUTNMZLDHCOM-UHFFFAOYSA-N 4-[(4-anilinophenoxy)-diphenylsilyl]oxy-N-phenylaniline Chemical compound C1(=CC=CC=C1)[Si](OC1=CC=C(C=C1)NC1=CC=CC=C1)(OC1=CC=C(C=C1)NC1=CC=CC=C1)C1=CC=CC=C1 CRFUTNMZLDHCOM-UHFFFAOYSA-N 0.000 abstract 1
- JNRWZPANVZCQJB-UHFFFAOYSA-N 4-[(4-anilinophenoxy)-methyl-phenylsilyl]oxy-N-phenylaniline Chemical compound C[Si](OC1=CC=C(NC2=CC=CC=C2)C=C1)(OC1=CC=C(NC2=CC=CC=C2)C=C1)C1=CC=CC=C1 JNRWZPANVZCQJB-UHFFFAOYSA-N 0.000 abstract 1
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 abstract 1
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003508 Dilauryl thiodipropionate Substances 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- DSPGIFMGZQAIGY-UHFFFAOYSA-N N-[(4-methoxyphenyl)methyl]-2-[[2-[(4-methoxyphenyl)methylamino]phenoxy]-dimethylsilyl]oxyaniline Chemical compound C[Si](OC1=C(C=CC=C1)NCC1=CC=C(C=C1)OC)(OC1=C(C=CC=C1)NCC1=CC=C(C=C1)OC)C DSPGIFMGZQAIGY-UHFFFAOYSA-N 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 235000019270 ammonium chloride Nutrition 0.000 abstract 1
- 239000003963 antioxidant agent Substances 0.000 abstract 1
- 239000006227 byproduct Substances 0.000 abstract 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical class Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 235000019304 dilauryl thiodipropionate Nutrition 0.000 abstract 1
- 239000012760 heat stabilizer Substances 0.000 abstract 1
- 150000003840 hydrochlorides Chemical class 0.000 abstract 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 1
- 239000004611 light stabiliser Substances 0.000 abstract 1
- CXHGCYZTKLYFDS-UHFFFAOYSA-N n-[4-[dimethyl-[4-(naphthalen-2-ylamino)phenoxy]silyl]oxyphenyl]naphthalen-2-amine Chemical compound C1=CC=CC2=CC(NC3=CC=C(C=C3)O[Si](C)(OC=3C=CC(NC=4C=C5C=CC=CC5=CC=4)=CC=3)C)=CC=C21 CXHGCYZTKLYFDS-UHFFFAOYSA-N 0.000 abstract 1
- 125000000109 phenylethoxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])O* 0.000 abstract 1
- 229920000570 polyether Polymers 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 229920000098 polyolefin Polymers 0.000 abstract 1
- 229920006324 polyoxymethylene Polymers 0.000 abstract 1
- 239000002243 precursor Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 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
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5111370 | 1970-10-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1296581A true GB1296581A (enExample) | 1972-11-15 |
Family
ID=10458709
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5111370A Expired GB1296581A (enExample) | 1970-10-28 | 1970-10-28 |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1296581A (enExample) |
-
1970
- 1970-10-28 GB GB5111370A patent/GB1296581A/en not_active Expired
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |