JPS6157835B2 - - Google Patents
Info
- Publication number
- JPS6157835B2 JPS6157835B2 JP55147333A JP14733380A JPS6157835B2 JP S6157835 B2 JPS6157835 B2 JP S6157835B2 JP 55147333 A JP55147333 A JP 55147333A JP 14733380 A JP14733380 A JP 14733380A JP S6157835 B2 JPS6157835 B2 JP S6157835B2
- Authority
- JP
- Japan
- Prior art keywords
- compound represented
- group
- compound
- reaction
- molecular 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.)
- Expired
Links
- 150000001875 compounds Chemical class 0.000 claims description 34
- 229920001021 polysulfide Polymers 0.000 claims description 16
- 239000005077 polysulfide Substances 0.000 claims description 16
- 150000008117 polysulfides Polymers 0.000 claims description 16
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- -1 silane compound Chemical class 0.000 description 26
- 238000006243 chemical reaction Methods 0.000 description 12
- 239000007788 liquid Substances 0.000 description 11
- 238000005259 measurement Methods 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 229910000077 silane Inorganic materials 0.000 description 9
- 239000003960 organic solvent Substances 0.000 description 7
- 238000007259 addition reaction Methods 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- 238000000921 elemental analysis Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- KYVBNYUBXIEUFW-UHFFFAOYSA-N 1,1,3,3-tetramethylguanidine Chemical compound CN(C)C(=N)N(C)C KYVBNYUBXIEUFW-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- ZRALSGWEFCBTJO-UHFFFAOYSA-N anhydrous guanidine Natural products NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 239000012772 electrical insulation material Substances 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical class [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55147333A JPS5770895A (en) | 1980-10-21 | 1980-10-21 | Silicon-modified polysulfide compound |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55147333A JPS5770895A (en) | 1980-10-21 | 1980-10-21 | Silicon-modified polysulfide compound |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5770895A JPS5770895A (en) | 1982-05-01 |
| JPS6157835B2 true JPS6157835B2 (enExample) | 1986-12-09 |
Family
ID=15427803
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55147333A Granted JPS5770895A (en) | 1980-10-21 | 1980-10-21 | Silicon-modified polysulfide compound |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5770895A (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2813469C (en) * | 2010-10-06 | 2016-01-12 | Novartis Ag | Polymerizable chain-extended polysiloxanes with pendant hydrophilic groups |
| TW202424059A (zh) * | 2022-09-12 | 2024-06-16 | 日商力森諾科股份有限公司 | 樹脂材料及樹脂組成物 |
-
1980
- 1980-10-21 JP JP55147333A patent/JPS5770895A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5770895A (en) | 1982-05-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4323488A (en) | Method for the preparation of silicone-modified polyoxyalkylene polyethers and room temperature-curable compositions therewith | |
| US5354880A (en) | Cyclic silylureas and process of preparation | |
| JP2000103794A (ja) | 含硫黄有機珪素化合物の製造方法およびその合成中間体の製造方法 | |
| US6759545B2 (en) | Organosilicon compounds and preparation processes | |
| JPS609759B2 (ja) | ヒドロアルケニルオキシシラン | |
| JPS6340194B2 (enExample) | ||
| EP0098911B1 (en) | Improved process for the preparation of oximatohydridosilanes and aminoxyhydridosilanes | |
| JPS6157835B2 (enExample) | ||
| JPS6017799B2 (ja) | 有機けい素化合物 | |
| JP2016204287A (ja) | 加水分解性シリル基含有環状オルガノハイドロジェンシロキサン | |
| JPS59524B2 (ja) | シリコ−ン変性ポリオキシアルキレンの製造方法 | |
| JPS6257657B2 (enExample) | ||
| JPH09165393A (ja) | 有機けい素化合物及びその製造方法 | |
| JPS6017798B2 (ja) | 有機けい素化合物 | |
| JPH0366695A (ja) | 含フッ素カルボン酸誘導体及びその製造方法 | |
| GB2027440A (en) | Monoamido short chain siloxanes | |
| JPH04252228A (ja) | シリコーン含有エポキシ化合物及びその製法 | |
| JP2850726B2 (ja) | 有機ケイ素化合物及びその製造方法 | |
| EP0395434B1 (en) | Organosilicon compound | |
| JPH0662853B2 (ja) | 室温硬化性オルガノポリシロキサン組成物 | |
| JPH0717752B2 (ja) | アルコキシ官能性オルガノポリシロキサンの製造方法 | |
| JPH085903B2 (ja) | エポキシ基含有アルコキシシロキサン及びその製造方法 | |
| EP0395433B1 (en) | Organosilicon compound | |
| JPH0649204A (ja) | ポリオキサゾリン変性シランおよびその製造方法 | |
| JPH06166690A (ja) | 含フッ素有機ケイ素化合物 |