JP2000063681A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2000063681A5 JP2000063681A5 JP1998238239A JP23823998A JP2000063681A5 JP 2000063681 A5 JP2000063681 A5 JP 2000063681A5 JP 1998238239 A JP1998238239 A JP 1998238239A JP 23823998 A JP23823998 A JP 23823998A JP 2000063681 A5 JP2000063681 A5 JP 2000063681A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- examples
- exemplified
- alkyl
- above 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
- 125000000217 alkyl group Chemical group 0.000 description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 12
- -1 heptylene group Chemical group 0.000 description 11
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 10
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 7
- 125000003545 alkoxy group Chemical group 0.000 description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 5
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 4
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical group CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 3
- 125000002252 acyl group Chemical group 0.000 description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 3
- 125000003277 amino group Chemical class 0.000 description 2
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 2
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 2
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
- HXLAEGYMDGUSBD-UHFFFAOYSA-N 3-[diethoxy(methyl)silyl]propan-1-amine Chemical compound CCO[Si](C)(OCC)CCCN HXLAEGYMDGUSBD-UHFFFAOYSA-N 0.000 description 1
- ZYAASQNKCWTPKI-UHFFFAOYSA-N 3-[dimethoxy(methyl)silyl]propan-1-amine Chemical compound CO[Si](C)(OC)CCCN ZYAASQNKCWTPKI-UHFFFAOYSA-N 0.000 description 1
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- WHGNXNCOTZPEEK-UHFFFAOYSA-N dimethoxy-methyl-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](C)(OC)CCCOCC1CO1 WHGNXNCOTZPEEK-UHFFFAOYSA-N 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10238239A JP2000063681A (ja) | 1998-08-25 | 1998-08-25 | 電気・電子用硬化性有機樹脂組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10238239A JP2000063681A (ja) | 1998-08-25 | 1998-08-25 | 電気・電子用硬化性有機樹脂組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000063681A JP2000063681A (ja) | 2000-02-29 |
| JP2000063681A5 true JP2000063681A5 (enExample) | 2005-10-27 |
Family
ID=17027223
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10238239A Pending JP2000063681A (ja) | 1998-08-25 | 1998-08-25 | 電気・電子用硬化性有機樹脂組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2000063681A (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4755330B2 (ja) * | 2000-09-26 | 2011-08-24 | 東レ・ダウコーニング株式会社 | オルガノポリシロキサン、およびその製造方法 |
| US12215226B2 (en) | 2018-10-30 | 2025-02-04 | Dow Toray Co., Ltd. | Curable reactive silicone composition, cured product thereof and uses of composition and cured product |
| JP7513365B2 (ja) | 2018-12-27 | 2024-07-09 | ダウ・東レ株式会社 | 硬化性シリコーン組成物、その硬化物、およびその製造方法 |
| US12172357B2 (en) | 2018-12-27 | 2024-12-24 | Dow Toray Co., Ltd. | Method for producing curable silicone sheet having hot melt properties |
| WO2020138409A1 (ja) | 2018-12-27 | 2020-07-02 | ダウ・東レ株式会社 | 硬化性シリコーン組成物、その硬化物、およびその製造方法 |
| WO2020203304A1 (ja) | 2019-03-29 | 2020-10-08 | ダウ・東レ株式会社 | 硬化性シリコーン組成物、その硬化物、およびその製造方法 |
| EP3950844A4 (en) | 2019-03-29 | 2022-12-21 | Dow Toray Co., Ltd. | CURABLE SILICONE COMPOSITION, CURED PRODUCT THEREOF AND METHOD OF MAKING THEREOF |
| WO2020203305A1 (ja) | 2019-03-29 | 2020-10-08 | ダウ・東レ株式会社 | 硬化性シリコーン組成物、その硬化物、およびその製造方法 |
| JP2021107550A (ja) | 2019-12-27 | 2021-07-29 | ダウ・東レ株式会社 | 硬化性ホットメルトシリコーン組成物、その硬化物、及び前記組成物又は硬化物を含む積層体 |
-
1998
- 1998-08-25 JP JP10238239A patent/JP2000063681A/ja active Pending
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP3831481B2 (ja) | カルバシラトラン誘導体、その製造方法、接着促進剤、および硬化性シリコーン組成物 | |
| US5614640A (en) | Epoxy functional siloxanes | |
| JP4270593B2 (ja) | 分岐状シロキサン・シルアルキレン共重合体 | |
| JPH06172536A (ja) | 室温硬化性シリコーンシーラント及びその製造方法 | |
| JPH0753919A (ja) | 常温硬化性組成物 | |
| JP2000063681A5 (enExample) | ||
| JPH0517489A (ja) | シロキサン化合物 | |
| US4536265A (en) | Siloxane polyphotoinitiators of the substituted acetophenone type | |
| JP6105616B2 (ja) | 加水分解性シラン | |
| JP4012680B2 (ja) | 有機ケイ素化合物 | |
| EP3666781A1 (en) | Organosilicon compound and thermosetting heat conductive silicone composition | |
| EP0908462B1 (en) | Silatrane derivative and curable silicone composition containing same | |
| JPH11158379A (ja) | 接着促進剤および硬化性シリコーン組成物 | |
| EP1600450B1 (en) | Silane compound having at least two protected functional groups and method for preparing the same | |
| JP4148544B2 (ja) | シラトラン誘導体およびその製造方法 | |
| US20120264964A1 (en) | Alkoxysilane compounds having fluoroalkyl group and method of preparing the same | |
| JP3865082B2 (ja) | シロキサン化合物およびその製造方法 | |
| US6365643B1 (en) | Photoinitiators for cationic curing | |
| US9862735B2 (en) | Organosilicon compound having diphenylethyl and methoxysilyl and making method | |
| US5239085A (en) | Organocyclosiloxane and method for its preparation | |
| JPH10330386A (ja) | 有機シリル基及びカルバメート結合含有アルコキシシラン化合物 | |
| US10683312B2 (en) | Glycoluril ring-containing organosilicon compound and making method | |
| JP3924055B2 (ja) | シラトラン誘導体およびその製造方法 | |
| EP1714968A1 (en) | Protected piperazino group-bearing organoxysilane compound and making method | |
| JP2002097273A5 (enExample) |