JP2011213837A5 - - Google Patents
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- Publication number
- JP2011213837A5 JP2011213837A5 JP2010082492A JP2010082492A JP2011213837A5 JP 2011213837 A5 JP2011213837 A5 JP 2011213837A5 JP 2010082492 A JP2010082492 A JP 2010082492A JP 2010082492 A JP2010082492 A JP 2010082492A JP 2011213837 A5 JP2011213837 A5 JP 2011213837A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- general formula
- fluorine
- hydrogen atom
- 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
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- 150000001875 compounds Chemical class 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 11
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 11
- 229910052731 fluorine Inorganic materials 0.000 claims description 11
- 239000011737 fluorine Substances 0.000 claims description 11
- 229920000570 polyether Polymers 0.000 claims description 11
- -1 dicarboxylic acid fluoride compound Chemical class 0.000 claims description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 125000005499 phosphonyl group Chemical group 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- YGHMOOKDWGSWJI-UHFFFAOYSA-N Cc(cc1)ccc1OC(F)=C(F)F Chemical compound Cc(cc1)ccc1OC(F)=C(F)F YGHMOOKDWGSWJI-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 101100388055 Mus musculus Polm gene Proteins 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 2
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- PGFXOWRDDHCDTE-UHFFFAOYSA-N hexafluoropropylene oxide Chemical compound FC(F)(F)C1(F)OC1(F)F PGFXOWRDDHCDTE-UHFFFAOYSA-N 0.000 description 2
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 description 2
- ZQXCQTAELHSNAT-UHFFFAOYSA-N 1-chloro-3-nitro-5-(trifluoromethyl)benzene Chemical compound [O-][N+](=O)C1=CC(Cl)=CC(C(F)(F)F)=C1 ZQXCQTAELHSNAT-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 0 CC(C(Oc1ccc(*)cc1)F)(F)F Chemical compound CC(C(Oc1ccc(*)cc1)F)(F)F 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 239000004811 fluoropolymer Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000007966 viscous suspension Substances 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010082492A JP2011213837A (ja) | 2010-03-31 | 2010-03-31 | 含フッ素ポリエーテル化合物、その製造方法およびそれを含有する硬化性組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010082492A JP2011213837A (ja) | 2010-03-31 | 2010-03-31 | 含フッ素ポリエーテル化合物、その製造方法およびそれを含有する硬化性組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2011213837A JP2011213837A (ja) | 2011-10-27 |
| JP2011213837A5 true JP2011213837A5 (enExample) | 2012-09-06 |
Family
ID=44943918
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010082492A Pending JP2011213837A (ja) | 2010-03-31 | 2010-03-31 | 含フッ素ポリエーテル化合物、その製造方法およびそれを含有する硬化性組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2011213837A (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5757189B2 (ja) * | 2011-08-03 | 2015-07-29 | ユニマテック株式会社 | 熱硬化性含フッ素ポリエーテル化合物およびその製造方法 |
| JP6194957B2 (ja) | 2013-08-09 | 2017-09-13 | ユニマテック株式会社 | ビス（パーフルオロエーテルカルボン酸アルキル）アミノエステルおよびその製造法 |
| CN107207410A (zh) | 2015-02-03 | 2017-09-26 | 优迈特株式会社 | 含氟醚单羧酸氨基烷基酯及其制造方法 |
| TW202334277A (zh) * | 2021-12-14 | 2023-09-01 | 日商信越化學工業股份有限公司 | 含氟活性能量線硬化性組成物、硬化物以及物品 |
| JP7861798B2 (ja) * | 2021-12-14 | 2026-05-19 | 信越化学工業株式会社 | フルオロポリエーテル基含有アクリル化合物 |
-
2010
- 2010-03-31 JP JP2010082492A patent/JP2011213837A/ja active Pending
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