JPS60156682A - ３，４−エポキシ−トリシクロ〔５，２，１，ｏ↑２’↑６〕デカン−８，９−ジカルボン酸 - Google Patents
３，４−エポキシ−トリシクロ〔５，２，１，ｏ↑２’↑６〕デカン−８，９−ジカルボン酸Info
- Publication number
- JPS60156682A JPS60156682A JP1140684A JP1140684A JPS60156682A JP S60156682 A JPS60156682 A JP S60156682A JP 1140684 A JP1140684 A JP 1140684A JP 1140684 A JP1140684 A JP 1140684A JP S60156682 A JPS60156682 A JP S60156682A
- Authority
- JP
- Japan
- Prior art keywords
- epoxy
- formula
- tricyclo
- dicarboxylic acid
- decane
- 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.)
- Granted
Links
- FBZANWBJFUBGEF-UHFFFAOYSA-N 4-oxatetracyclo[6.2.1.02,7.03,5]undecane-9,10-dicarboxylic acid Chemical compound C12C3OC3CC2C2C(C(=O)O)C(C(O)=O)C1C2 FBZANWBJFUBGEF-UHFFFAOYSA-N 0.000 title 1
- VSIWDRMSJHKGDT-UHFFFAOYSA-N 2-heptyl-3-methylbutanedioic acid Chemical compound CCCCCCCC(C(O)=O)C(C)C(O)=O VSIWDRMSJHKGDT-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 11
- 150000001875 compounds Chemical class 0.000 abstract description 8
- 230000003647 oxidation Effects 0.000 abstract description 5
- 238000007254 oxidation reaction Methods 0.000 abstract description 5
- 238000006243 chemical reaction Methods 0.000 abstract description 4
- 125000003700 epoxy group Chemical group 0.000 abstract description 4
- 150000001451 organic peroxides Chemical class 0.000 abstract description 4
- 229920000642 polymer Polymers 0.000 abstract description 4
- 239000004593 Epoxy Substances 0.000 abstract description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 3
- 239000000178 monomer Substances 0.000 abstract description 3
- 239000004645 polyester resin Substances 0.000 abstract description 3
- 229920001225 polyester resin Polymers 0.000 abstract description 3
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- 238000004132 cross linking Methods 0.000 abstract description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 abstract description 2
- 239000003814 drug Substances 0.000 abstract description 2
- 238000002360 preparation method Methods 0.000 abstract 2
- 239000003905 agrochemical Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003822 epoxy resin Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 229920000647 polyepoxide Polymers 0.000 abstract 1
- 239000002994 raw material Substances 0.000 abstract 1
- 230000009257 reactivity Effects 0.000 abstract 1
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 6
- 239000013078 crystal Substances 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- XYPISWUKQGWYGX-UHFFFAOYSA-N 2,2,2-trifluoroethaneperoxoic acid Chemical compound OOC(=O)C(F)(F)F XYPISWUKQGWYGX-UHFFFAOYSA-N 0.000 description 1
- LJGHYPLBDBRCRZ-UHFFFAOYSA-N 3-(3-aminophenyl)sulfonylaniline Chemical compound NC1=CC=CC(S(=O)(=O)C=2C=C(N)C=CC=2)=C1 LJGHYPLBDBRCRZ-UHFFFAOYSA-N 0.000 description 1
- YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
- 101000797623 Homo sapiens Protein AMBP Proteins 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 1
- 102100032859 Protein AMBP Human genes 0.000 description 1
- 241000405961 Scomberomorus regalis Species 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000001460 carbon-13 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 108700039708 galantide Proteins 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- LULAYUGMBFYYEX-UHFFFAOYSA-N metachloroperbenzoic acid Natural products OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Epoxy Compounds (AREA)
- Polyesters Or Polycarbonates (AREA)
- Epoxy Resins (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1140684A JPS60156682A (ja) | 1984-01-25 | 1984-01-25 | ３，４−エポキシ−トリシクロ〔５，２，１，ｏ↑２’↑６〕デカン−８，９−ジカルボン酸 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1140684A JPS60156682A (ja) | 1984-01-25 | 1984-01-25 | ３，４−エポキシ−トリシクロ〔５，２，１，ｏ↑２’↑６〕デカン−８，９−ジカルボン酸 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60156682A true JPS60156682A (ja) | 1985-08-16 |
| JPH0517227B2 JPH0517227B2 (https=) | 1993-03-08 |
Family
ID=11777135
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1140684A Granted JPS60156682A (ja) | 1984-01-25 | 1984-01-25 | ３，４−エポキシ−トリシクロ〔５，２，１，ｏ↑２’↑６〕デカン−８，９−ジカルボン酸 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60156682A (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001328959A (ja) * | 2000-05-19 | 2001-11-27 | Nissan Chem Ind Ltd | アクリレート化合物及びその製造法 |
| US20140066590A1 (en) * | 2011-04-28 | 2014-03-06 | Nissan Chemical Industries, Ltd. | Polyimide precursor modified with dicarboxylic acid anhydride, imidized polyimide and liquid crystal aligning agent using it |
-
1984
- 1984-01-25 JP JP1140684A patent/JPS60156682A/ja active Granted
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001328959A (ja) * | 2000-05-19 | 2001-11-27 | Nissan Chem Ind Ltd | アクリレート化合物及びその製造法 |
| US20140066590A1 (en) * | 2011-04-28 | 2014-03-06 | Nissan Chemical Industries, Ltd. | Polyimide precursor modified with dicarboxylic acid anhydride, imidized polyimide and liquid crystal aligning agent using it |
| US9447240B2 (en) * | 2011-04-28 | 2016-09-20 | Nissan Chemical Industries, Ltd. | Polyimide precursor modified with dicarboxylic acid anhydride, imidized polyimide and liquid crystal aligning agent using it |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0517227B2 (https=) | 1993-03-08 |
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