JPS6025973A - ピリミジン類 - Google Patents
ピリミジン類Info
- Publication number
- JPS6025973A JPS6025973A JP13249783A JP13249783A JPS6025973A JP S6025973 A JPS6025973 A JP S6025973A JP 13249783 A JP13249783 A JP 13249783A JP 13249783 A JP13249783 A JP 13249783A JP S6025973 A JPS6025973 A JP S6025973A
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- compound
- formula
- tetraaza
- terphenyl
- 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
- -1 Pyrimidine compound Chemical class 0.000 title abstract description 5
- 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 25
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 abstract description 27
- 239000000463 material Substances 0.000 abstract description 7
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 abstract description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract description 2
- 235000010290 biphenyl Nutrition 0.000 abstract description 2
- 239000004305 biphenyl Substances 0.000 abstract description 2
- 239000003054 catalyst Substances 0.000 abstract description 2
- 239000007789 gas Substances 0.000 abstract description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000007704 transition Effects 0.000 description 3
- 239000012071 phase Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- OXPDQFOKSZYEMJ-UHFFFAOYSA-N 2-phenylpyrimidine Chemical compound C1=CC=CC=C1C1=NC=CC=N1 OXPDQFOKSZYEMJ-UHFFFAOYSA-N 0.000 description 1
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical class C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- LZCZIHQBSCVGRD-UHFFFAOYSA-N benzenecarboximidamide;hydron;chloride Chemical compound [Cl-].NC(=[NH2+])C1=CC=CC=C1 LZCZIHQBSCVGRD-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical compound C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- JABYJIQOLGWMQW-UHFFFAOYSA-N undec-4-ene Chemical compound CCCCCCC=CCCC JABYJIQOLGWMQW-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Liquid Crystal Substances (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13249783A JPS6025973A (ja) | 1983-07-20 | 1983-07-20 | ピリミジン類 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13249783A JPS6025973A (ja) | 1983-07-20 | 1983-07-20 | ピリミジン類 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6025973A true JPS6025973A (ja) | 1985-02-08 |
| JPH0368866B2 JPH0368866B2 (en, 2012) | 1991-10-30 |
Family
ID=15082750
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13249783A Granted JPS6025973A (ja) | 1983-07-20 | 1983-07-20 | ピリミジン類 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6025973A (en, 2012) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4609485A (en) * | 1984-02-17 | 1986-09-02 | Chisso Corporation | Bipyrimidinyl derivatives |
| US4640796A (en) * | 1984-12-27 | 1987-02-03 | Chisso Corporation | 1,4-dipyrimidinylbenzene derivative |
| US4715984A (en) * | 1985-01-22 | 1987-12-29 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Liquid-crystalline dihydroazines |
| JPS63278992A (ja) * | 1987-05-12 | 1988-11-16 | Fujitsu Ltd | 相転移型液晶組成物 |
| US5948551A (en) * | 1994-07-01 | 1999-09-07 | Hoechst Aktiengesellschaft | Use of conjugated compounds containing pyrimidine groups as electroluminescence materials |
| JP2010509781A (ja) * | 2006-11-14 | 2010-03-25 | オスラム オプト セミコンダクターズ ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規の高導電性の有機電荷キャリア輸送材料 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU746497B2 (en) | 1997-08-20 | 2002-05-02 | University Of Miami | A high quality, continuous throughput, tissue fixation-dehydration-fat removal-impregnation method |
-
1983
- 1983-07-20 JP JP13249783A patent/JPS6025973A/ja active Granted
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4609485A (en) * | 1984-02-17 | 1986-09-02 | Chisso Corporation | Bipyrimidinyl derivatives |
| US4640796A (en) * | 1984-12-27 | 1987-02-03 | Chisso Corporation | 1,4-dipyrimidinylbenzene derivative |
| US4715984A (en) * | 1985-01-22 | 1987-12-29 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Liquid-crystalline dihydroazines |
| JPS63278992A (ja) * | 1987-05-12 | 1988-11-16 | Fujitsu Ltd | 相転移型液晶組成物 |
| US5948551A (en) * | 1994-07-01 | 1999-09-07 | Hoechst Aktiengesellschaft | Use of conjugated compounds containing pyrimidine groups as electroluminescence materials |
| JP2010509781A (ja) * | 2006-11-14 | 2010-03-25 | オスラム オプト セミコンダクターズ ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規の高導電性の有機電荷キャリア輸送材料 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0368866B2 (en, 2012) | 1991-10-30 |
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