JPS6361292B2 - - Google Patents
Info
- Publication number
- JPS6361292B2 JPS6361292B2 JP12907081A JP12907081A JPS6361292B2 JP S6361292 B2 JPS6361292 B2 JP S6361292B2 JP 12907081 A JP12907081 A JP 12907081A JP 12907081 A JP12907081 A JP 12907081A JP S6361292 B2 JPS6361292 B2 JP S6361292B2
- Authority
- JP
- Japan
- Prior art keywords
- trans
- liquid crystal
- cyclohexylbenzene
- alkylcyclohexyl
- propylcyclohexyl
- 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
- HHNHBFLGXIUXCM-GFCCVEGCSA-N cyclohexylbenzene Chemical compound [CH]1CCCC[C@@H]1C1=CC=CC=C1 HHNHBFLGXIUXCM-GFCCVEGCSA-N 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000004973 liquid crystal related substance Substances 0.000 description 19
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 3
- 229910000343 potassium bisulfate Inorganic materials 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229910000564 Raney nickel Inorganic materials 0.000 description 2
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- ANRQGKOBLBYXFM-UHFFFAOYSA-M phenylmagnesium bromide Chemical compound Br[Mg]C1=CC=CC=C1 ANRQGKOBLBYXFM-UHFFFAOYSA-M 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- XXUSEPRYHRDKFV-CTYIDZIISA-N C1C[C@@H](CCC)CC[C@@H]1C1=CC=C(C#N)C=C1 Chemical compound C1C[C@@H](CCC)CC[C@@H]1C1=CC=C(C#N)C=C1 XXUSEPRYHRDKFV-CTYIDZIISA-N 0.000 description 1
- FURZYCFZFBYJBT-JCNLHEQBSA-N C1C[C@@H](CCCCC)CC[C@@H]1C1=CC=C(C#N)C=C1 Chemical compound C1C[C@@H](CCCCC)CC[C@@H]1C1=CC=C(C#N)C=C1 FURZYCFZFBYJBT-JCNLHEQBSA-N 0.000 description 1
- FRKVGIKPQJABFV-QSPIWVMWSA-N CCC[C@H]1CC[C@@H](CC1)C1CCCCC1=O Chemical compound CCC[C@H]1CC[C@@H](CC1)C1CCCCC1=O FRKVGIKPQJABFV-QSPIWVMWSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000010531 catalytic reduction reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- -1 pentylcyclohexyl Chemical group 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Liquid Crystal Substances (AREA)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12907081A JPS5832832A (ja) | 1981-08-18 | 1981-08-18 | トランス―4’―(トランス―4”―アルキルシクロヘキシル)シクロヘキシルベンゼン |
US06/358,794 US4422951A (en) | 1981-04-02 | 1982-03-16 | Liquid crystal benzene derivatives |
EP82301631A EP0062470B1 (en) | 1981-04-02 | 1982-03-29 | Liquid crystal benzene derivatives |
DE8282301631T DE3260570D1 (en) | 1981-04-02 | 1982-03-29 | Liquid crystal benzene derivatives |
HK440/89A HK44089A (en) | 1981-04-02 | 1989-05-25 | Liquid crystal benzene derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12907081A JPS5832832A (ja) | 1981-08-18 | 1981-08-18 | トランス―4’―(トランス―4”―アルキルシクロヘキシル)シクロヘキシルベンゼン |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5832832A JPS5832832A (ja) | 1983-02-25 |
JPS6361292B2 true JPS6361292B2 (en]) | 1988-11-28 |
Family
ID=15000331
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12907081A Granted JPS5832832A (ja) | 1981-04-02 | 1981-08-18 | トランス―4’―(トランス―4”―アルキルシクロヘキシル)シクロヘキシルベンゼン |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5832832A (en]) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3211601A1 (de) * | 1982-03-30 | 1983-10-06 | Merck Patent Gmbh | Hydroterphenyle |
US4599654A (en) * | 1984-10-31 | 1986-07-08 | Rca Corporation | Dark current eliminator useful for auto-iris controller |
US5485144A (en) * | 1993-05-07 | 1996-01-16 | Pittway Corporation | Compensated ionization sensor |
-
1981
- 1981-08-18 JP JP12907081A patent/JPS5832832A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5832832A (ja) | 1983-02-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0062470B1 (en) | Liquid crystal benzene derivatives | |
JPS6239136B2 (en]) | ||
JPS64373B2 (en]) | ||
JPS6344132B2 (en]) | ||
JPS6313411B2 (en]) | ||
JPS644497B2 (en]) | ||
JPS6361292B2 (en]) | ||
JPS5916840A (ja) | 3−フルオロ−4−置換−〔トランス−4′−(トランス−4″−アルキルシクロヘキシル)シクロヘキシル〕ベンゼン | |
JPH0359050B2 (en]) | ||
JPS6353177B2 (en]) | ||
JPS6332051B2 (en]) | ||
JPS64942B2 (en]) | ||
JPH0229055B2 (ja) | Jishikurohekishirubenzenjudotai | |
JPS5916834A (ja) | 2,4↓−ジメチル↓−1↓−〔トランス↓−4′↓−(トランス↓−4″↓−アルキルシクロヘキシル)シクロヘキシル〕ベンゼン | |
JPS6360011B2 (en]) | ||
JPH0212455B2 (en]) | ||
JPS64372B2 (en]) | ||
JPH0150212B2 (en]) | ||
JPS6348252B2 (en]) | ||
JPH0222742B2 (en]) | ||
JPH0139408B2 (en]) | ||
JPH0158168B2 (en]) | ||
JPH0237333B2 (en]) | ||
JPH0220615B2 (en]) | ||
JPH0212454B2 (en]) |