JPH0288540A - 液晶性４―（３’―ｎ―アルキルシクロペンチル）カルボン酸エステル - Google Patents
液晶性４―（３’―ｎ―アルキルシクロペンチル）カルボン酸エステルInfo
- Publication number
- JPH0288540A JPH0288540A JP17820389A JP17820389A JPH0288540A JP H0288540 A JPH0288540 A JP H0288540A JP 17820389 A JP17820389 A JP 17820389A JP 17820389 A JP17820389 A JP 17820389A JP H0288540 A JPH0288540 A JP H0288540A
- Authority
- JP
- Japan
- Prior art keywords
- formulas
- tables
- mathematical
- chemical
- chemical formulas
- 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
- 239000007788 liquid Substances 0.000 title claims description 8
- 150000001733 carboxylic acid esters Chemical class 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims abstract description 32
- 239000000126 substance Substances 0.000 claims abstract description 24
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 3
- 229910052794 bromium Inorganic materials 0.000 claims abstract 2
- 229910052801 chlorine Inorganic materials 0.000 claims abstract 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol group Chemical group [C@@H]1(CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)[C@H](C)CCCC(C)C HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims abstract 2
- 150000001875 compounds Chemical class 0.000 claims description 13
- 125000003262 carboxylic acid ester group Chemical class [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims 1
- 239000004973 liquid crystal related substance Substances 0.000 abstract description 9
- 150000002148 esters Chemical class 0.000 abstract description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract description 6
- 239000000463 material Substances 0.000 abstract description 6
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract description 4
- 238000000034 method Methods 0.000 abstract description 4
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 239000012071 phase Substances 0.000 description 10
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 230000007704 transition Effects 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000005684 electric field Effects 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000004988 Nematic liquid crystal Substances 0.000 description 2
- 239000004990 Smectic liquid crystal Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 229940125898 compound 5 Drugs 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- CBYVEGZNJIEUJD-UHFFFAOYSA-N (4-butoxyphenyl) 4-hexoxybenzoate Chemical compound C1=CC(OCCCCCC)=CC=C1C(=O)OC1=CC=C(OCCCC)C=C1 CBYVEGZNJIEUJD-UHFFFAOYSA-N 0.000 description 1
- DFHWCSVHLVOKND-UHFFFAOYSA-N (4-butoxyphenyl) 4-hexylbenzoate Chemical compound C1=CC(CCCCCC)=CC=C1C(=O)OC1=CC=C(OCCCC)C=C1 DFHWCSVHLVOKND-UHFFFAOYSA-N 0.000 description 1
- DHOWBGIVOJLNCG-UHFFFAOYSA-N (4-hexoxyphenyl) 2-methoxybenzoate Chemical compound C(CCCCC)OC1=CC=C(C=C1)OC(C1=C(C=CC=C1)OC)=O DHOWBGIVOJLNCG-UHFFFAOYSA-N 0.000 description 1
- ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 description 1
- MNAQZWYVBSMCRU-UHFFFAOYSA-N 4-(3-butylcyclopentyl)benzoyl chloride Chemical compound C(CCC)C1CC(CC1)C1=CC=C(C(=O)Cl)C=C1 MNAQZWYVBSMCRU-UHFFFAOYSA-N 0.000 description 1
- CVNOWLNNPYYEOH-UHFFFAOYSA-N 4-cyanophenol Chemical compound OC1=CC=C(C#N)C=C1 CVNOWLNNPYYEOH-UHFFFAOYSA-N 0.000 description 1
- OZPPUPJQRJYTNY-UHFFFAOYSA-N 4-pentoxybenzoic acid Chemical compound CCCCCOC1=CC=C(C(O)=O)C=C1 OZPPUPJQRJYTNY-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- LNUFLCYMSVYYNW-ZPJMAFJPSA-N [(2r,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[[(3s,5s,8r,9s,10s,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-disulfo Chemical compound O([C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1C[C@@H]2CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)[C@H]1O[C@H](COS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@H](OS(O)(=O)=O)[C@H]1OS(O)(=O)=O LNUFLCYMSVYYNW-ZPJMAFJPSA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 229940126142 compound 16 Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- LSUIEOBBDXBMCZ-NDENLUEZSA-N methyl 2-[(z)-(9-hydroxy-10-methoxy-2,2,4-trimethyl-1h-chromeno[3,4-f]quinolin-5-ylidene)methyl]thiophene-3-carboxylate Chemical compound C1=CSC(\C=C/2C3=C4C(C)=CC(C)(C)NC4=CC=C3C3=C(OC)C(O)=CC=C3O\2)=C1C(=O)OC LSUIEOBBDXBMCZ-NDENLUEZSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000005693 optoelectronics Effects 0.000 description 1
- 210000004681 ovum Anatomy 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Liquid Crystal Substances (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DD09K/317878-1 | 1988-07-13 | ||
| DD31787988A DD274042B5 (de) | 1988-07-13 | 1988-07-13 | Fluessig-kristalline mischungen |
| DD09K/317879-8 | 1988-07-13 | ||
| DD31787888A DD274041B5 (de) | 1988-07-13 | 1988-07-13 | Fluessig-kristalline mischungen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0288540A true JPH0288540A (ja) | 1990-03-28 |
Family
ID=25748220
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17820389A Pending JPH0288540A (ja) | 1988-07-13 | 1989-07-12 | 液晶性４―（３’―ｎ―アルキルシクロペンチル）カルボン酸エステル |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JPH0288540A (de) |
| CH (1) | CH678858A5 (de) |
| DE (1) | DE3918884A1 (de) |
| GB (1) | GB2220658B (de) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011207785A (ja) * | 2010-03-29 | 2011-10-20 | Sagami Chemical Research Institute | ４−シクロペンチルシクロヘキサノン誘導体及びその製造方法 |
| JP2012001502A (ja) * | 2010-06-18 | 2012-01-05 | Jnc Corp | ５員環を有する化合物、液晶組成物および液晶表示素子 |
| CN102746852A (zh) * | 2012-06-19 | 2012-10-24 | 深圳市华星光电技术有限公司 | 具有五元环的液晶分子 |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09227422A (ja) * | 1996-02-12 | 1997-09-02 | Rolic Ag | シクロペンチル誘導体 |
| GB2310669B (en) * | 1996-02-27 | 2000-09-27 | Merck Patent Gmbh | An electrooptical liquid crystal display of the IPS type containing a liquid crystalline medium having positive dielectric anisotropy and such a medium |
| EP0821049B1 (de) * | 1996-07-26 | 2001-01-10 | Rolic AG | Cyclopentyl-Verbindungen |
| US5759443A (en) * | 1996-07-26 | 1998-06-02 | Rolic Ag | Cyclopentyl derivatives |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3739588A1 (de) * | 1986-12-20 | 1988-07-28 | Merck Patent Gmbh | Cyclopentanabkoemmlinge |
-
1989
- 1989-06-09 DE DE19893918884 patent/DE3918884A1/de not_active Withdrawn
- 1989-06-13 CH CH221189A patent/CH678858A5/de not_active IP Right Cessation
- 1989-07-12 JP JP17820389A patent/JPH0288540A/ja active Pending
- 1989-07-12 GB GB8915950A patent/GB2220658B/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011207785A (ja) * | 2010-03-29 | 2011-10-20 | Sagami Chemical Research Institute | ４−シクロペンチルシクロヘキサノン誘導体及びその製造方法 |
| JP2012001502A (ja) * | 2010-06-18 | 2012-01-05 | Jnc Corp | ５員環を有する化合物、液晶組成物および液晶表示素子 |
| CN102746852A (zh) * | 2012-06-19 | 2012-10-24 | 深圳市华星光电技术有限公司 | 具有五元环的液晶分子 |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2220658A (en) | 1990-01-17 |
| CH678858A5 (de) | 1991-11-15 |
| GB8915950D0 (en) | 1989-08-31 |
| GB2220658B (en) | 1992-04-08 |
| DE3918884A1 (de) | 1990-01-18 |
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