JPS5829745A - トランス−4−置換シクロヘキサンカルボン酸2−ハロゲノ−4−クロロフエニルエステル - Google Patents
トランス−4−置換シクロヘキサンカルボン酸2−ハロゲノ−4−クロロフエニルエステルInfo
- Publication number
- JPS5829745A JPS5829745A JP12690881A JP12690881A JPS5829745A JP S5829745 A JPS5829745 A JP S5829745A JP 12690881 A JP12690881 A JP 12690881A JP 12690881 A JP12690881 A JP 12690881A JP S5829745 A JPS5829745 A JP S5829745A
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- trans
- compound shown
- formulai
- cyclohexanecarboxylic acid
- 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 Trans-4-substituted cyclohexanecarboxylic acid Chemical class 0.000 title claims abstract description 5
- 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 29
- 239000000203 mixture Substances 0.000 claims abstract description 26
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 22
- NZNMSOFKMUBTKW-UHFFFAOYSA-N Cyclohexanecarboxylic acid Natural products OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 abstract description 11
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract description 8
- VZFUCHSFHOYXIS-UHFFFAOYSA-N cycloheptane carboxylic acid Natural products OC(=O)C1CCCCCC1 VZFUCHSFHOYXIS-UHFFFAOYSA-N 0.000 abstract description 7
- 239000004988 Nematic liquid crystal Substances 0.000 abstract description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract description 4
- 238000000034 method Methods 0.000 abstract description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 4
- OQIHEFMTIUJJET-HDRKRICHSA-N CC[C@H]1CC[C@@H](CC1)[C@H]1CC[C@@H](CC1)C(O)=O Chemical class CC[C@H]1CC[C@@H](CC1)[C@H]1CC[C@@H](CC1)C(O)=O OQIHEFMTIUJJET-HDRKRICHSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 3
- 229910001887 tin oxide Inorganic materials 0.000 description 3
- ZKMUKBBWORLNLA-UHFFFAOYSA-N 4-chloro-2-fluorophenol Chemical compound OC1=CC=C(Cl)C=C1F ZKMUKBBWORLNLA-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 2
- 239000004472 Lysine Substances 0.000 description 2
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 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 description 1
- YQYBDBKKLNEINV-UHFFFAOYSA-N 3,4-diphenylbenzonitrile Chemical group C=1C=CC=CC=1C1=CC(C#N)=CC=C1C1=CC=CC=C1 YQYBDBKKLNEINV-UHFFFAOYSA-N 0.000 description 1
- GPGGNNIMKOVSAG-UHFFFAOYSA-N 4-(4-octoxyphenyl)benzonitrile Chemical group C1=CC(OCCCCCCCC)=CC=C1C1=CC=C(C#N)C=C1 GPGGNNIMKOVSAG-UHFFFAOYSA-N 0.000 description 1
- BPMBNLJJRKCCRT-UHFFFAOYSA-N 4-phenylbenzonitrile Chemical group C1=CC(C#N)=CC=C1C1=CC=CC=C1 BPMBNLJJRKCCRT-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
- RVLAXPQGTRTHEV-XYPYZODXSA-N CCCCC[C@H]1CC[C@H](C(O)=O)CC1 Chemical compound CCCCC[C@H]1CC[C@H](C(O)=O)CC1 RVLAXPQGTRTHEV-XYPYZODXSA-N 0.000 description 1
- 239000005973 Carvone Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-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
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 210000002858 crystal cell Anatomy 0.000 description 1
- RVOJTCZRIKWHDX-UHFFFAOYSA-N cyclohexanecarbonyl chloride Chemical compound ClC(=O)C1CCCCC1 RVOJTCZRIKWHDX-UHFFFAOYSA-N 0.000 description 1
- 150000001934 cyclohexanes Chemical class 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
Landscapes
- Liquid Crystal (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Liquid Crystal Substances (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12690881A JPS5829745A (ja) | 1981-08-13 | 1981-08-13 | トランス−4−置換シクロヘキサンカルボン酸2−ハロゲノ−4−クロロフエニルエステル |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12690881A JPS5829745A (ja) | 1981-08-13 | 1981-08-13 | トランス−4−置換シクロヘキサンカルボン酸2−ハロゲノ−4−クロロフエニルエステル |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5829745A true JPS5829745A (ja) | 1983-02-22 |
JPH0210817B2 JPH0210817B2 (en]) | 1990-03-09 |
Family
ID=14946862
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12690881A Granted JPS5829745A (ja) | 1981-08-13 | 1981-08-13 | トランス−4−置換シクロヘキサンカルボン酸2−ハロゲノ−4−クロロフエニルエステル |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5829745A (en]) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0576403A (ja) * | 1991-06-13 | 1993-03-30 | Takashi Kiyohara | 靴の加温中敷 |
JPH05115310A (ja) * | 1991-07-15 | 1993-05-14 | Takashi Kiyohara | 靴の加温中敷 |
-
1981
- 1981-08-13 JP JP12690881A patent/JPS5829745A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH0210817B2 (en]) | 1990-03-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS6251257B2 (en]) | ||
JPS5829745A (ja) | トランス−4−置換シクロヘキサンカルボン酸2−ハロゲノ−4−クロロフエニルエステル | |
JPS5813544A (ja) | トランス−4−置換シクロヘキサンカルボン酸3−クロロ−4−フルオロフエニルエステル | |
JPS58126839A (ja) | 4−(トランス−4′−アルキルシクロヘキシル)安息香酸2,4−ジハロゲノフエニルエステル | |
JPS58118543A (ja) | トランス−4−(4′−置換フエニル)シクロヘキサンカルボン酸2,4−ジハロゲノフエニルエステル | |
JPH0150691B2 (en]) | ||
JPH039895B2 (en]) | ||
JPH0150693B2 (en]) | ||
JPS58121247A (ja) | トランス−4−(4′−置換フエニル)シクロヘキサンカルボン酸3−クロロ−4−ハロゲノフエニルエステル | |
JPS58126838A (ja) | 4−(トランス−4′−アルキルシクロヘキシル)安息香酸3−クロロ−4−ハロゲノフエニルエステル | |
JPS58121272A (ja) | 3−クロロ−6−ヒドロキシピリジンのエステル誘導体 | |
JPS60237048A (ja) | エステル化合物 | |
JPS63303951A (ja) | 光学活性な化合物およびそれを含む液晶組成物 | |
JPH0131499B2 (en]) | ||
JPS5899456A (ja) | トランス−4−(4′−置換フエニル)シアノシクロヘキサン | |
JPS59157057A (ja) | エステル化合物 | |
JPH0232044A (ja) | アルケニルオキシ安息酸ハロゲノビフェニルエステル | |
JPH0247455B2 (ja) | 44arufua*arufua*arufuaatorifuruoromechiruansokukosann44*toransuu4**arukirushikurohekishiru*fueniruesuteru | |
JPH0251893B2 (en]) | ||
JPS584745A (ja) | トランス−4−(4′−置換フエニル)−シクロヘキサンカルボン酸4″−クロロフエニルエステル | |
JPS6168447A (ja) | フエノオキシ酢酸エステル誘導体 | |
JPS59128354A (ja) | シクロヘキサンカルボン酸ハロゲノフエニルエステル誘導体 | |
JPS58210044A (ja) | 4′(トランス−4″−アルキルシクロヘキシル)ビフエニル−4−カルボン酸−2′′′,4′′′−ジハロゲノフエニルエステル | |
JPS6136251A (ja) | 3−ハロゲノ−4−シアノフエノ−ルのエステル誘導体 | |
JPS61282345A (ja) | エステル化合物 |