CH626914A5 - - Google Patents
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- Publication number
- CH626914A5 CH626914A5 CH286177A CH286177A CH626914A5 CH 626914 A5 CH626914 A5 CH 626914A5 CH 286177 A CH286177 A CH 286177A CH 286177 A CH286177 A CH 286177A CH 626914 A5 CH626914 A5 CH 626914A5
- Authority
- CH
- Switzerland
- Prior art keywords
- formula
- radical
- rings
- alkyl
- denotes
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 39
- 239000000203 mixture Substances 0.000 claims description 25
- -1 nitro- Chemical class 0.000 claims description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 125000003545 alkoxy group Chemical group 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 125000001424 substituent group Chemical group 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 125000002560 nitrile group Chemical group 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 239000004973 liquid crystal related substance Substances 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims description 3
- 125000002252 acyl group Chemical group 0.000 claims 2
- 125000005157 alkyl carboxy group Chemical group 0.000 claims 2
- 125000001246 bromo group Chemical group Br* 0.000 claims 2
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- 150000002825 nitriles Chemical class 0.000 claims 1
- 239000005871 repellent Substances 0.000 claims 1
- 239000000654 additive Substances 0.000 description 7
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 6
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 230000005669 field effect Effects 0.000 description 3
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- OCBFFGCSTGGPSQ-UHFFFAOYSA-N [CH2]CC Chemical compound [CH2]CC OCBFFGCSTGGPSQ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000004423 acyloxy group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- WPWHSFAFEBZWBB-UHFFFAOYSA-N 1-butyl radical Chemical compound [CH2]CCC WPWHSFAFEBZWBB-UHFFFAOYSA-N 0.000 description 1
- 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
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 239000004988 Nematic liquid crystal Substances 0.000 description 1
- 239000002262 Schiff base Substances 0.000 description 1
- 150000004753 Schiff bases Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 description 1
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 230000002631 hypothermal effect Effects 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
-
- 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
- C09K19/10—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
- C09K19/22—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and nitrogen atoms as chain links, e.g. Schiff bases
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Liquid Crystal Substances (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH286177A CH626914A5 (pl) | 1977-03-08 | 1977-03-08 | |
| DE19772716610 DE2716610A1 (de) | 1977-03-08 | 1977-04-15 | Fluessigkristalline verbindungen |
| AT429477A AT350123B (de) | 1977-03-08 | 1977-06-17 | Fluessigkristallmischung |
| US05/882,742 US4167489A (en) | 1977-03-08 | 1978-03-02 | Liquid crystalline compounds |
| GB8780/78A GB1601317A (en) | 1977-03-08 | 1978-03-06 | Aromatic schiffs bases and their use in liquid crystalline compounds |
| JP2645578A JPS53112832A (en) | 1977-03-08 | 1978-03-08 | New liquid crystal compound * method of its production * mixture * intermediate compound and method for production of this intermediate compound |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH286177A CH626914A5 (pl) | 1977-03-08 | 1977-03-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH626914A5 true CH626914A5 (pl) | 1981-12-15 |
Family
ID=4243226
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH286177A CH626914A5 (pl) | 1977-03-08 | 1977-03-08 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4167489A (pl) |
| JP (1) | JPS53112832A (pl) |
| AT (1) | AT350123B (pl) |
| CH (1) | CH626914A5 (pl) |
| DE (1) | DE2716610A1 (pl) |
| GB (1) | GB1601317A (pl) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2490666A1 (fr) * | 1980-08-29 | 1982-03-26 | Thomson Csf | Cristal liquide cholesterique du type reentrant, et dispositif de detection de temperature utilisant un tel cristal liquide |
| US4764619A (en) * | 1985-03-26 | 1988-08-16 | Asahi Glass Company Ltd. | Optically active compounds, smectic liquid crystal compositions containing them and smectic liquid crystal display devices |
| JPS63205319A (ja) * | 1987-02-20 | 1988-08-24 | Hitachi Ltd | シツフ結合を有する化合物，該重合体及びその製造方法 |
| GB2462617A (en) * | 2008-08-13 | 2010-02-17 | Hexcel Composites Ltd | Curing agents and means of production using kaolin clay |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4001137A (en) * | 1971-08-07 | 1977-01-04 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Nematic compounds and mixtures |
| US3827780A (en) * | 1971-10-14 | 1974-08-06 | Univ Temple | Stable anil-type nematic liquid crystals |
| US4058477A (en) * | 1972-02-23 | 1977-11-15 | Hoffmann-La Roche Inc. | Liquid crystal Schiffs bases |
| US4058478A (en) * | 1972-02-23 | 1977-11-15 | Hoffmann-La Roche Inc. | Liquid crystal esters |
| JPS4962390A (pl) * | 1972-10-17 | 1974-06-17 | ||
| US3960752A (en) * | 1972-10-24 | 1976-06-01 | Eastman Kodak Company | Liquid crystal compositions |
| US4047803A (en) * | 1973-04-24 | 1977-09-13 | Dai Nippon Toryo Kabushiki Kaisha | Nematic liquid crystal compositions |
| JPS5043076A (pl) * | 1973-08-20 | 1975-04-18 | ||
| US4009934A (en) * | 1974-01-11 | 1977-03-01 | Eastman Kodak Company | Electro-optic display devices and methods |
| US3983049A (en) * | 1974-05-02 | 1976-09-28 | General Electric Company | Liquid crystal compositions with positive dielectric anisotropy |
| US3951846A (en) * | 1974-06-28 | 1976-04-20 | Rca Corporation | Novel liquid crystal electro-optic devices |
| US4029594A (en) * | 1976-06-17 | 1977-06-14 | Rca Corporation | Novel liquid crystal compounds and electro-optic devices incorporating them |
-
1977
- 1977-03-08 CH CH286177A patent/CH626914A5/de not_active IP Right Cessation
- 1977-04-15 DE DE19772716610 patent/DE2716610A1/de not_active Withdrawn
- 1977-06-17 AT AT429477A patent/AT350123B/de not_active IP Right Cessation
-
1978
- 1978-03-02 US US05/882,742 patent/US4167489A/en not_active Expired - Lifetime
- 1978-03-06 GB GB8780/78A patent/GB1601317A/en not_active Expired
- 1978-03-08 JP JP2645578A patent/JPS53112832A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| ATA429477A (de) | 1978-10-15 |
| GB1601317A (en) | 1981-10-28 |
| JPS53112832A (en) | 1978-10-02 |
| DE2716610A1 (de) | 1978-09-14 |
| US4167489A (en) | 1979-09-11 |
| AT350123B (de) | 1979-05-10 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |