DE1963196A1 - Benzobisoxazole - Google Patents
BenzobisoxazoleInfo
- Publication number
- DE1963196A1 DE1963196A1 DE19691963196 DE1963196A DE1963196A1 DE 1963196 A1 DE1963196 A1 DE 1963196A1 DE 19691963196 DE19691963196 DE 19691963196 DE 1963196 A DE1963196 A DE 1963196A DE 1963196 A1 DE1963196 A1 DE 1963196A1
- Authority
- DE
- Germany
- Prior art keywords
- analysis
- benzo
- bisoxazole
- bie
- reaction
- 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
- 150000001875 compounds Chemical class 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 239000007859 condensation product Substances 0.000 claims description 2
- 125000005605 benzo group Chemical group 0.000 claims 2
- 241001024304 Mino Species 0.000 claims 1
- 150000001299 aldehydes Chemical class 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 150000003851 azoles Chemical class 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 101150032765 ARNTL gene Proteins 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- -1 alkyl radicals Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 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
- 229940117916 cinnamic aldehyde Drugs 0.000 description 1
- ATDGTVJJHBUTRL-UHFFFAOYSA-N cyanogen bromide Chemical compound BrC#N ATDGTVJJHBUTRL-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 210000002837 heart atrium Anatomy 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- BLTAPEIEHGWKKN-UHFFFAOYSA-N methanesulfonate;pyridin-1-ium Chemical compound CS(O)(=O)=O.C1=CC=NC=C1 BLTAPEIEHGWKKN-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920002382 photo conductive polymer Polymers 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 210000002435 tendon Anatomy 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0622—Heterocyclic compounds
- G03G5/0644—Heterocyclic compounds containing two or more hetero rings
- G03G5/0646—Heterocyclic compounds containing two or more hetero rings in the same ring system
- G03G5/065—Heterocyclic compounds containing two or more hetero rings in the same ring system containing three relevant rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US78993069A | 1969-01-08 | 1969-01-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1963196A1 true DE1963196A1 (de) | 1970-07-23 |
Family
ID=25149143
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19691963196 Pending DE1963196A1 (de) | 1969-01-08 | 1969-12-17 | Benzobisoxazole |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE1963196A1 (enrdf_load_stackoverflow) |
FR (1) | FR2027894A1 (enrdf_load_stackoverflow) |
GB (1) | GB1287871A (enrdf_load_stackoverflow) |
-
1969
- 1969-12-11 FR FR6942820A patent/FR2027894A1/fr not_active Withdrawn
- 1969-12-17 DE DE19691963196 patent/DE1963196A1/de active Pending
-
1970
- 1970-01-01 GB GB13270A patent/GB1287871A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
GB1287871A (enrdf_load_stackoverflow) | 1972-09-06 |
FR2027894A1 (enrdf_load_stackoverflow) | 1970-10-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH318461A (fr) | Procédé de fabrication de papier couché et appareil pour l'exécution de ce procédé | |
DE2235051C3 (de) | Verfahren zur Herstellung von Novolaken | |
DE1595724A1 (de) | Verfahren zur Herstellung von Polybenzoxazolen | |
DE2004766C3 (enrdf_load_stackoverflow) | ||
DE3317570A1 (de) | Verfahren zur haertung von saeurehaertbaren schleifmittel-zusammensetzungen | |
DE1963196A1 (de) | Benzobisoxazole | |
DE1644619A1 (de) | Verfahren zur Herstellung von Farbstoffen der Triphenylrosanilinreihe | |
DE1670680A1 (de) | Verfahren zur Herstellung von 3,1-Benzothiazin-Derivaten | |
DE1817703A1 (de) | Verfahren zur Herstellung von Imidazolidinen sowie neue Imidazolidinverbindungen | |
DE2335332A1 (de) | 1-hydroxy-2-(substituierte-anilino) chinoliziniumbromide | |
DE406999C (de) | Verfahren zur Darstellung von kuenstlichen Harzen und OElen | |
DE2843233C2 (de) | Gerbstoff und dessen Verwendung | |
DE2504925A1 (de) | Verfahren zur herstellung von xanthenfarbstoffen | |
DE1797297C3 (de) | Benzobisthiazole und deren Verwendung in elektrophotographischen Verfahren | |
DE1235942B (de) | Verfahren zur Herstellung von alkaliloeslichen Kondensationsprodukten | |
DE863057C (de) | Verfahren zur Herstellung wasserloeslicher Kondensationsprodukte | |
DE654002C (de) | Verfahren zur Herstellung von blau bis schwarz faerbenden Schwefelfarbstoffen | |
DE910199C (de) | Verfahren zur Herstellung von Merocyaninen | |
DE2247917A1 (de) | Verfahren zum haerten von phenolharzen | |
DE2630474A1 (de) | Verfahren zur herstellung von tetrahydrothieno(3,2-c)- bzw. -(2,3-c) pyridinderivaten | |
DE899042C (de) | Verfahren zur Herstellung von neuen 4, 4'-Diaminostilbendisulfon- oder -dicarbonsaeuren | |
AT221213B (de) | Synthetische Weißgerbstoffe | |
DE1126368B (de) | Verfahren zur Herstellung von Aldehyden mit quartaerem ª‡-Kohlenstoffatom | |
AT130936B (de) | Verfahren zur Darstellung von Thioderivaten der Phenole. | |
DE721197C (de) | Verfahren zur Herstellung eines harzartigen Kondensationsstoffes aus Cumaronharzoelen |