GB872313A - Fluorine-containing derivatives of 1,3,5-triazine - Google Patents
Fluorine-containing derivatives of 1,3,5-triazineInfo
- Publication number
- GB872313A GB872313A GB2621858A GB2621858A GB872313A GB 872313 A GB872313 A GB 872313A GB 2621858 A GB2621858 A GB 2621858A GB 2621858 A GB2621858 A GB 2621858A GB 872313 A GB872313 A GB 872313A
- Authority
- GB
- United Kingdom
- Prior art keywords
- triazine
- anthraquinonylamino
- difluoro
- radical
- fluorine
- 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
- 229910052731 fluorine Inorganic materials 0.000 title abstract 4
- 239000011737 fluorine Substances 0.000 title abstract 3
- 125000003363 1,3,5-triazinyl group Chemical class N1=C(N=CN=C1)* 0.000 title 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 title 1
- -1 heterocyclic radical Chemical group 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 4
- 150000001412 amines Chemical class 0.000 abstract 3
- VMKJWLXVLHBJNK-UHFFFAOYSA-N cyanuric fluoride Chemical compound FC1=NC(F)=NC(F)=N1 VMKJWLXVLHBJNK-UHFFFAOYSA-N 0.000 abstract 3
- 238000006467 substitution reaction Methods 0.000 abstract 3
- GRFNBEZIAWKNCO-UHFFFAOYSA-N 3-pyridinol Chemical compound OC1=CC=CN=C1 GRFNBEZIAWKNCO-UHFFFAOYSA-N 0.000 abstract 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 abstract 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 abstract 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 abstract 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 abstract 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 abstract 2
- 125000001153 fluoro group Chemical group F* 0.000 abstract 2
- GVWISOJSERXQBM-UHFFFAOYSA-N n-methylpropan-1-amine Chemical compound CCCNC GVWISOJSERXQBM-UHFFFAOYSA-N 0.000 abstract 2
- ODLBCDMYCUMFSZ-IHWYPQMZSA-N (z)-2-sulfanylbut-2-enoic acid Chemical class C\C=C(/S)C(O)=O ODLBCDMYCUMFSZ-IHWYPQMZSA-N 0.000 abstract 1
- YYTSGNJTASLUOY-UHFFFAOYSA-N 1-chloropropan-2-ol Chemical compound CC(O)CCl YYTSGNJTASLUOY-UHFFFAOYSA-N 0.000 abstract 1
- NGHHCWRVKQYWQA-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;1,2,3-trichloropropane Chemical compound ClCC(Cl)CCl.OCC(CO)(CO)CO NGHHCWRVKQYWQA-UHFFFAOYSA-N 0.000 abstract 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 abstract 1
- VKPPFDPXZWFDFA-UHFFFAOYSA-N 2-chloroethanamine Chemical compound NCCCl VKPPFDPXZWFDFA-UHFFFAOYSA-N 0.000 abstract 1
- GGDYAKVUZMZKRV-UHFFFAOYSA-N 2-fluoroethanol Chemical compound OCCF GGDYAKVUZMZKRV-UHFFFAOYSA-N 0.000 abstract 1
- HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 abstract 1
- SCWNNOCLLOHZIG-UHFFFAOYSA-N 5,6,7,8-tetrahydro-1-naphthol Chemical class C1CCCC2=C1C=CC=C2O SCWNNOCLLOHZIG-UHFFFAOYSA-N 0.000 abstract 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 abstract 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007824 aliphatic compounds Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000001491 aromatic compounds Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- UENWRTRMUIOCKN-UHFFFAOYSA-N benzyl thiol Chemical class SCC1=CC=CC=C1 UENWRTRMUIOCKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000011230 binding agent Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 239000004009 herbicide Substances 0.000 abstract 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002887 hydroxy group Chemical class [H]O* 0.000 abstract 1
- 239000012442 inert solvent Substances 0.000 abstract 1
- 239000002184 metal Chemical class 0.000 abstract 1
- 150000005002 naphthylamines Chemical class 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 abstract 1
- 125000002924 primary amino group Chemical class [H]N([H])* 0.000 abstract 1
- 150000003254 radicals Chemical group 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 abstract 1
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical class OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/04—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a triazine ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF23800A DE1076696B (de) | 1957-08-21 | 1957-08-21 | Verfahren zur Herstellung fluorhaltiger Derivate des 1, 3, 5-Triazins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB872313A true GB872313A (en) | 1961-07-05 |
Family
ID=7090993
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2621858A Expired GB872313A (en) | 1957-08-21 | 1958-08-14 | Fluorine-containing derivatives of 1,3,5-triazine |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE570522A (enrdf_load_stackoverflow) |
DE (1) | DE1076696B (enrdf_load_stackoverflow) |
GB (1) | GB872313A (enrdf_load_stackoverflow) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3316264A (en) * | 1962-09-13 | 1967-04-25 | Velsicol Chemical Corp | 2-phenylthio-4-alkoxy-6-halo-s-triazines |
US4104250A (en) * | 1976-08-11 | 1978-08-01 | Borg-Warner Corporation | Flame-retardant polymers with 1,3,5-triazines having halo- and halo-aryl substitutents |
US4284772A (en) * | 1975-10-04 | 1981-08-18 | Akzona Incorporated | Monochloro-s-triazine derivatives |
US4740597A (en) * | 1984-08-21 | 1988-04-26 | Ciba-Geigy Corporation | Process for the continuous reaction of cyanuric fluoride with sulfo-containing aromatic amines |
US4968783A (en) * | 1978-06-19 | 1990-11-06 | Ciba-Geigy Corporation | Amino-fluoro-S-triazine disazo dyes of the H-acid series |
US5006645A (en) * | 1977-10-31 | 1991-04-09 | Ciba-Geigy Corporation | Dyes of the 1-sulfo-5-(2'-amino or 2'-substituted amino-4'-fluoro-5-triazin-6'-yl-aminomethyl)-naphthyl-2-azo series |
WO1994004515A1 (en) * | 1992-08-12 | 1994-03-03 | Sandoz Ltd | Method of increasing the spf rating and compounds suitable for increasing the spf rating of fibre or fabric |
CN102464625A (zh) * | 2010-11-03 | 2012-05-23 | 中国中化股份有限公司 | 一种具有除草活性的氟代三嗪类化合物及其制备方法 |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3122542A (en) * | 1959-05-06 | 1964-02-25 | Geigy Ag J R | Method for the preparation of 2, 4-diamino-6-fluoro-s-triazines |
CH638503A5 (de) | 1978-01-18 | 1983-09-30 | Ciba Geigy Ag | Verfahren zur herstellung von 2,4-difluor-6-amino-s-triazin. |
DE2850332C2 (de) * | 1978-11-20 | 1981-02-19 | Degussa Ag, 6000 Frankfurt | Verfahren zur Herstellung von substituierten 2-Mercapto-4,6-di-chlor-striazinen |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2891855A (en) * | 1954-08-16 | 1959-06-23 | Geigy Ag J R | Compositions and methods for influencing the growth of plants |
-
0
- BE BE570522D patent/BE570522A/xx unknown
-
1957
- 1957-08-21 DE DEF23800A patent/DE1076696B/de active Pending
-
1958
- 1958-08-14 GB GB2621858A patent/GB872313A/en not_active Expired
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3316264A (en) * | 1962-09-13 | 1967-04-25 | Velsicol Chemical Corp | 2-phenylthio-4-alkoxy-6-halo-s-triazines |
US4284772A (en) * | 1975-10-04 | 1981-08-18 | Akzona Incorporated | Monochloro-s-triazine derivatives |
US4104250A (en) * | 1976-08-11 | 1978-08-01 | Borg-Warner Corporation | Flame-retardant polymers with 1,3,5-triazines having halo- and halo-aryl substitutents |
US5006645A (en) * | 1977-10-31 | 1991-04-09 | Ciba-Geigy Corporation | Dyes of the 1-sulfo-5-(2'-amino or 2'-substituted amino-4'-fluoro-5-triazin-6'-yl-aminomethyl)-naphthyl-2-azo series |
US4968783A (en) * | 1978-06-19 | 1990-11-06 | Ciba-Geigy Corporation | Amino-fluoro-S-triazine disazo dyes of the H-acid series |
US4740597A (en) * | 1984-08-21 | 1988-04-26 | Ciba-Geigy Corporation | Process for the continuous reaction of cyanuric fluoride with sulfo-containing aromatic amines |
WO1994004515A1 (en) * | 1992-08-12 | 1994-03-03 | Sandoz Ltd | Method of increasing the spf rating and compounds suitable for increasing the spf rating of fibre or fabric |
US5637348A (en) * | 1992-08-12 | 1997-06-10 | Clariant Finance (Bvi) Limited | Method of increasing the SPF rating and compounds suitable for increasing the SPF rating of fibre or fabric |
AU688268B2 (en) * | 1992-08-12 | 1998-03-12 | Clariant Finance (Bvi) Limited | Method of increasing the spf rating and compounds suitable for increasing the spf rating of fibre or fabric |
CN102464625A (zh) * | 2010-11-03 | 2012-05-23 | 中国中化股份有限公司 | 一种具有除草活性的氟代三嗪类化合物及其制备方法 |
CN102464625B (zh) * | 2010-11-03 | 2014-07-02 | 中国中化股份有限公司 | 一种具有除草活性的氟代三嗪类化合物及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
BE570522A (enrdf_load_stackoverflow) | |
DE1076696B (de) | 1960-03-03 |
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