MX3101E - Metodo para preparar el 1 , 1 , 4 , 4 - tetr oxido de 2 , 3 - di hidro - 1 , 4 - di ti ina - Google Patents
Metodo para preparar el 1 , 1 , 4 , 4 - tetr oxido de 2 , 3 - di hidro - 1 , 4 - di ti inaInfo
- Publication number
- MX3101E MX3101E MX004719U MX471975U MX3101E MX 3101 E MX3101 E MX 3101E MX 004719 U MX004719 U MX 004719U MX 471975 U MX471975 U MX 471975U MX 3101 E MX3101 E MX 3101E
- Authority
- MX
- Mexico
- Prior art keywords
- acid
- formula
- group
- dithine
- dihydro
- Prior art date
Links
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 150000004965 peroxy acids Chemical class 0.000 abstract 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 2
- PCGDBWLKAYKBTN-UHFFFAOYSA-N 1,2-dithiole Chemical compound C1SSC=C1 PCGDBWLKAYKBTN-UHFFFAOYSA-N 0.000 abstract 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 abstract 1
- LJGHYPLBDBRCRZ-UHFFFAOYSA-N 3-(3-aminophenyl)sulfonylaniline Chemical compound NC1=CC=CC(S(=O)(=O)C=2C=C(N)C=CC=2)=C1 LJGHYPLBDBRCRZ-UHFFFAOYSA-N 0.000 abstract 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 1
- 239000003377 acid catalyst Substances 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004849 alkoxymethyl group Chemical group 0.000 abstract 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 abstract 1
- 229940092714 benzenesulfonic acid Drugs 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 1
- 235000019253 formic acid Nutrition 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 1
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 235000019260 propionic acid Nutrition 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
- A01N43/32—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D339/00—Heterocyclic compounds containing rings having two sulfur atoms as the only ring hetero atoms
- C07D339/08—Six-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/481,010 US4004018A (en) | 1974-06-20 | 1974-06-20 | 2,3-Dihydro-1,4-dithiin 1,1,4,4-tetroxide antimicrobials |
| DE19762626063 DE2626063A1 (de) | 1974-06-20 | 1976-06-10 | Fungizide bzw. bakterizide 2,3-dihydro-1,4-dithiin-1,1,4,4-tetroxide und deren verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX3101E true MX3101E (es) | 1980-04-09 |
Family
ID=25770556
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX004719U MX3101E (es) | 1974-06-20 | 1975-06-11 | Metodo para preparar el 1 , 1 , 4 , 4 - tetr oxido de 2 , 3 - di hidro - 1 , 4 - di ti ina |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US4004018A (enExample) |
| JP (1) | JPS5946201B2 (enExample) |
| AR (1) | AR220091A1 (enExample) |
| CA (1) | CA1046069A (enExample) |
| DD (1) | DD119964A5 (enExample) |
| DE (2) | DE2527639C2 (enExample) |
| FR (1) | FR2275148A1 (enExample) |
| GB (2) | GB1476409A (enExample) |
| MX (1) | MX3101E (enExample) |
| NL (1) | NL187241C (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4004018A (en) * | 1974-06-20 | 1977-01-18 | Uniroyal Inc. | 2,3-Dihydro-1,4-dithiin 1,1,4,4-tetroxide antimicrobials |
| US4276422A (en) * | 1975-01-10 | 1981-06-30 | Uniroyal, Inc. | Substituted dithiin tetroxide plant growth regulants |
| CA1150284A (en) * | 1980-12-02 | 1983-07-19 | Allan K.S. Tsai | Method of making certain 2,3-dihydro-1,4-dithiins |
| JPS63134129A (ja) * | 1986-11-26 | 1988-06-06 | Yoshinobu Kobayashi | 超硬工具の製法 |
| JPH01153229A (ja) * | 1987-01-14 | 1989-06-15 | Yoshinobu Kobayashi | 超硬工具の製法 |
| JPS63180427A (ja) * | 1987-01-22 | 1988-07-25 | Yoshinobu Kobayashi | 超硬工具の製法 |
| JPH0181208U (enExample) * | 1987-11-19 | 1989-05-31 | ||
| US5268389A (en) | 1989-10-16 | 1993-12-07 | Uniroyal Chemical Company, Inc. | Thiocarboxylate ester compounds compositions containing the same |
| JPH083040A (ja) * | 1994-06-21 | 1996-01-09 | Soyaku Gijutsu Kenkyusho:Kk | ベンゾジチイン誘導体を有効成分とする抗ウイルス剤 |
| US6407136B1 (en) | 1999-05-21 | 2002-06-18 | Ortho-Mcneil Pharmaceutical, Inc. | 1,4-dithiin and 1,4-dithiepin-1,1,4,4, tetroxide derivatives useful as antagonists of the human galanin receptor |
| WO2000071533A2 (en) * | 1999-05-21 | 2000-11-30 | Ortho-Mcneil Pharmaceutical, Inc. | 1,4-dithiin and 1,4-dithiepin- 1,1,4,4, tetroxide derivatives useful as antagonists of the human galanin receptor |
| PL2386203T3 (pl) * | 2008-10-15 | 2014-05-30 | Bayer Ip Gmbh | Zastosowanie ditiino-tetrakarboksyimidów do zwalczania fitopatogennych grzybów |
| WO2011128301A1 (de) | 2010-04-14 | 2011-10-20 | Bayer Cropscience Ag | Dithiin-derivate als fungizide |
| US20120142676A1 (en) | 2010-08-18 | 2012-06-07 | Gaik-Lean Chee | Oxathiazine and dithiine oxides as inhibitors of sulfhydryl-dependent biomolecules |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3503991A (en) * | 1966-11-14 | 1970-03-31 | Stauffer Chemical Co | Synthesis of para-dithianes |
| US3439051A (en) * | 1967-01-13 | 1969-04-15 | Dow Chemical Co | 2,3-dihydro-1,4-dithiins as stabilizers for chlorinated hydrocarbons |
| DE1957860A1 (de) * | 1969-11-18 | 1971-05-27 | Degussa | Verfahren zur Herstellung von 2,3-Dihydro-p-dithiinen und deren Sulfoxiden und Sulfonen |
| US3997323A (en) * | 1973-05-07 | 1976-12-14 | Uniroyal Inc. | Herbicidal method employing substituted dithin tetroxides |
| US4004018A (en) * | 1974-06-20 | 1977-01-18 | Uniroyal Inc. | 2,3-Dihydro-1,4-dithiin 1,1,4,4-tetroxide antimicrobials |
-
1974
- 1974-06-20 US US05/481,010 patent/US4004018A/en not_active Expired - Lifetime
- 1974-11-19 CA CA214,110A patent/CA1046069A/en not_active Expired
-
1975
- 1975-05-30 AR AR259032A patent/AR220091A1/es active
- 1975-06-09 GB GB2464575A patent/GB1476409A/en not_active Expired
- 1975-06-09 GB GB2141576A patent/GB1476410A/en not_active Expired
- 1975-06-11 MX MX004719U patent/MX3101E/es unknown
- 1975-06-18 DD DD186733A patent/DD119964A5/xx unknown
- 1975-06-19 FR FR7519256A patent/FR2275148A1/fr active Granted
- 1975-06-19 JP JP50075013A patent/JPS5946201B2/ja not_active Expired
- 1975-06-20 NL NLAANVRAGE7507419,A patent/NL187241C/xx not_active IP Right Cessation
- 1975-06-20 DE DE2527639A patent/DE2527639C2/de not_active Expired
-
1976
- 1976-06-10 DE DE19762626063 patent/DE2626063A1/de not_active Ceased
- 1976-11-18 US US05/742,933 patent/US4097580A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| NL187241C (nl) | 1991-07-16 |
| NL187241B (nl) | 1991-02-18 |
| DE2626063A1 (de) | 1977-12-22 |
| AR220091A1 (es) | 1980-10-15 |
| CA1046069A (en) | 1979-01-09 |
| NL7507419A (nl) | 1975-12-23 |
| DE2527639A1 (de) | 1976-01-15 |
| GB1476410A (en) | 1977-06-16 |
| FR2275148B1 (enExample) | 1980-05-16 |
| JPS5946201B2 (ja) | 1984-11-10 |
| US4004018A (en) | 1977-01-18 |
| JPS5115628A (en) | 1976-02-07 |
| US4097580A (en) | 1978-06-27 |
| FR2275148A1 (fr) | 1976-01-16 |
| DD119964A5 (enExample) | 1976-05-20 |
| GB1476409A (en) | 1977-06-16 |
| DE2527639C2 (de) | 1985-10-03 |
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