DE2349114C2 - 3-sek.-Butyl-2,1,3-benzothiadiazin-(4)-on-2,2-dioxid - Google Patents
3-sek.-Butyl-2,1,3-benzothiadiazin-(4)-on-2,2-dioxidInfo
- Publication number
- DE2349114C2 DE2349114C2 DE2349114A DE2349114A DE2349114C2 DE 2349114 C2 DE2349114 C2 DE 2349114C2 DE 2349114 A DE2349114 A DE 2349114A DE 2349114 A DE2349114 A DE 2349114A DE 2349114 C2 DE2349114 C2 DE 2349114C2
- Authority
- DE
- Germany
- Prior art keywords
- spp
- butyl
- dioxide
- benzothiadiazin
- sec
- 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
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- 240000006365 Vitis vinifera Species 0.000 description 1
- 241001506766 Xanthium Species 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 241000218496 Zeugodacus cucumis Species 0.000 description 1
- 241001148683 Zostera marina Species 0.000 description 1
- 241000159213 Zygophyllaceae Species 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000001387 apium graveolens Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 244000030166 artemisia Species 0.000 description 1
- 235000009052 artemisia Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 239000001511 capsicum annuum Substances 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 235000002532 grape seed extract Nutrition 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N heptadecan-1-ol Chemical class CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical class CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000010807 litter Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- UIHDZJYDEXIFPZ-UHFFFAOYSA-N n-butan-2-ylsulfamoyl chloride Chemical compound CCC(C)NS(Cl)(=O)=O UIHDZJYDEXIFPZ-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000001377 petroselinum spp. Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- 229940047183 tribulus Drugs 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/15—Six-membered rings
- C07D285/16—Thiadiazines; Hydrogenated thiadiazines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Priority Applications (20)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2349114A DE2349114C2 (de) | 1973-09-29 | 1973-09-29 | 3-sek.-Butyl-2,1,3-benzothiadiazin-(4)-on-2,2-dioxid |
| JP49100596A JPS5824403B2 (ja) | 1973-09-29 | 1974-09-03 | ジヨソウザイ |
| IL45593A IL45593A (en) | 1973-09-29 | 1974-09-04 | 3-substituted-1h-2,1,3-benzothiadiazin-(4)-one-2,2-dioxides,their production and their use as herbicides |
| AU72966/74A AU486220B2 (en) | 1973-09-29 | 1974-09-04 | 2,1,3-benzothiadiazin-(4)-one-2,2-doixides |
| CA209,135A CA1015756A (en) | 1973-09-29 | 1974-09-12 | 2,1,3-benzothiadiazin-(4)-one-2,2-dioxides |
| NL7412128A NL7412128A (nl) | 1973-09-29 | 1974-09-12 | Werkwijze ter bereiding van 2,1,3-benzothiadia- 4)on 2,2-dioxyden. |
| US05/506,559 US3997531A (en) | 1973-09-29 | 1974-09-16 | 2,1,3-Benzothiadiazin-(4)-one-2,2-dioxides |
| CS7400006628A CS181771B2 (en) | 1973-09-29 | 1974-09-20 | Herbicidal agent |
| YU02578/74A YU257874A (en) | 1973-09-29 | 1974-09-24 | Process for obtaining new 2,1,3-benzothiadiazine-(4)-one-2,2-dioxide derivatives |
| IT53199/74A IT1050244B (it) | 1973-09-29 | 1974-09-25 | 2 1 3 benzotiadiazin 4 one 2 2 biossidi |
| CH1295274A CH585011A5 (en:Method) | 1973-09-29 | 1974-09-25 | |
| HUBA3147A HU170666B (en:Method) | 1973-09-29 | 1974-09-27 | |
| ZA00746144A ZA746144B (en) | 1973-09-29 | 1974-09-27 | 2,1,3-benzothiadiazin-(4)-one-2,2,-dioxides |
| FR7432642A FR2245647B1 (en:Method) | 1973-09-29 | 1974-09-27 | |
| DD181381A DD113987A5 (en:Method) | 1973-09-29 | 1974-09-27 | |
| BE149013A BE820479A (fr) | 1973-09-29 | 1974-09-27 | Nouveaux derives du 2 |
| SU2062509A SU540550A3 (ru) | 1973-09-29 | 1974-09-27 | Гербицидное средство |
| AT780574A AT334131B (de) | 1973-09-29 | 1974-09-27 | Herbizid |
| PL1974174373A PL89744B1 (en:Method) | 1973-09-29 | 1974-09-27 | |
| DK511174A DK137727C (da) | 1973-09-29 | 1974-09-27 | Substituerede 2,1,3-benzothiadiazin-(4)-on-2,2-dioxider til anvendelse som herbicider |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2349114A DE2349114C2 (de) | 1973-09-29 | 1973-09-29 | 3-sek.-Butyl-2,1,3-benzothiadiazin-(4)-on-2,2-dioxid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2349114A1 DE2349114A1 (de) | 1975-04-10 |
| DE2349114C2 true DE2349114C2 (de) | 1985-11-14 |
Family
ID=5894145
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2349114A Expired DE2349114C2 (de) | 1973-09-29 | 1973-09-29 | 3-sek.-Butyl-2,1,3-benzothiadiazin-(4)-on-2,2-dioxid |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US3997531A (en:Method) |
| JP (1) | JPS5824403B2 (en:Method) |
| AT (1) | AT334131B (en:Method) |
| BE (1) | BE820479A (en:Method) |
| CA (1) | CA1015756A (en:Method) |
| CH (1) | CH585011A5 (en:Method) |
| CS (1) | CS181771B2 (en:Method) |
| DD (1) | DD113987A5 (en:Method) |
| DE (1) | DE2349114C2 (en:Method) |
| DK (1) | DK137727C (en:Method) |
| FR (1) | FR2245647B1 (en:Method) |
| HU (1) | HU170666B (en:Method) |
| IL (1) | IL45593A (en:Method) |
| IT (1) | IT1050244B (en:Method) |
| NL (1) | NL7412128A (en:Method) |
| PL (1) | PL89744B1 (en:Method) |
| SU (1) | SU540550A3 (en:Method) |
| YU (1) | YU257874A (en:Method) |
| ZA (1) | ZA746144B (en:Method) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2458343A1 (de) * | 1974-12-10 | 1976-06-16 | Basf Ag | N-n'-disubstituierte 2,1,3-benzothiadiazin(4)on-2.2-dioxide |
| DE2553209C2 (de) * | 1975-11-27 | 1986-01-02 | Basf Ag, 6700 Ludwigshafen | 1-Methoxymethyl-3-isopropyl-2,1,3-benzothiadiazin(4)on-2,2-dioxid und diese enthaltende Herbizide |
| US4208514A (en) * | 1976-02-23 | 1980-06-17 | The Dow Chemical Company | 4(3H)-Oxobenzo-2,1,3-thiadiazine-2,2-dioxides |
| DE2656290A1 (de) * | 1976-12-11 | 1978-06-15 | Basf Ag | Benzothiadiazinverbindungen |
| US4226867A (en) * | 1978-10-06 | 1980-10-07 | Merck & Co., Inc. | 3,3-Substituted spiro-1,2,4-benzothiadiazines |
| DE2852274A1 (de) * | 1978-12-02 | 1980-06-19 | Basf Ag | Verfahren zur herstellung von sulfamidsaeurehalogeniden |
| CN108744706A (zh) * | 2018-06-08 | 2018-11-06 | 福建省东南电化股份有限公司 | 一种光气溶液自动过滤装置 |
| CN109574125A (zh) * | 2019-01-28 | 2019-04-05 | 太原理工大学 | 酸性老窑水修复方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2105687C2 (de) * | 1971-02-08 | 1981-09-24 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von 3-substituierten 2,1,3-Benzothiadiazin-4-on-2,2-dioxiden |
| BE793238A (fr) * | 1971-12-24 | 1973-06-22 | Basf Ag | Procede de lutte contre la croissance de plantes indesirables |
-
1973
- 1973-09-29 DE DE2349114A patent/DE2349114C2/de not_active Expired
-
1974
- 1974-09-03 JP JP49100596A patent/JPS5824403B2/ja not_active Expired
- 1974-09-04 IL IL45593A patent/IL45593A/en unknown
- 1974-09-12 NL NL7412128A patent/NL7412128A/xx not_active Application Discontinuation
- 1974-09-12 CA CA209,135A patent/CA1015756A/en not_active Expired
- 1974-09-16 US US05/506,559 patent/US3997531A/en not_active Expired - Lifetime
- 1974-09-20 CS CS7400006628A patent/CS181771B2/cs unknown
- 1974-09-24 YU YU02578/74A patent/YU257874A/xx unknown
- 1974-09-25 CH CH1295274A patent/CH585011A5/xx not_active IP Right Cessation
- 1974-09-25 IT IT53199/74A patent/IT1050244B/it active
- 1974-09-27 PL PL1974174373A patent/PL89744B1/pl unknown
- 1974-09-27 HU HUBA3147A patent/HU170666B/hu not_active IP Right Cessation
- 1974-09-27 DK DK511174A patent/DK137727C/da not_active IP Right Cessation
- 1974-09-27 BE BE149013A patent/BE820479A/xx not_active IP Right Cessation
- 1974-09-27 FR FR7432642A patent/FR2245647B1/fr not_active Expired
- 1974-09-27 AT AT780574A patent/AT334131B/de not_active IP Right Cessation
- 1974-09-27 ZA ZA00746144A patent/ZA746144B/xx unknown
- 1974-09-27 SU SU2062509A patent/SU540550A3/ru active
- 1974-09-27 DD DD181381A patent/DD113987A5/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| YU257874A (en) | 1982-02-28 |
| DK511174A (en:Method) | 1975-05-26 |
| BE820479A (fr) | 1975-03-27 |
| IL45593A (en) | 1977-02-28 |
| ZA746144B (en) | 1975-11-26 |
| CA1015756A (en) | 1977-08-16 |
| DD113987A5 (en:Method) | 1975-07-12 |
| IT1050244B (it) | 1981-03-10 |
| DE2349114A1 (de) | 1975-04-10 |
| ATA780574A (de) | 1976-04-15 |
| HU170666B (en:Method) | 1977-08-28 |
| SU540550A3 (ru) | 1976-12-25 |
| AT334131B (de) | 1976-12-27 |
| JPS5824403B2 (ja) | 1983-05-20 |
| CS181771B2 (en) | 1978-03-31 |
| DK137727B (da) | 1978-04-24 |
| IL45593A0 (en) | 1974-11-29 |
| US3997531A (en) | 1976-12-14 |
| FR2245647A1 (en:Method) | 1975-04-25 |
| CH585011A5 (en:Method) | 1977-02-28 |
| NL7412128A (nl) | 1975-04-02 |
| PL89744B1 (en:Method) | 1976-12-31 |
| JPS5063138A (en:Method) | 1975-05-29 |
| DK137727C (da) | 1978-10-02 |
| AU7296674A (en) | 1976-03-11 |
| FR2245647B1 (en:Method) | 1978-11-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OD | Request for examination | ||
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |