IL43521A - History 3, 4 - Dihydro - H2 - Piran - 2, 4 - Dion, their production and herbicides, mites and fungicides containing them - Google Patents
History 3, 4 - Dihydro - H2 - Piran - 2, 4 - Dion, their production and herbicides, mites and fungicides containing themInfo
- Publication number
- IL43521A IL43521A IL7343521A IL4352173A IL43521A IL 43521 A IL43521 A IL 43521A IL 7343521 A IL7343521 A IL 7343521A IL 4352173 A IL4352173 A IL 4352173A IL 43521 A IL43521 A IL 43521A
- Authority
- IL
- Israel
- Prior art keywords
- compound
- hydrogen
- ethyl
- compound according
- dihydro
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 31
- 230000002363 herbicidal effect Effects 0.000 title claims description 20
- 230000000895 acaricidal effect Effects 0.000 title claims description 7
- MERGMNQXULKBCH-UHFFFAOYSA-N pyran-2,4-dione Chemical class O=C1CC(=O)C=CO1 MERGMNQXULKBCH-UHFFFAOYSA-N 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 142
- 239000001257 hydrogen Substances 0.000 claims abstract description 26
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 26
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 24
- 230000012010 growth Effects 0.000 claims description 37
- 238000000034 method Methods 0.000 claims description 24
- -1 salt compound Chemical class 0.000 claims description 22
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- 229910052751 metal Chemical class 0.000 claims description 16
- 239000002184 metal Chemical class 0.000 claims description 16
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 230000001105 regulatory effect Effects 0.000 claims description 13
- 150000003839 salts Chemical class 0.000 claims description 13
- 125000002496 methyl group Chemical class [H]C([H])([H])* 0.000 claims description 8
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- 239000011734 sodium Substances 0.000 claims description 7
- 230000000855 fungicidal effect Effects 0.000 claims description 6
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Chemical group 0.000 claims description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 18
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 8
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- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
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- 229910052788 barium Inorganic materials 0.000 claims 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
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- 239000010949 copper Substances 0.000 claims 1
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- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims 1
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- 239000011701 zinc Substances 0.000 claims 1
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- 239000000126 substance Substances 0.000 description 20
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- 230000003449 preventive effect Effects 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003419 tautomerization reaction Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000004552 water soluble powder Substances 0.000 description 1
- 235000015099 wheat brans Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/34—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D309/36—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10496272A JPS5147773B2 (en]) | 1972-10-20 | 1972-10-20 | |
JP252673A JPS5212249B2 (en]) | 1972-12-25 | 1972-12-25 | |
JP732527A JPS5530484B2 (en]) | 1972-12-25 | 1972-12-25 |
Publications (2)
Publication Number | Publication Date |
---|---|
IL43521A0 IL43521A0 (en) | 1974-01-14 |
IL43521A true IL43521A (en) | 1977-04-29 |
Family
ID=27275399
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL7343521A IL43521A (en) | 1972-10-20 | 1973-10-30 | History 3, 4 - Dihydro - H2 - Piran - 2, 4 - Dion, their production and herbicides, mites and fungicides containing them |
Country Status (13)
Country | Link |
---|---|
US (2) | US3927034A (en]) |
AT (1) | AT331794B (en]) |
BE (1) | BE806363A (en]) |
CH (1) | CH591206A5 (en]) |
DD (2) | DD114070A5 (en]) |
DK (1) | DK134487C (en]) |
FR (1) | FR2217330B1 (en]) |
GB (1) | GB1407317A (en]) |
IL (1) | IL43521A (en]) |
IT (1) | IT1057871B (en]) |
NL (1) | NL7314373A (en]) |
OA (1) | OA04675A (en]) |
RO (1) | RO63964A (en]) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3927034A (en) * | 1972-10-20 | 1975-12-16 | Nippon Soda Co | 3,4-Dihydro-2H-pyrane-2,4-diones |
US4075239A (en) * | 1973-08-15 | 1978-02-21 | Nippon Soda Company, Limited | Cyclohexane derivatives |
JPS577122B2 (en]) * | 1973-12-24 | 1982-02-09 | ||
JPS5811841B2 (ja) * | 1974-06-04 | 1983-03-04 | 日本曹達株式会社 | オキサシクロヘキサン誘導体除草剤 |
US4001224A (en) * | 1975-03-03 | 1977-01-04 | Warner-Lambert Company | 4-substituted-2, 3-dihydro-1-benzoxepin-3, 5-diones and tautomers |
DE3239071A1 (de) * | 1982-10-22 | 1984-04-26 | Basf Ag, 6700 Ludwigshafen | Cyclohexan-1,3-dionderivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses |
CA2118796A1 (en) * | 1991-09-20 | 1993-04-01 | John Crosby | Pyranones |
WO2002007517A1 (fr) * | 2000-07-21 | 2002-01-31 | Sumitomo Chemical Company, Limited | Inhibiteurs de la biosynthèse de l'éthylène dans des plantes |
CN111072615A (zh) * | 2019-11-08 | 2020-04-28 | 聊城大学 | 3-(1-氨基亚乙基)-6-甲基吡喃-2,4-二酮衍生物的合成及其作为除草剂的应用 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3927034A (en) * | 1972-10-20 | 1975-12-16 | Nippon Soda Co | 3,4-Dihydro-2H-pyrane-2,4-diones |
-
1973
- 1973-10-15 US US406621A patent/US3927034A/en not_active Expired - Lifetime
- 1973-10-16 GB GB4808373A patent/GB1407317A/en not_active Expired
- 1973-10-17 AT AT881273A patent/AT331794B/de not_active IP Right Cessation
- 1973-10-17 CH CH1469873A patent/CH591206A5/xx not_active IP Right Cessation
- 1973-10-18 NL NL7314373A patent/NL7314373A/xx unknown
- 1973-10-19 DK DK569073A patent/DK134487C/da active
- 1973-10-19 RO RO197376384A patent/RO63964A/ro unknown
- 1973-10-19 FR FR7337489A patent/FR2217330B1/fr not_active Expired
- 1973-10-20 OA OA55041A patent/OA04675A/xx unknown
- 1973-10-22 DD DD180758*A patent/DD114070A5/xx unknown
- 1973-10-22 DD DD174214A patent/DD110161A5/xx unknown
- 1973-10-22 BE BE136937A patent/BE806363A/xx unknown
- 1973-10-22 IT IT7353259A patent/IT1057871B/it active
- 1973-10-30 IL IL7343521A patent/IL43521A/en unknown
-
1975
- 1975-07-03 US US05/592,911 patent/US3989504A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
AT331794B (de) | 1976-08-25 |
DK134487B (da) | 1976-11-15 |
DK134487C (da) | 1977-04-25 |
IT1057871B (it) | 1982-03-30 |
IL43521A0 (en) | 1974-01-14 |
FR2217330B1 (en]) | 1978-10-27 |
CH591206A5 (en]) | 1977-09-15 |
US3989504A (en) | 1976-11-02 |
DE2352661A1 (de) | 1974-05-09 |
GB1407317A (en) | 1975-09-24 |
FR2217330A1 (en]) | 1974-09-06 |
BE806363A (fr) | 1974-02-15 |
DE2352661B2 (de) | 1977-02-17 |
RO63964A (fr) | 1979-06-15 |
NL7314373A (en]) | 1974-04-23 |
DD114070A5 (en]) | 1975-07-12 |
ATA881273A (de) | 1975-12-15 |
DD110161A5 (en]) | 1974-12-12 |
US3927034A (en) | 1975-12-16 |
OA04675A (fr) | 1980-07-31 |
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