SU578820A3 - Гербицидное средство - Google Patents
Гербицидное средствоInfo
- Publication number
- SU578820A3 SU578820A3 SU7201751717A SU1751717A SU578820A3 SU 578820 A3 SU578820 A3 SU 578820A3 SU 7201751717 A SU7201751717 A SU 7201751717A SU 1751717 A SU1751717 A SU 1751717A SU 578820 A3 SU578820 A3 SU 578820A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- phenyl
- thiocarbamate
- methyl
- carbamoyloxy
- ethyl
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title description 2
- 239000004009 herbicide Substances 0.000 title 1
- 239000013543 active substance Substances 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- -1 S-methyl-N- (3- (N- (3-chlorophenyl) -carbamoyloxy) -phenyl) -thiocarbamate Chemical compound 0.000 description 50
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 8
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 description 6
- 230000006378 damage Effects 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- LAIUFBWHERIJIH-UHFFFAOYSA-N 3-Methylheptane Chemical compound CCCCC(C)CC LAIUFBWHERIJIH-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 description 1
- OLEVABUDJFFCGN-UHFFFAOYSA-N C[S+]=C(NC1=CC(OC(N2CCCCC2)=O)=CC=C1)[O-] Chemical compound C[S+]=C(NC1=CC(OC(N2CCCCC2)=O)=CC=C1)[O-] OLEVABUDJFFCGN-UHFFFAOYSA-N 0.000 description 1
- WCDOLOIGYLNBEF-UHFFFAOYSA-N C[S+]=C(NC1=CC(OC(N2CCOCC2)=O)=CC=C1)[O-] Chemical compound C[S+]=C(NC1=CC(OC(N2CCOCC2)=O)=CC=C1)[O-] WCDOLOIGYLNBEF-UHFFFAOYSA-N 0.000 description 1
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical class NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 206010039509 Scab Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000007860 aryl ester derivatives Chemical class 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C333/02—Monothiocarbamic acids; Derivatives thereof
- C07C333/08—Monothiocarbamic acids; Derivatives thereof having nitrogen atoms of thiocarbamic groups bound to carbon atoms of six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2109798A DE2109798C3 (de) | 1971-02-23 | 1971-02-23 | N-3-Carbamoyloxyphenyl-Thiolcarbamate sowie diese enthaltendes herbizides Mittel |
Publications (1)
Publication Number | Publication Date |
---|---|
SU578820A3 true SU578820A3 (ru) | 1977-10-30 |
Family
ID=5800253
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU7201751717A SU578820A3 (ru) | 1971-02-23 | 1972-02-23 | Гербицидное средство |
Country Status (24)
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2310648C3 (de) * | 1973-03-01 | 1982-05-06 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Diurethane, Verfahren zur Herstellung dieser Verbindungen sowie diese enthaltende selektive herbizide Mittel |
DE2341079C2 (de) * | 1973-08-10 | 1982-05-06 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | m-Diurethane und selektive herbizide Mittel enthaltend diese Verbindungen als Wirkstoffe |
-
1971
- 1971-02-23 DE DE2109798A patent/DE2109798C3/de not_active Expired
-
1972
- 1972-01-28 LU LU64679D patent/LU64679A1/xx unknown
- 1972-02-03 ZA ZA720714A patent/ZA72714B/xx unknown
- 1972-02-07 CS CS758A patent/CS167341B2/cs unknown
- 1972-02-09 AU AU38828/72A patent/AU476470B2/en not_active Expired
- 1972-02-14 YU YU361/72A patent/YU39578B/xx unknown
- 1972-02-14 GB GB670572A patent/GB1385802A/en not_active Expired
- 1972-02-15 SE SE7201800A patent/SE371641B/xx unknown
- 1972-02-15 IT IT20572/72A patent/IT948534B/it active
- 1972-02-17 IE IE201/72A patent/IE36115B1/xx unknown
- 1972-02-20 IL IL38799A patent/IL38799A/en unknown
- 1972-02-20 IL IL46111A patent/IL46111A/en unknown
- 1972-02-22 NO NO531/72A patent/NO135472C/no unknown
- 1972-02-22 ES ES400057A patent/ES400057A1/es not_active Expired
- 1972-02-22 DK DK82072*#A patent/DK132114C/da not_active IP Right Cessation
- 1972-02-22 DD DD161035A patent/DD95303A5/xx unknown
- 1972-02-22 FR FR7205872A patent/FR2127692A5/fr not_active Expired
- 1972-02-23 AT AT147072A patent/AT315568B/de not_active IP Right Cessation
- 1972-02-23 SU SU7201751717A patent/SU578820A3/ru active
- 1972-02-23 JP JP1884172A patent/JPS5612602B1/ja active Pending
- 1972-02-23 HU HUSCHE376*1A patent/HU164148B/hu unknown
- 1972-02-23 CA CA135,380A patent/CA975777A/en not_active Expired
- 1972-02-23 BE BE779739A patent/BE779739A/xx not_active IP Right Cessation
- 1972-02-23 NL NL7202392A patent/NL7202392A/xx not_active Application Discontinuation
- 1972-02-23 CH CH260372A patent/CH564906A5/xx not_active IP Right Cessation
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SU578820A3 (ru) | Гербицидное средство | |
SU651645A3 (ru) | Гербицидна композици | |
DE2108975C3 (de) | N-Acyl-Diurethane sowie diese enthaltendes herbizides Mittel | |
US3535101A (en) | Herbicide and algicide means | |
SU589889A3 (ru) | Гербицидное средство | |
GB988773A (en) | Sulphonyl ureas | |
US3879441A (en) | (N,-dimethyl-N-{8 3-methylmetalolycarbamyloxy)-phenyl{9 -urea | |
US3689662A (en) | Nematocidel use of 3,4,4-trifluoro-3-butenylthio methylidene compounds | |
US3510503A (en) | Trifluorobutenylthiocarbamates and thiocarbonates | |
SU644356A3 (ru) | Гербицидное средство | |
US3872157A (en) | Substituted anilide carbamates | |
SU528850A3 (ru) | Гербицидное средство | |
GB1055721A (en) | Carbamates and herbicidal compositions containing them | |
SU580801A3 (ru) | Гербицидное средство | |
US3439021A (en) | Halo-substituted phenoxyethyl carbamates and derivatives thereof | |
US3937729A (en) | Meta-bis anilide derivatives and their utility as herbicides | |
SU527127A3 (ru) | Гербицидное средство | |
SU579845A3 (ru) | Гербицидное средство | |
SU607529A3 (ru) | Гербицидное средство | |
DE2919825C2 (enrdf_load_stackoverflow) | ||
GB1355926A (en) | Herbiciedes herbicidal compositions and benzophenon derivatives | |
SU668564A3 (ru) | Гербицидное средство | |
SU528019A3 (ru) | Гербицидное средство | |
DE3318762C2 (enrdf_load_stackoverflow) | ||
DE1112728B (de) | Verfahren zur Herstellung von N-Carbaminyl-bzw. N-Thiocarbaminylamidinen |