DD148709A5 - Herbizide mittel - Google Patents
Herbizide mittel Download PDFInfo
- Publication number
- DD148709A5 DD148709A5 DD80218424A DD21842480A DD148709A5 DD 148709 A5 DD148709 A5 DD 148709A5 DD 80218424 A DD80218424 A DD 80218424A DD 21842480 A DD21842480 A DD 21842480A DD 148709 A5 DD148709 A5 DD 148709A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- ester
- acid
- fluoro
- phenyl
- ethyl
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title claims abstract description 7
- 230000002363 herbicidal effect Effects 0.000 title abstract description 10
- 150000001875 compounds Chemical class 0.000 claims abstract description 34
- 239000000203 mixture Substances 0.000 claims abstract description 7
- 239000000969 carrier Substances 0.000 claims abstract description 6
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052731 fluorine Chemical group 0.000 claims abstract description 3
- 239000011737 fluorine Chemical group 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 3
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 3
- 239000001301 oxygen Substances 0.000 claims abstract description 3
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims abstract description 3
- 239000011593 sulfur Chemical group 0.000 claims abstract description 3
- 229910052717 sulfur Chemical group 0.000 claims abstract description 3
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims abstract 3
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 claims description 2
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 abstract description 17
- 239000003795 chemical substances by application Substances 0.000 abstract description 8
- 229920000742 Cotton Polymers 0.000 abstract description 3
- 125000000304 alkynyl group Chemical group 0.000 abstract description 3
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 101100072620 Streptomyces griseus ind2 gene Proteins 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- -1 uracils Chemical class 0.000 description 84
- 150000002148 esters Chemical class 0.000 description 69
- 239000002253 acid Substances 0.000 description 32
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 16
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- MGDDHBBPSNIXFW-UHFFFAOYSA-N (3-fluorophenyl)-methylcarbamic acid Chemical compound OC(=O)N(C)C1=CC=CC(F)=C1 MGDDHBBPSNIXFW-UHFFFAOYSA-N 0.000 description 9
- 235000002634 Solanum Nutrition 0.000 description 9
- 241000207763 Solanum Species 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 235000011331 Brassica Nutrition 0.000 description 8
- 241000219198 Brassica Species 0.000 description 8
- WZOMBBOIBCHWCP-UHFFFAOYSA-N (4-fluorophenyl)-methylcarbamic acid Chemical compound OC(=O)N(C)C1=CC=C(F)C=C1 WZOMBBOIBCHWCP-UHFFFAOYSA-N 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- DJTODVVYZSSTCR-UHFFFAOYSA-N ethyl-(3-fluorophenyl)carbamic acid Chemical compound CCN(C(O)=O)C1=CC=CC(F)=C1 DJTODVVYZSSTCR-UHFFFAOYSA-N 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- CNRYLCJODAIULK-UHFFFAOYSA-N (2-fluorophenyl)-(2-phenylethyl)carbamic acid Chemical compound FC1=C(N(C(O)=O)CCC2=CC=CC=C2)C=CC=C1 CNRYLCJODAIULK-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- QVUFBHNIVPPFEI-UHFFFAOYSA-N (3-fluorophenyl)-(2-phenylethyl)carbamic acid Chemical compound FC=1C=C(N(C(O)=O)CCC2=CC=CC=C2)C=CC1 QVUFBHNIVPPFEI-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- CQMPIKBKOLXRPU-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] N-ethyl-N-(3-fluorophenyl)carbamate Chemical compound C(C)OC(=O)NC=1C=C(C=CC1)OC(N(C1=CC(=CC=C1)F)CC)=O CQMPIKBKOLXRPU-UHFFFAOYSA-N 0.000 description 3
- GUQLNCYGMDJFGO-UHFFFAOYSA-N [3-(methoxycarbonylamino)phenyl] N-(4-fluorophenyl)-N-methylcarbamate Chemical compound COC(=O)NC=1C=C(C=CC1)OC(N(C1=CC=C(C=C1)F)C)=O GUQLNCYGMDJFGO-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 150000007530 organic bases Chemical group 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- PCBXHSGXUDAMAR-UHFFFAOYSA-N (3,4-difluorophenyl)-ethylcarbamic acid Chemical compound CCN(C(O)=O)C1=CC=C(F)C(F)=C1 PCBXHSGXUDAMAR-UHFFFAOYSA-N 0.000 description 2
- PATNMSXWIVJSHC-UHFFFAOYSA-N (3-fluorophenyl)-propylcarbamic acid Chemical compound FC=1C=C(N(C(O)=O)CCC)C=CC1 PATNMSXWIVJSHC-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241001553178 Arachis glabrata Species 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- FQMCQYMAKONBDT-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] N-(4-fluorophenyl)-N-methylcarbamate Chemical compound C(C)OC(=O)NC=1C=C(C=CC1)OC(N(C1=CC=C(C=C1)F)C)=O FQMCQYMAKONBDT-UHFFFAOYSA-N 0.000 description 2
- MHRVTXVWOWITHP-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] N-ethyl-N-(4-fluorophenyl)carbamate Chemical compound C(C)OC(=O)NC=1C=C(C=CC1)OC(N(C1=CC=C(C=C1)F)CC)=O MHRVTXVWOWITHP-UHFFFAOYSA-N 0.000 description 2
- VLCYJUKOBQMFTC-UHFFFAOYSA-N [3-(methoxycarbonylamino)phenyl] N-(3,4-difluorophenyl)-N-ethylcarbamate Chemical compound COC(=O)NC=1C=C(C=CC1)OC(N(C1=CC(=C(C=C1)F)F)CC)=O VLCYJUKOBQMFTC-UHFFFAOYSA-N 0.000 description 2
- CUQAZLABXWMPDB-UHFFFAOYSA-N [3-(methoxycarbonylamino)phenyl] N-(3-fluorophenyl)-N-methylcarbamate Chemical class COC(=O)NC=1C=C(C=CC1)OC(N(C1=CC(=CC=C1)F)C)=O CUQAZLABXWMPDB-UHFFFAOYSA-N 0.000 description 2
- IVNSQRACXWLZCI-UHFFFAOYSA-N [3-(methoxycarbonylamino)phenyl] N-ethyl-N-(2-fluorophenyl)carbamate Chemical compound COC(=O)NC=1C=C(C=CC1)OC(N(C1=C(C=CC=C1)F)CC)=O IVNSQRACXWLZCI-UHFFFAOYSA-N 0.000 description 2
- VCJUJZHGRYCPGJ-UHFFFAOYSA-N butyl-(4-fluorophenyl)carbamic acid Chemical compound CCCCN(C(O)=O)C1=CC=C(F)C=C1 VCJUJZHGRYCPGJ-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- BSAYWCZHCBTSCD-UHFFFAOYSA-N ethyl-(2-fluorophenyl)carbamic acid Chemical compound CCN(C(O)=O)C1=CC=CC=C1F BSAYWCZHCBTSCD-UHFFFAOYSA-N 0.000 description 2
- 150000007529 inorganic bases Chemical class 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- FTLCLAFMYWOANF-UHFFFAOYSA-N (2-fluorophenyl)carbamic acid Chemical compound OC(=O)NC1=CC=CC=C1F FTLCLAFMYWOANF-UHFFFAOYSA-N 0.000 description 1
- KPRWEGORVIVZNZ-UHFFFAOYSA-N (4-fluorophenyl)-(2-phenylethyl)carbamic acid Chemical compound FC1=CC=C(N(C(O)=O)CCC2=CC=CC=C2)C=C1 KPRWEGORVIVZNZ-UHFFFAOYSA-N 0.000 description 1
- IDUFFHCIDXAHEZ-UHFFFAOYSA-N (4-fluorophenyl)-propylcarbamic acid Chemical compound FC1=CC=C(N(C(O)=O)CCC)C=C1 IDUFFHCIDXAHEZ-UHFFFAOYSA-N 0.000 description 1
- QVVJZHVEBUNKBZ-UHFFFAOYSA-N (4-fluorophenyl)carbamic acid Chemical compound OC(=O)NC1=CC=C(F)C=C1 QVVJZHVEBUNKBZ-UHFFFAOYSA-N 0.000 description 1
- GIRGFOHZHDGCJA-UHFFFAOYSA-N 2-[(2,3,6-trichlorophenyl)methoxy]propan-2-ol Chemical compound CC(C)(O)OCC1=C(Cl)C=CC(Cl)=C1Cl GIRGFOHZHDGCJA-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- JSIAIROWMJGMQZ-UHFFFAOYSA-N 2h-triazol-4-amine Chemical class NC1=CNN=N1 JSIAIROWMJGMQZ-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000219318 Amaranthus Species 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 241000335053 Beta vulgaris Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical class NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 244000192528 Chrysanthemum parthenium Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 235000017945 Matricaria Nutrition 0.000 description 1
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 240000006394 Sorghum bicolor Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 240000006694 Stellaria media Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- HAIGJRYOZZPZCC-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] N-(3,4-difluorophenyl)-N-ethylcarbamate Chemical compound C(C)OC(=O)NC=1C=C(C=CC1)OC(N(C1=CC(=C(C=C1)F)F)CC)=O HAIGJRYOZZPZCC-UHFFFAOYSA-N 0.000 description 1
- CNEHQBOPRCQXOD-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] N-(3-fluorophenyl)-N-(2-phenylethyl)carbamate Chemical compound C(C)OC(=O)NC=1C=C(C=CC1)OC(N(C1=CC(=CC=C1)F)CCC1=CC=CC=C1)=O CNEHQBOPRCQXOD-UHFFFAOYSA-N 0.000 description 1
- OXHJYBHEDUETFK-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] N-(3-fluorophenyl)-N-methylcarbamate Chemical compound C(C)OC(=O)NC=1C=C(C=CC1)OC(N(C1=CC(=CC=C1)F)C)=O OXHJYBHEDUETFK-UHFFFAOYSA-N 0.000 description 1
- PZHRYULMUNEGCI-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] n-(3,4-difluorophenyl)carbamate Chemical compound CCOC(=O)NC1=CC=CC(OC(=O)NC=2C=C(F)C(F)=CC=2)=C1 PZHRYULMUNEGCI-UHFFFAOYSA-N 0.000 description 1
- JKUIWGXGCPXROH-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] n-(3-chloro-4-fluorophenyl)carbamate Chemical compound CCOC(=O)NC1=CC=CC(OC(=O)NC=2C=C(Cl)C(F)=CC=2)=C1 JKUIWGXGCPXROH-UHFFFAOYSA-N 0.000 description 1
- ZKXKGPVPQDYNCY-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] n-methyl-n-phenylcarbamate Chemical class CCOC(=O)NC1=CC=CC(OC(=O)N(C)C=2C=CC=CC=2)=C1 ZKXKGPVPQDYNCY-UHFFFAOYSA-N 0.000 description 1
- IPZQWWZBDMZXGK-UHFFFAOYSA-N [3-(methoxycarbonylamino)phenyl] N-(2-fluorophenyl)-N-(2-phenylethyl)carbamate Chemical compound COC(=O)NC=1C=C(C=CC1)OC(N(C1=C(C=CC=C1)F)CCC1=CC=CC=C1)=O IPZQWWZBDMZXGK-UHFFFAOYSA-N 0.000 description 1
- ZSZYRSNFJDADEE-UHFFFAOYSA-N [3-(methoxycarbonylamino)phenyl] N-(3-fluorophenyl)-N-propylcarbamate Chemical compound COC(=O)NC=1C=C(C=CC1)OC(N(C1=CC(=CC=C1)F)CCC)=O ZSZYRSNFJDADEE-UHFFFAOYSA-N 0.000 description 1
- ZOXXVYOXSGKIES-UHFFFAOYSA-N [3-(methoxycarbonylamino)phenyl] N-ethyl-N-(3-fluorophenyl)carbamate Chemical compound COC(=O)NC=1C=C(C=CC1)OC(N(C1=CC(=CC=C1)F)CC)=O ZOXXVYOXSGKIES-UHFFFAOYSA-N 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- IMNFDUFMRHMDMM-UHFFFAOYSA-N anhydrous n-heptane Natural products CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 1
- 229940051881 anilide analgesics and antipyretics Drugs 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000001559 benzoic acids Chemical class 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical compound OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 1
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 150000004891 diazines Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
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- 230000001882 diuretic effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000006627 ethoxycarbonylamino group Chemical group 0.000 description 1
- UAEPXXFSZDCODC-UHFFFAOYSA-N ethyl-(4-fluorophenyl)carbamic acid Chemical compound C(C)N(C(O)=O)C1=CC=C(C=C1)F UAEPXXFSZDCODC-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000003977 halocarboxylic acids Chemical class 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 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
- 239000006028 limestone Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- SBNPVCZGSKLRSJ-UHFFFAOYSA-N n-ethyl-3-fluoroaniline Chemical compound CCNC1=CC=CC(F)=C1 SBNPVCZGSKLRSJ-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 210000002741 palatine tonsil Anatomy 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- OLTPKMBOLARPFC-UHFFFAOYSA-N phenyl(2-phenylethyl)carbamic acid Chemical compound C=1C=CC=CC=1N(C(=O)O)CCC1=CC=CC=C1 OLTPKMBOLARPFC-UHFFFAOYSA-N 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003560 thiocarbamic acids Chemical class 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19792901658 DE2901658A1 (de) | 1979-01-15 | 1979-01-15 | Diurethane, verfahren zur herstellung dieser verbindungen sowie diese enthaltende herbizide mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD148709A5 true DD148709A5 (de) | 1981-06-10 |
Family
ID=6060757
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD80218424A DD148709A5 (de) | 1979-01-15 | 1980-01-11 | Herbizide mittel |
Country Status (35)
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1567151C3 (de) * | 1965-04-09 | 1974-02-21 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Diurethane, Verfahren zur Herstellung dieser Verbindungen sowie diese enthaltende herbizide Mittel |
| US3535101A (en) * | 1966-09-07 | 1970-10-20 | Schering Ag | Herbicide and algicide means |
| US3901936A (en) * | 1966-10-15 | 1975-08-26 | Schering Ag | Process for the preparation of n-carbamoyloxyphenyl carbamates |
| DE2413933A1 (de) * | 1974-03-20 | 1975-09-25 | Schering Ag | Diurethane mit selektiver herbizider wirkung |
| JPS5140073A (ja) * | 1974-06-28 | 1976-04-03 | Siemens Ag | Shirikonnodoopinguhoho |
| DE2557552C2 (de) * | 1975-12-18 | 1984-12-20 | Schering AG, 1000 Berlin und 4709 Bergkamen | Diurethane und herbizide Mittel, enthaltend diese Verbindungen als Wirkstoffe |
| DE2638897C2 (de) | 1976-08-28 | 1978-10-26 | Basf Ag, 6700 Ludwigshafen | Diurethane und diese enthaltende Herbizide |
| DE2650796A1 (de) * | 1976-11-03 | 1978-05-11 | Schering Ag | Diurethane, verfahren zur herstellung dieser verbindungen sowie diese enthaltendes selektives herbizides mittel |
-
1979
- 1979-01-15 DE DE19792901658 patent/DE2901658A1/de not_active Withdrawn
- 1979-12-24 IN IN940/DEL/79A patent/IN153545B/en unknown
- 1979-12-28 FI FI794081A patent/FI794081A7/fi not_active Application Discontinuation
-
1980
- 1980-01-03 YU YU00011/80A patent/YU1180A/xx unknown
- 1980-01-08 NL NL8000112A patent/NL8000112A/nl not_active Application Discontinuation
- 1980-01-10 TR TR20529A patent/TR20529A/xx unknown
- 1980-01-11 DD DD80218424A patent/DD148709A5/de unknown
- 1980-01-11 SU SU802867755A patent/SU942587A3/ru active
- 1980-01-11 AT AT0013980A patent/AT365411B/de not_active IP Right Cessation
- 1980-01-11 PH PH23505A patent/PH15195A/en unknown
- 1980-01-11 MX MX808584U patent/MX5743E/es unknown
- 1980-01-12 EG EG21/80A patent/EG14116A/xx active
- 1980-01-14 MA MA18899A patent/MA18702A1/fr unknown
- 1980-01-14 SE SE8000278A patent/SE8000278L/xx not_active Application Discontinuation
- 1980-01-14 PT PT70692A patent/PT70692A/pt unknown
- 1980-01-14 RO RO8099869A patent/RO79454A/ro unknown
- 1980-01-14 BG BG046234A patent/BG31495A3/xx unknown
- 1980-01-14 IL IL59126A patent/IL59126A/xx unknown
- 1980-01-14 IT IT19194/80A patent/IT1130864B/it active
- 1980-01-14 GR GR60957A patent/GR71679B/el unknown
- 1980-01-14 PL PL1980221361A patent/PL125248B1/pl unknown
- 1980-01-14 CA CA343,600A patent/CA1128061A/en not_active Expired
- 1980-01-14 BG BG046235A patent/BG31465A3/xx unknown
- 1980-01-14 HU HU8063A patent/HU181682B/hu unknown
- 1980-01-15 ES ES487720A patent/ES487720A1/es not_active Expired
- 1980-01-15 FR FR8000793A patent/FR2446275A1/fr active Granted
- 1980-01-15 CH CH32280A patent/CH645343A5/de not_active IP Right Cessation
- 1980-01-15 DK DK16380A patent/DK16380A/da not_active Application Discontinuation
- 1980-01-15 GB GB8001303A patent/GB2040939B/en not_active Expired
- 1980-01-15 AR AR279638A patent/AR224143A1/es active
- 1980-01-15 ZA ZA00800244A patent/ZA80244B/xx unknown
- 1980-01-15 CS CS80312A patent/CS212336B2/cs unknown
- 1980-01-15 BE BE0/198971A patent/BE881152A/fr not_active IP Right Cessation
- 1980-01-15 AU AU54604/80A patent/AU532736B2/en not_active Ceased
- 1980-01-16 JP JP55002672A patent/JPS5823865B2/ja not_active Expired
- 1980-09-10 BR BR8000161A patent/BR8000161A/pt unknown
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