CS197327B2 - Herbicide means and method of making the active agent thereof - Google Patents
Herbicide means and method of making the active agent thereof Download PDFInfo
- Publication number
- CS197327B2 CS197327B2 CS784789A CS478978A CS197327B2 CS 197327 B2 CS197327 B2 CS 197327B2 CS 784789 A CS784789 A CS 784789A CS 478978 A CS478978 A CS 478978A CS 197327 B2 CS197327 B2 CS 197327B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- phenyl
- ester
- acid
- methylcarbanilic
- carbanilic
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 5
- 239000013543 active substance Substances 0.000 title description 5
- 238000004519 manufacturing process Methods 0.000 title description 3
- 239000004009 herbicide Substances 0.000 title description 2
- 150000001875 compounds Chemical group 0.000 claims abstract description 35
- 239000000203 mixture Substances 0.000 claims abstract description 9
- 125000003545 alkoxy group Chemical group 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
- 229910052717 sulfur Chemical group 0.000 claims abstract description 3
- -1 methoxyethyl Chemical group 0.000 claims description 98
- 239000002253 acid Substances 0.000 claims description 34
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- 239000004480 active ingredient Substances 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 6
- 239000000969 carrier Substances 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 125000004848 alkoxyethyl group Chemical group 0.000 claims description 2
- 150000007529 inorganic bases Chemical class 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 150000007530 organic bases Chemical class 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 2
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 abstract description 13
- 229920000742 Cotton Polymers 0.000 abstract description 3
- 244000000626 Daucus carota Species 0.000 abstract description 3
- 235000002767 Daucus carota Nutrition 0.000 abstract description 3
- 240000007594 Oryza sativa Species 0.000 abstract description 3
- 235000007164 Oryza sativa Nutrition 0.000 abstract description 3
- 244000061456 Solanum tuberosum Species 0.000 abstract description 3
- 235000002595 Solanum tuberosum Nutrition 0.000 abstract description 3
- 125000000217 alkyl group Chemical group 0.000 abstract description 3
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- 244000299507 Gossypium hirsutum Species 0.000 abstract description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract description 2
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- 235000012015 potatoes Nutrition 0.000 abstract description 2
- 239000011593 sulfur Chemical group 0.000 abstract description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000006193 alkinyl group Chemical group 0.000 abstract 1
- 125000004983 dialkoxyalkyl group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 description 99
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 83
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- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 13
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- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 7
- 235000010460 mustard Nutrition 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 125000006627 ethoxycarbonylamino group Chemical group 0.000 description 6
- PYJOSHDBCVEHSA-UHFFFAOYSA-N 2,2-dimethoxyethyl(phenyl)carbamic acid Chemical compound COC(OC)CN(C(O)=O)C1=CC=CC=C1 PYJOSHDBCVEHSA-UHFFFAOYSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- ZFZPIYLWLOTMSI-UHFFFAOYSA-N 2,2-dimethoxyethyl-(3-methylphenyl)carbamic acid Chemical compound COC(CN(C(O)=O)C1=CC(=CC=C1)C)OC ZFZPIYLWLOTMSI-UHFFFAOYSA-N 0.000 description 4
- RLCNIFASNGVYMF-UHFFFAOYSA-N 2-ethoxyethyl(phenyl)carbamic acid Chemical compound CCOCCN(C(O)=O)C1=CC=CC=C1 RLCNIFASNGVYMF-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 4
- MICAYBZEKACXBX-UHFFFAOYSA-N 2,2-dimethoxyethyl-(4-methylphenyl)carbamic acid Chemical compound COC(CN(C(O)=O)C1=CC=C(C=C1)C)OC MICAYBZEKACXBX-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- KZFJVVPFVUZBJL-UHFFFAOYSA-N [3-(2-methylpropoxycarbonylamino)phenyl] N-(2-methoxyethyl)-N-(3-methylphenyl)carbamate Chemical compound CC(COC(=O)NC=1C=C(C=CC1)OC(N(C1=CC(=CC=C1)C)CCOC)=O)C KZFJVVPFVUZBJL-UHFFFAOYSA-N 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 125000006626 methoxycarbonylamino group Chemical group 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- HNAXBZUMENBWSX-UHFFFAOYSA-N (3-methylphenyl)carbamic acid Chemical compound CC1=CC=CC(NC(O)=O)=C1 HNAXBZUMENBWSX-UHFFFAOYSA-N 0.000 description 2
- LLROXYDGYRPLFN-UHFFFAOYSA-N 2,2-diethoxyethyl(phenyl)carbamic acid Chemical compound C(C)OC(CN(C(O)=O)C1=CC=CC=C1)OCC LLROXYDGYRPLFN-UHFFFAOYSA-N 0.000 description 2
- DRQLZONZZZAUPR-UHFFFAOYSA-N 2-butoxyethyl(phenyl)carbamic acid Chemical compound C(CCC)OCCN(C(O)=O)C1=CC=CC=C1 DRQLZONZZZAUPR-UHFFFAOYSA-N 0.000 description 2
- ZLFMEZDAVMJTQX-UHFFFAOYSA-N 2-butoxyethyl-(3-methylphenyl)carbamic acid Chemical compound C(CCC)OCCN(C(O)=O)C1=CC(=CC=C1)C ZLFMEZDAVMJTQX-UHFFFAOYSA-N 0.000 description 2
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 2
- KLOCQEAEAAXJPF-UHFFFAOYSA-N 2-ethoxyethyl-(3-methylphenyl)carbamic acid Chemical compound C(C)OCCN(C(O)=O)C1=CC(=CC=C1)C KLOCQEAEAAXJPF-UHFFFAOYSA-N 0.000 description 2
- JKTUWYNLJVOQIV-UHFFFAOYSA-N 2-ethoxyethyl-(4-methylphenyl)carbamic acid Chemical compound C(C)OCCN(C(O)=O)C1=CC=C(C=C1)C JKTUWYNLJVOQIV-UHFFFAOYSA-N 0.000 description 2
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- RWGUGNOAHOFXBV-UHFFFAOYSA-N [3-(propan-2-yloxycarbonylamino)phenyl] N-(3-methylphenyl)-N-(2-propoxyethyl)carbamate Chemical compound CC(C)OC(=O)NC=1C=C(C=CC1)OC(N(C1=CC(=CC=C1)C)CCOCCC)=O RWGUGNOAHOFXBV-UHFFFAOYSA-N 0.000 description 1
- LJCVIOUSRZIIRF-UHFFFAOYSA-N [3-(propan-2-yloxycarbonylamino)phenyl] N-(4-methylphenyl)-N-(2-propoxyethyl)carbamate Chemical compound CC(C)OC(=O)NC=1C=C(C=CC1)OC(N(C1=CC=C(C=C1)C)CCOCCC)=O LJCVIOUSRZIIRF-UHFFFAOYSA-N 0.000 description 1
- GUUNZWXDMOKFEY-UHFFFAOYSA-N [3-(propan-2-yloxycarbonylamino)phenyl] N-phenyl-N-(2-propoxyethyl)carbamate Chemical compound CC(C)OC(=O)NC=1C=C(C=CC1)OC(N(C1=CC=CC=C1)CCOCCC)=O GUUNZWXDMOKFEY-UHFFFAOYSA-N 0.000 description 1
- RMLROPAOXLMMOK-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(2,2-diethoxyethyl)-N-phenylcarbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C1=CC=CC=C1)CC(OCC)OCC)=O RMLROPAOXLMMOK-UHFFFAOYSA-N 0.000 description 1
- BBSFTVACHSZPRM-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(2,2-dimethoxyethyl)-N-(4-methylphenyl)carbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C1=CC=C(C=C1)C)CC(OC)OC)=O BBSFTVACHSZPRM-UHFFFAOYSA-N 0.000 description 1
- LBCYBDXFDLYHLU-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(2,2-dimethoxyethyl)-N-phenylcarbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C1=CC=CC=C1)CC(OC)OC)=O LBCYBDXFDLYHLU-UHFFFAOYSA-N 0.000 description 1
- YICHVUSZVXAHFH-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(2-butoxyethyl)-N-(4-methylphenyl)carbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C1=CC=C(C=C1)C)CCOCCCC)=O YICHVUSZVXAHFH-UHFFFAOYSA-N 0.000 description 1
- TYSKSAZXMXVKAZ-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(2-ethoxyethyl)-N-(2-methylphenyl)carbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C1=C(C=CC=C1)C)CCOCC)=O TYSKSAZXMXVKAZ-UHFFFAOYSA-N 0.000 description 1
- ZNBJTCOSBRDHSP-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(2-ethoxyethyl)-N-(4-methylphenyl)carbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C1=CC=C(C=C1)C)CCOCC)=O ZNBJTCOSBRDHSP-UHFFFAOYSA-N 0.000 description 1
- IMPNGWUBOLIZPM-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(2-ethoxyethyl)-N-phenylcarbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C1=CC=CC=C1)CCOCC)=O IMPNGWUBOLIZPM-UHFFFAOYSA-N 0.000 description 1
- KHKQGXDPZMBBCC-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(2-methoxyethyl)-N-(2-methylphenyl)carbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C1=C(C=CC=C1)C)CCOC)=O KHKQGXDPZMBBCC-UHFFFAOYSA-N 0.000 description 1
- OJHLXHVVLUZZDP-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(2-methoxyethyl)-N-(3-methoxyphenyl)carbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C1=CC(=CC=C1)OC)CCOC)=O OJHLXHVVLUZZDP-UHFFFAOYSA-N 0.000 description 1
- CZCZNORGJCPKOM-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(2-methoxyethyl)-N-(3-methylphenyl)carbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C1=CC(=CC=C1)C)CCOC)=O CZCZNORGJCPKOM-UHFFFAOYSA-N 0.000 description 1
- XTBBEAFAJCXUAC-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(3-methylphenyl)-N-(2-propoxyethyl)carbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C1=CC(=CC=C1)C)CCOCCC)=O XTBBEAFAJCXUAC-UHFFFAOYSA-N 0.000 description 1
- STGRLTSVECDUET-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-phenyl-N-(2-propoxyethyl)carbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C1=CC=CC=C1)CCOCCC)=O STGRLTSVECDUET-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- BUSBFZWLPXDYIC-UHFFFAOYSA-N arsonic acid Chemical class O[AsH](O)=O BUSBFZWLPXDYIC-UHFFFAOYSA-N 0.000 description 1
- 150000008107 benzenesulfonic acids Chemical class 0.000 description 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
- 150000005130 benzoxazines Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 125000006630 butoxycarbonylamino group Chemical group 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- QQSGDKKFXBGYON-UHFFFAOYSA-N ethoxy-methylperoxy-(6-methyl-2-propan-2-ylpyrimidin-4-yl)oxy-sulfanylidene-$l^{5}-phosphane Chemical class CCOP(=S)(OOC)OC1=CC(C)=NC(C(C)C)=N1 QQSGDKKFXBGYON-UHFFFAOYSA-N 0.000 description 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 150000001469 hydantoins Chemical class 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 125000006629 isopropoxycarbonylamino group Chemical group 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
- 150000002576 ketones Chemical class 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
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 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
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- QNMLMAVEXUCXRG-UHFFFAOYSA-N oxadiazinane-4,5-dione Chemical class O=C1CONNC1=O QNMLMAVEXUCXRG-UHFFFAOYSA-N 0.000 description 1
- SDRLFDJOSQLRPB-UHFFFAOYSA-N oxadiazine-4,5-dione Chemical class O=C1CON=NC1=O SDRLFDJOSQLRPB-UHFFFAOYSA-N 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- YDCVQGAUCOROHB-UHFFFAOYSA-N oxadiazolidine-4,5-dione Chemical class O=C1NNOC1=O YDCVQGAUCOROHB-UHFFFAOYSA-N 0.000 description 1
- 210000002741 palatine tonsil Anatomy 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- REJGOFYVRVIODZ-UHFFFAOYSA-N phosphanium;chloride Chemical class P.Cl REJGOFYVRVIODZ-UHFFFAOYSA-N 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 150000003053 piperidines Chemical class 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- BFZYLUGEHGYJKJ-UHFFFAOYSA-N pyrazolidine-3-thione Chemical class S=C1CCNN1 BFZYLUGEHGYJKJ-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 150000005299 pyridinones Chemical class 0.000 description 1
- 150000008318 pyrimidones Chemical class 0.000 description 1
- NYCVCXMSZNOGDH-UHFFFAOYSA-N pyrrolidine-1-carboxylic acid Chemical class OC(=O)N1CCCC1 NYCVCXMSZNOGDH-UHFFFAOYSA-N 0.000 description 1
- 150000003235 pyrrolidines Chemical class 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 150000003254 radicals Chemical class 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
- 239000002002 slurry Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000003011 styrenyl group Chemical class [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 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
- 150000003566 thiocarboxylic acids Chemical class 0.000 description 1
- 150000003582 thiophosphoric acids Chemical class 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 239000008096 xylene Substances 0.000 description 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
Landscapes
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772732848 DE2732848A1 (de) | 1977-07-18 | 1977-07-18 | Diurethane, herbizide mittel enthaltend diese verbindungen sowie verfahren zu ihrer herstellung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS197327B2 true CS197327B2 (en) | 1980-04-30 |
Family
ID=6014434
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS784789A CS197327B2 (en) | 1977-07-18 | 1978-07-18 | Herbicide means and method of making the active agent thereof |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US4441915A (pl) |
| JP (1) | JPS5422340A (pl) |
| AU (1) | AU519399B2 (pl) |
| BE (1) | BE869074A (pl) |
| CA (1) | CA1103268A (pl) |
| CH (1) | CH637372A5 (pl) |
| CS (1) | CS197327B2 (pl) |
| DD (1) | DD137822A5 (pl) |
| DE (1) | DE2732848A1 (pl) |
| DK (1) | DK320778A (pl) |
| ES (1) | ES471736A1 (pl) |
| FR (1) | FR2398053A1 (pl) |
| GB (1) | GB2002356B (pl) |
| GR (1) | GR73026B (pl) |
| HU (1) | HU180531B (pl) |
| IE (1) | IE47234B1 (pl) |
| IL (1) | IL55156A (pl) |
| IT (1) | IT1097530B (pl) |
| LU (1) | LU79980A1 (pl) |
| NL (1) | NL7807482A (pl) |
| PL (1) | PL111138B1 (pl) |
| PT (1) | PT68309A (pl) |
| SU (2) | SU717990A3 (pl) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU187288B (en) * | 1980-04-28 | 1985-12-28 | Stauffer Chemical Co | Synergetic herbicide compositions |
| GR78909B (pl) * | 1982-08-13 | 1984-10-02 | Sipcam Spa | |
| US6150328A (en) * | 1986-07-01 | 2000-11-21 | Genetics Institute, Inc. | BMP products |
| ATE238417T1 (de) * | 1991-11-04 | 2003-05-15 | Inst Genetics Llc | Rekombinante knochenmorphogenetische protein heterodimere, zusammensetzungen und verfahren zur verwendung |
| US20080139474A1 (en) * | 1991-11-04 | 2008-06-12 | David Israel | Recombinant bone morphogenetic protein heterodimers, compositions and methods of use |
| US6291206B1 (en) * | 1993-09-17 | 2001-09-18 | Genetics Institute, Inc. | BMP receptor proteins |
| ATE319823T1 (de) | 1993-12-07 | 2006-03-15 | Inst Genetics Llc | Bmp-12, bmp-13 und diese enthaltende sehne- induzierende zusammensetzungen |
| US6727224B1 (en) * | 1999-02-01 | 2004-04-27 | Genetics Institute, Llc. | Methods and compositions for healing and repair of articular cartilage |
| DK1223990T3 (da) | 1999-10-15 | 2004-11-29 | Inst Genetics Llc | Formuleringer af hyaluronsyre til tilförsel af osteogene proteiner |
| US20030082233A1 (en) * | 2000-12-01 | 2003-05-01 | Lyons Karen M. | Method and composition for modulating bone growth |
| EP1399023B1 (en) * | 2001-06-01 | 2008-04-30 | Wyeth | COMPOSITIONS FOR SYSTEMIC ADMINISTRATION OF SEQUENCES ENCODING BONE MORPHOGENETIC PROTEINS& x9; |
| TWI267378B (en) * | 2001-06-08 | 2006-12-01 | Wyeth Corp | Calcium phosphate delivery vehicles for osteoinductive proteins |
| JP4879482B2 (ja) * | 2002-05-17 | 2012-02-22 | ワイス・エルエルシー | 骨原性タンパク質を送達するための注入可能な固体ヒアルロン酸キャリア |
| CN101897974B (zh) * | 2003-09-12 | 2013-09-25 | 惠氏公司 | 用于递送成骨蛋白的注射型磷酸钙固体小棒剂和糊剂 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3133808A (en) * | 1959-03-16 | 1964-05-19 | Monsanto Chemicals | Herbicide composition |
| US3404975A (en) * | 1964-12-18 | 1968-10-08 | Fmc Corp | m-(carbamoyloxy)-carbanilates as herbicides |
| 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 |
| US3551477A (en) * | 1966-07-06 | 1970-12-29 | Basf Ag | Novel biscarbamates |
| US3901936A (en) * | 1966-10-15 | 1975-08-26 | Schering Ag | Process for the preparation of n-carbamoyloxyphenyl carbamates |
| US3865867A (en) * | 1967-06-19 | 1975-02-11 | Monsanto Co | Meta-bifunctional benzenes |
| DE2108975C3 (de) * | 1971-02-16 | 1979-12-20 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | N-Acyl-Diurethane sowie diese enthaltendes herbizides Mittel |
| EG10699A (en) * | 1971-06-23 | 1976-07-31 | Bayer Ag | Novel n.carbamic aryl acid esters method for preparation and their use for controlling plant growth |
| US4022611A (en) * | 1972-06-06 | 1977-05-10 | Ciba-Geigy Corporation | Plant growth regulating agent |
| US3997325A (en) * | 1973-05-24 | 1976-12-14 | American Cyanamid Company | (Alkynyloxy)alkyl and (alkenyloxy)alkyl carbamates and their use as herbicides |
| US3976470A (en) * | 1975-07-23 | 1976-08-24 | Stauffer Chemical Company | Diphenyl ether amides |
-
1977
- 1977-07-18 DE DE19772732848 patent/DE2732848A1/de not_active Withdrawn
-
1978
- 1978-07-03 SU SU782632100A patent/SU717990A3/ru active
- 1978-07-11 NL NL7807482A patent/NL7807482A/xx not_active Application Discontinuation
- 1978-07-12 SU SU782633658A patent/SU858561A3/ru active
- 1978-07-12 CA CA307,243A patent/CA1103268A/en not_active Expired
- 1978-07-14 ES ES471736A patent/ES471736A1/es not_active Expired
- 1978-07-14 GR GR56776A patent/GR73026B/el unknown
- 1978-07-14 LU LU79980A patent/LU79980A1/xx unknown
- 1978-07-14 DD DD78206729A patent/DD137822A5/xx unknown
- 1978-07-14 CH CH766978A patent/CH637372A5/de not_active IP Right Cessation
- 1978-07-15 PL PL1978208435A patent/PL111138B1/pl unknown
- 1978-07-17 PT PT68309A patent/PT68309A/pt unknown
- 1978-07-17 GB GB7830049A patent/GB2002356B/en not_active Expired
- 1978-07-17 IE IE1440/78A patent/IE47234B1/en unknown
- 1978-07-17 FR FR7821127A patent/FR2398053A1/fr active Granted
- 1978-07-17 HU HU78SCHE652A patent/HU180531B/hu unknown
- 1978-07-17 IT IT25741/78A patent/IT1097530B/it active
- 1978-07-17 JP JP8621978A patent/JPS5422340A/ja active Pending
- 1978-07-17 IL IL55156A patent/IL55156A/xx unknown
- 1978-07-18 CS CS784789A patent/CS197327B2/cs unknown
- 1978-07-18 DK DK320778A patent/DK320778A/da not_active Application Discontinuation
- 1978-07-18 AU AU38104/78A patent/AU519399B2/en not_active Expired
- 1978-07-18 BE BE189340A patent/BE869074A/xx not_active IP Right Cessation
-
1981
- 1981-07-15 US US06/283,661 patent/US4441915A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| GB2002356A (en) | 1979-02-21 |
| FR2398053B1 (pl) | 1982-11-19 |
| FR2398053A1 (fr) | 1979-02-16 |
| SU717990A3 (ru) | 1980-02-25 |
| AU3810478A (en) | 1980-01-24 |
| LU79980A1 (pl) | 1978-12-12 |
| IT7825741A0 (it) | 1978-07-17 |
| CH637372A5 (de) | 1983-07-29 |
| IL55156A0 (en) | 1978-09-29 |
| CA1103268A (en) | 1981-06-16 |
| DE2732848A1 (de) | 1979-02-08 |
| PT68309A (de) | 1978-08-01 |
| PL208435A1 (pl) | 1979-03-26 |
| GR73026B (pl) | 1984-01-25 |
| IL55156A (en) | 1982-11-30 |
| DK320778A (da) | 1979-01-19 |
| NL7807482A (nl) | 1979-01-22 |
| JPS5422340A (en) | 1979-02-20 |
| IE47234B1 (en) | 1984-01-25 |
| IE781440L (en) | 1979-01-18 |
| SU858561A3 (ru) | 1981-08-23 |
| GB2002356B (en) | 1982-03-03 |
| AU519399B2 (en) | 1981-12-03 |
| HU180531B (en) | 1983-03-28 |
| PL111138B1 (en) | 1980-08-30 |
| ES471736A1 (es) | 1979-02-01 |
| BE869074A (fr) | 1979-01-18 |
| IT1097530B (it) | 1985-08-31 |
| US4441915A (en) | 1984-04-10 |
| DD137822A5 (de) | 1979-09-26 |
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