TW213447B - - Google Patents

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Publication number: TW213447B
Authority: TW; Taiwan
Prior art keywords: cis; methyl; acid; butene; group
Prior art date: 1991-08-15

Application number

TW80107669A

Other languages

English (en)

Chinese (zh)

Original Assignee

Rohm & Haas

Priority date (The priority date 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 date listed.)

1991-08-15

Filing date

1991-09-27

Publication date

1993-09-21

1991-09-27 Application filed by Rohm & Haas filed Critical Rohm & Haas

1993-09-21 Application granted granted Critical

1993-09-21 Publication of TW213447B publication Critical patent/TW213447B/zh

Links

150000001875 compounds Chemical class 0.000 claims description 66
-1 cis-3-thiocyanoacrylic acid phenyl ester Chemical class 0.000 claims description 40
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 32
239000000203 mixture Substances 0.000 claims description 26
239000007789 gas Substances 0.000 claims description 18
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
239000000126 substance Substances 0.000 claims description 15
238000000034 method Methods 0.000 claims description 14
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
239000002253 acid Substances 0.000 claims description 13
125000000217 alkyl group Chemical group 0.000 claims description 12
229910052739 hydrogen Inorganic materials 0.000 claims description 12
229910052717 sulfur Inorganic materials 0.000 claims description 11
239000011593 sulfur Substances 0.000 claims description 11
239000001257 hydrogen Substances 0.000 claims description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
OQYPGQSDSUQZBM-UPHRSURJSA-N (z)-3-thiocyanatoprop-2-enoic acid Chemical compound OC(=O)\C=C/SC#N OQYPGQSDSUQZBM-UPHRSURJSA-N 0.000 claims description 7
229910052736 halogen Inorganic materials 0.000 claims description 7
150000002367 halogens Chemical group 0.000 claims description 7
125000001424 substituent group Chemical group 0.000 claims description 7
125000003943 azolyl group Chemical group 0.000 claims description 6
230000012010 growth Effects 0.000 claims description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 5
241000894007 species Species 0.000 claims description 5
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 4
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 4
125000000232 haloalkynyl group Chemical group 0.000 claims description 4
229910052757 nitrogen Inorganic materials 0.000 claims description 4
HNUKTDKISXPDPA-UHFFFAOYSA-N 2-oxopropyl Chemical compound [CH2]C(C)=O HNUKTDKISXPDPA-UHFFFAOYSA-N 0.000 claims description 3
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 3
150000001335 aliphatic alkanes Chemical class 0.000 claims description 3
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
150000003839 salts Chemical class 0.000 claims description 3
239000012298 atmosphere Substances 0.000 claims description 2
239000001273 butane Substances 0.000 claims description 2
150000004702 methyl esters Chemical class 0.000 claims description 2
UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 13
ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 claims 2
125000001412 tetrahydropyranyl group Chemical group 0.000 claims 2
URIOHGXETKQAEG-UHFFFAOYSA-N (3-methylphenyl)methyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CC(C)=C1 URIOHGXETKQAEG-UHFFFAOYSA-N 0.000 claims 1
QWGSYBNGJXNFOO-UHFFFAOYSA-N (3-oxo-1-phenylbut-1-enyl) thiocyanate Chemical compound CC(=O)C=C(SC#N)C1=CC=CC=C1 QWGSYBNGJXNFOO-UHFFFAOYSA-N 0.000 claims 1
BUZYGTVTZYSBCU-UHFFFAOYSA-N 1-(4-chlorophenyl)ethanone Chemical compound CC(=O)C1=CC=C(Cl)C=C1 BUZYGTVTZYSBCU-UHFFFAOYSA-N 0.000 claims 1
FEUFEGJTJIHPOF-UHFFFAOYSA-N 2-butyl acrylic acid Chemical compound CCCCC(=C)C(O)=O FEUFEGJTJIHPOF-UHFFFAOYSA-N 0.000 claims 1
IJVRPNIWWODHHA-UHFFFAOYSA-N 2-cyanoprop-2-enoic acid Chemical compound OC(=O)C(=C)C#N IJVRPNIWWODHHA-UHFFFAOYSA-N 0.000 claims 1
125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
239000005711 Benzoic acid Substances 0.000 claims 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 1
CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 claims 1
241000282994 Cervidae Species 0.000 claims 1
229920001651 Cyanoacrylate Polymers 0.000 claims 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 claims 1
239000008186 active pharmaceutical agent Substances 0.000 claims 1
125000003545 alkoxy group Chemical group 0.000 claims 1
229960004050 aminobenzoic acid Drugs 0.000 claims 1
235000010233 benzoic acid Nutrition 0.000 claims 1
229910052797 bismuth Inorganic materials 0.000 claims 1
JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims 1
FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 claims 1
229910052802 copper Inorganic materials 0.000 claims 1
239000010949 copper Substances 0.000 claims 1
229940053009 ethyl cyanoacrylate Drugs 0.000 claims 1
230000009545 invasion Effects 0.000 claims 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 1
125000002971 oxazolyl group Chemical group 0.000 claims 1
WHMDPDGBKYUEMW-UHFFFAOYSA-N pyridine-2-thiol Chemical group SC1=CC=CC=N1 WHMDPDGBKYUEMW-UHFFFAOYSA-N 0.000 claims 1
125000004076 pyridyl group Chemical group 0.000 claims 1
229910052714 tellurium Inorganic materials 0.000 claims 1
ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical group [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims 1
235000013311 vegetables Nutrition 0.000 claims 1
239000000243 solution Substances 0.000 description 39
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 34
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 33
239000000123 paper Substances 0.000 description 30
238000012360 testing method Methods 0.000 description 29
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 28
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 27
239000003795 chemical substances by application Substances 0.000 description 26
239000000047 product Substances 0.000 description 21
239000003921 oil Substances 0.000 description 17
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 16
238000005406 washing Methods 0.000 description 16
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
239000000463 material Substances 0.000 description 14
239000007787 solid Substances 0.000 description 14
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
241000894006 Bacteria Species 0.000 description 11
241000196324 Embryophyta Species 0.000 description 11
239000000725 suspension Substances 0.000 description 11
241000209140 Triticum Species 0.000 description 10
235000021307 Triticum Nutrition 0.000 description 10
239000004744 fabric Substances 0.000 description 10
239000007788 liquid Substances 0.000 description 10
239000002023 wood Substances 0.000 description 10
235000013882 gravy Nutrition 0.000 description 9
239000004753 textile Substances 0.000 description 9
241000233866 Fungi Species 0.000 description 8
230000003115 biocidal effect Effects 0.000 description 8
229940125782 compound 2 Drugs 0.000 description 8
235000013305 food Nutrition 0.000 description 8
239000000344 soap Substances 0.000 description 8
239000007864 aqueous solution Substances 0.000 description 7
238000011081 inoculation Methods 0.000 description 7
239000000314 lubricant Substances 0.000 description 7
229910052943 magnesium sulfate Inorganic materials 0.000 description 7
239000002609 medium Substances 0.000 description 7
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 6
241000195493 Cryptophyta Species 0.000 description 6
241000589517 Pseudomonas aeruginosa Species 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
125000003710 aryl alkyl group Chemical group 0.000 description 6
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
201000010099 disease Diseases 0.000 description 6
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 6
239000003814 drug Substances 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
238000002844 melting Methods 0.000 description 6
230000008018 melting Effects 0.000 description 6
241000235349 Ascomycota Species 0.000 description 5
241000223678 Aureobasidium pullulans Species 0.000 description 5
241000589540 Pseudomonas fluorescens Species 0.000 description 5
241000233639 Pythium Species 0.000 description 5
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
241000191967 Staphylococcus aureus Species 0.000 description 5
239000003242 anti bacterial agent Substances 0.000 description 5
239000003139 biocide Substances 0.000 description 5
230000008030 elimination Effects 0.000 description 5
238000003379 elimination reaction Methods 0.000 description 5
238000011049 filling Methods 0.000 description 5
239000000446 fuel Substances 0.000 description 5
238000004519 manufacturing process Methods 0.000 description 5
238000007639 printing Methods 0.000 description 5
238000012545 processing Methods 0.000 description 5
238000003860 storage Methods 0.000 description 5
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
NLZOTBCJKRTNDJ-IHWYPQMZSA-N [(z)-3-oxobut-1-enyl] thiocyanate Chemical compound CC(=O)\C=C/SC#N NLZOTBCJKRTNDJ-IHWYPQMZSA-N 0.000 description 4
239000000853 adhesive Substances 0.000 description 4
230000001070 adhesive effect Effects 0.000 description 4
125000000304 alkynyl group Chemical group 0.000 description 4
SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 4
230000000844 anti-bacterial effect Effects 0.000 description 4
239000003124 biologic agent Substances 0.000 description 4
238000005260 corrosion Methods 0.000 description 4
239000013078 crystal Substances 0.000 description 4
238000001035 drying Methods 0.000 description 4
239000003480 eluent Substances 0.000 description 4
230000032050 esterification Effects 0.000 description 4
238000005886 esterification reaction Methods 0.000 description 4
230000000855 fungicidal effect Effects 0.000 description 4
239000010985 leather Substances 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
239000003973 paint Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000007921 spray Substances 0.000 description 4
UAOUIVVJBYDFKD-XKCDOFEDSA-N (1R,9R,10S,11R,12R,15S,18S,21R)-10,11,21-trihydroxy-8,8-dimethyl-14-methylidene-4-(prop-2-enylamino)-20-oxa-5-thia-3-azahexacyclo[9.7.2.112,15.01,9.02,6.012,18]henicosa-2(6),3-dien-13-one Chemical compound C([C@@H]1[C@@H](O)[C@@]23C(C1=C)=O)C[C@H]2[C@]12C(N=C(NCC=C)S4)=C4CC(C)(C)[C@H]1[C@H](O)[C@]3(O)OC2 UAOUIVVJBYDFKD-XKCDOFEDSA-N 0.000 description 3
IWZSHWBGHQBIML-ZGGLMWTQSA-N (3S,8S,10R,13S,14S,17S)-17-isoquinolin-7-yl-N,N,10,13-tetramethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-amine Chemical compound CN(C)[C@H]1CC[C@]2(C)C3CC[C@@]4(C)[C@@H](CC[C@@H]4c4ccc5ccncc5c4)[C@@H]3CC=C2C1 IWZSHWBGHQBIML-ZGGLMWTQSA-N 0.000 description 3
UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
241000588724 Escherichia coli Species 0.000 description 3
241000223218 Fusarium Species 0.000 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 description 3
241001465754 Metazoa Species 0.000 description 3
241000233616 Phytophthora capsici Species 0.000 description 3
240000004808 Saccharomyces cerevisiae Species 0.000 description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical class [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 3
WREOTYWODABZMH-DTZQCDIJSA-N [[(2r,3s,4r,5r)-3,4-dihydroxy-5-[2-oxo-4-(2-phenylethoxyamino)pyrimidin-1-yl]oxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate Chemical compound O[C@@H]1[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O[C@H]1N(C=C\1)C(=O)NC/1=N\OCCC1=CC=CC=C1 WREOTYWODABZMH-DTZQCDIJSA-N 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
229940088710 antibiotic agent Drugs 0.000 description 3
XRGPFNGLRSIPSA-UHFFFAOYSA-N butyn-2-one Chemical compound CC(=O)C#C XRGPFNGLRSIPSA-UHFFFAOYSA-N 0.000 description 3
229940125758 compound 15 Drugs 0.000 description 3
239000000498 cooling water Substances 0.000 description 3
230000006378 damage Effects 0.000 description 3
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150000002148 esters Chemical class 0.000 description 3
238000011156 evaluation Methods 0.000 description 3
238000000855 fermentation Methods 0.000 description 3
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239000001963 growth medium Substances 0.000 description 3
238000000338 in vitro Methods 0.000 description 3
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239000007924 injection Substances 0.000 description 3
239000010410 layer Substances 0.000 description 3
239000008267 milk Substances 0.000 description 3
238000004321 preservation Methods 0.000 description 3
229910052704 radon Inorganic materials 0.000 description 3
SYUHGPGVQRZVTB-UHFFFAOYSA-N radon atom Chemical compound [Rn] SYUHGPGVQRZVTB-UHFFFAOYSA-N 0.000 description 3
238000010898 silica gel chromatography Methods 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
238000009987 spinning Methods 0.000 description 3
239000003053 toxin Substances 0.000 description 3
231100000765 toxin Toxicity 0.000 description 3
ABJSOROVZZKJGI-OCYUSGCXSA-N (1r,2r,4r)-2-(4-bromophenyl)-n-[(4-chlorophenyl)-(2-fluoropyridin-4-yl)methyl]-4-morpholin-4-ylcyclohexane-1-carboxamide Chemical compound C1=NC(F)=CC(C(NC(=O)[C@H]2[C@@H](C[C@@H](CC2)N2CCOCC2)C=2C=CC(Br)=CC=2)C=2C=CC(Cl)=CC=2)=C1 ABJSOROVZZKJGI-OCYUSGCXSA-N 0.000 description 2
WWTBZEKOSBFBEM-SPWPXUSOSA-N (2s)-2-[[2-benzyl-3-[hydroxy-[(1r)-2-phenyl-1-(phenylmethoxycarbonylamino)ethyl]phosphoryl]propanoyl]amino]-3-(1h-indol-3-yl)propanoic acid Chemical compound N([C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)O)C(=O)C(CP(O)(=O)[C@H](CC=1C=CC=CC=1)NC(=O)OCC=1C=CC=CC=1)CC1=CC=CC=C1 WWTBZEKOSBFBEM-SPWPXUSOSA-N 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 2
229920001817 Agar Polymers 0.000 description 2
241000228245 Aspergillus niger Species 0.000 description 2
102000040350 B family Human genes 0.000 description 2
108091072128 B family Proteins 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
238000005684 Liebig rearrangement reaction Methods 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
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
241000233654 Oomycetes Species 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
241000813090 Rhizoctonia solani Species 0.000 description 2
241000700605 Viruses Species 0.000 description 2
241000589636 Xanthomonas campestris Species 0.000 description 2
125000002252 acyl group Chemical group 0.000 description 2
239000008272 agar Substances 0.000 description 2
125000003282 alkyl amino group Chemical group 0.000 description 2
150000001412 amines Chemical group 0.000 description 2
239000004599 antimicrobial Substances 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
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XLJMAIOERFSOGZ-UHFFFAOYSA-N cyanic acid Chemical class OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 description 2
125000004093 cyano group Chemical group *C#N 0.000 description 2
239000003599 detergent Substances 0.000 description 2
125000004663 dialkyl amino group Chemical group 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
230000005611 electricity Effects 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
230000007613 environmental effect Effects 0.000 description 2
239000012259 ether extract Substances 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000012530 fluid Substances 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
239000003292 glue Substances 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
125000005842 heteroatom Chemical group 0.000 description 2
238000007689 inspection Methods 0.000 description 2
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
239000012528 membrane Substances 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
XXMBUYBSZUCZHK-NSCUHMNNSA-N methyl (e)-3-thiocyanatoprop-2-enoate Chemical compound COC(=O)\C=C\SC#N XXMBUYBSZUCZHK-NSCUHMNNSA-N 0.000 description 2
UDZQRQJTSXEJDF-UHFFFAOYSA-N methyl 3-bromo-3-thiocyanatoprop-2-enoate Chemical compound COC(=O)C=C(Br)SC#N UDZQRQJTSXEJDF-UHFFFAOYSA-N 0.000 description 2
PITMUHRRCBFULF-UHFFFAOYSA-N methyl 3-bromoprop-2-ynoate Chemical compound COC(=O)C#CBr PITMUHRRCBFULF-UHFFFAOYSA-N 0.000 description 2
210000004080 milk Anatomy 0.000 description 2
235000013336 milk Nutrition 0.000 description 2
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Agricultural Chemicals And Associated Chemicals (AREA)

TW80107669A 1991-08-15 1991-09-27 TW213447B (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US56880991A	1991-08-15	1991-08-15

Publications (1)

Publication Number	Publication Date
TW213447B true TW213447B (de)	1993-09-21

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ID=51357115

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
TW80107669A TW213447B (de)	1991-08-15	1991-09-27

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TW (1)	TW213447B (de)

1991
- 1991-09-27 TW TW80107669A patent/TW213447B/zh active

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