CS199750B2 - Agent for treatment of soil or seeds for sowing against phythopathogic microorganisms - Google Patents

Agent for treatment of soil or seeds for sowing against phythopathogic microorganisms Download PDF

Info

Publication number: CS199750B2
Authority: CS; Czechoslovakia
Prior art keywords: soil; seed; active ingredient; microorganisms; treatment
Prior art date: 1977-12-01

Application number

CS787857A

Other languages

Czech (cs)

English (en)

Inventor

Johannes Kuipers

Hendrik Dolman

Original Assignee

Philips Nv

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.)

1977-12-01

Filing date

1978-11-29

Publication date

1980-07-31

1978-11-29 Application filed by Philips Nv filed Critical Philips Nv

1980-07-31 Publication of CS199750B2 publication Critical patent/CS199750B2/cs

Links

239000002689 soil Substances 0.000 title claims abstract description 24
244000005700 microbiome Species 0.000 title claims abstract description 10
238000009331 sowing Methods 0.000 title abstract description 4
239000003795 chemical substances by application Substances 0.000 title 1
239000000203 mixture Substances 0.000 claims abstract description 42
DTFCQYJITNKKDZ-UHFFFAOYSA-N 5-nitro-1,3-thiazole-2-carbonitrile Chemical compound [O-][N+](=O)C1=CN=C(C#N)S1 DTFCQYJITNKKDZ-UHFFFAOYSA-N 0.000 claims abstract description 13
239000004480 active ingredient Substances 0.000 claims description 20
239000007788 liquid Substances 0.000 claims description 7
230000003032 phytopathogenic effect Effects 0.000 claims description 5
239000007787 solid Substances 0.000 claims description 5
239000013543 active substance Substances 0.000 abstract description 7
208000015181 infectious disease Diseases 0.000 abstract description 2
241000196324 Embryophyta Species 0.000 description 12
238000009472 formulation Methods 0.000 description 12
150000001875 compounds Chemical class 0.000 description 10
241000233639 Pythium Species 0.000 description 8
-1 chalk Chemical compound 0.000 description 8
239000008187 granular material Substances 0.000 description 8
239000003921 oil Substances 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
241000209140 Triticum Species 0.000 description 6
235000021307 Triticum Nutrition 0.000 description 6
230000018109 developmental process Effects 0.000 description 6
239000000843 powder Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
235000016068 Berberis vulgaris Nutrition 0.000 description 5
241000335053 Beta vulgaris Species 0.000 description 5
240000008042 Zea mays Species 0.000 description 5
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 5
235000002017 Zea mays subsp mays Nutrition 0.000 description 5
235000005822 corn Nutrition 0.000 description 5
240000005979 Hordeum vulgare Species 0.000 description 4
235000007340 Hordeum vulgare Nutrition 0.000 description 4
201000010099 disease Diseases 0.000 description 4
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
238000002156 mixing Methods 0.000 description 4
239000005995 Aluminium silicate Substances 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
241000233866 Fungi Species 0.000 description 3
241000813090 Rhizoctonia solani Species 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
239000012876 carrier material Substances 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
239000000417 fungicide Substances 0.000 description 3
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 3
238000000034 method Methods 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
240000006240 Linum usitatissimum Species 0.000 description 2
235000004431 Linum usitatissimum Nutrition 0.000 description 2
241001459558 Monographella nivalis Species 0.000 description 2
GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
241000975369 Phoma betae Species 0.000 description 2
241000228454 Pyrenophora graminea Species 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
241000722093 Tilletia caries Species 0.000 description 2
241000514371 Ustilago avenae Species 0.000 description 2
239000000443 aerosol Substances 0.000 description 2
239000000440 bentonite Substances 0.000 description 2
229910000278 bentonite Inorganic materials 0.000 description 2
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
239000011230 binding agent Substances 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000012990 dithiocarbamate Substances 0.000 description 2
239000010459 dolomite Substances 0.000 description 2
229910000514 dolomite Inorganic materials 0.000 description 2
210000005069 ears Anatomy 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
239000003063 flame retardant Substances 0.000 description 2
230000002538 fungal effect Effects 0.000 description 2
230000000855 fungicidal effect Effects 0.000 description 2
239000001963 growth medium Substances 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
239000002917 insecticide Substances 0.000 description 2
239000000314 lubricant Substances 0.000 description 2
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
239000011707 mineral Substances 0.000 description 2
239000005645 nematicide Substances 0.000 description 2
230000000361 pesticidal effect Effects 0.000 description 2
208000024891 symptom Diseases 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
YLGFENJNDRVARS-UHFFFAOYSA-N (1-carbamoylbenzimidazol-2-yl)carbamic acid Chemical class C1=CC=C2N(C(=O)N)C(NC(O)=O)=NC2=C1 YLGFENJNDRVARS-UHFFFAOYSA-N 0.000 description 1
LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 1
WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 description 1
MHKBMNACOMRIAW-UHFFFAOYSA-N 2,3-dinitrophenol Chemical class OC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O MHKBMNACOMRIAW-UHFFFAOYSA-N 0.000 description 1
YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
QRNATDQRFAUDKF-UHFFFAOYSA-N 2-carbamothioylsulfanylethyl carbamodithioate Chemical compound NC(=S)SCCSC(N)=S QRNATDQRFAUDKF-UHFFFAOYSA-N 0.000 description 1
YAUCKEPYKXHCFF-UHFFFAOYSA-N 2-carbamothioylsulfanylethyl carbamodithioate;manganese Chemical compound [Mn].NC(=S)SCCSC(N)=S YAUCKEPYKXHCFF-UHFFFAOYSA-N 0.000 description 1
JMZRZEXRYJUHEB-UHFFFAOYSA-N 2-carbamothioylsulfanylethyl carbamodithioate;zinc Chemical compound [Zn].NC(=S)SCCSC(N)=S JMZRZEXRYJUHEB-UHFFFAOYSA-N 0.000 description 1
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 1
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 1
229920001817 Agar Polymers 0.000 description 1
235000021537 Beetroot Nutrition 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical class CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
208000004770 Fusariosis Diseases 0.000 description 1
241000223218 Fusarium Species 0.000 description 1
HRYILSDLIGTCOP-UHFFFAOYSA-N N-benzoylurea Chemical class NC(=O)NC(=O)C1=CC=CC=C1 HRYILSDLIGTCOP-UHFFFAOYSA-N 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000118205 Ovicides Species 0.000 description 1
241001503951 Phoma Species 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
229920001214 Polysorbate 60 Polymers 0.000 description 1
241000228453 Pyrenophora Species 0.000 description 1
241001361634 Rhizoctonia Species 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
241000722133 Tilletia Species 0.000 description 1
BABJTMNVJXLAEX-UHFFFAOYSA-N Triamiphos Chemical compound N1=C(N)N(P(=O)(N(C)C)N(C)C)N=C1C1=CC=CC=C1 BABJTMNVJXLAEX-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
230000002411 adverse Effects 0.000 description 1
239000008272 agar Substances 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
239000003429 antifungal agent Substances 0.000 description 1
229940121375 antifungal agent Drugs 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
235000013539 calcium stearate Nutrition 0.000 description 1
239000008116 calcium stearate Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 1
239000008119 colloidal silica Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
QQQYTWIFVNKMRW-UHFFFAOYSA-N diflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C=C1 QQQYTWIFVNKMRW-UHFFFAOYSA-N 0.000 description 1
238000007865 diluting Methods 0.000 description 1
150000004659 dithiocarbamates Chemical class 0.000 description 1
239000000428 dust Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
WDQNIWFZKXZFAY-UHFFFAOYSA-M fentin acetate Chemical compound CC([O-])=O.C1=CC=CC=C1[Sn+](C=1C=CC=CC=1)C1=CC=CC=C1 WDQNIWFZKXZFAY-UHFFFAOYSA-M 0.000 description 1
BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 1
239000000446 fuel Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
229910052602 gypsum Inorganic materials 0.000 description 1
238000003898 horticulture Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
238000011534 incubation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
235000019359 magnesium stearate Nutrition 0.000 description 1
239000000463 material Substances 0.000 description 1
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
GSNFYOQDXZLILZ-UHFFFAOYSA-N n-phenylfuran-3-carboxamide Chemical class C1=COC=C1C(=O)NC1=CC=CC=C1 GSNFYOQDXZLILZ-UHFFFAOYSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
239000001272 nitrous oxide Substances 0.000 description 1
239000004533 oil dispersion Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000003209 petroleum derivative Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000005871 repellent Substances 0.000 description 1
230000002940 repellent Effects 0.000 description 1
230000005070 ripening Effects 0.000 description 1
210000003296 saliva Anatomy 0.000 description 1
239000004576 sand Substances 0.000 description 1
238000007873 sieving Methods 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
239000000779 smoke Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
235000013599 spices Nutrition 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
239000002641 tar oil Substances 0.000 description 1
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pretreatment Of Seeds And Plants (AREA)

CS787857A 1977-12-01 1978-11-29 Agent for treatment of soil or seeds for sowing against phythopathogic microorganisms CS199750B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
NL7713267A NL7713267A (nl)	1977-12-01	1977-12-01	Preparaat voor de behandeling van grond of zaad tegen fytofage micro-organismen.

Publications (1)

Publication Number	Publication Date
CS199750B2 true CS199750B2 (en)	1980-07-31

Family

ID=19829661

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS787857A CS199750B2 (en)	1977-12-01	1978-11-29	Agent for treatment of soil or seeds for sowing against phythopathogic microorganisms

Country Status (19)

Country	Link
US (1)	US4221801A (pl)
JP (1)	JPS5513257A (pl)
AU (1)	AU4205678A (pl)
BE (1)	BE872384A (pl)
BG (1)	BG28684A3 (pl)
CS (1)	CS199750B2 (pl)
DD (1)	DD141404A5 (pl)
DE (1)	DE2851376A1 (pl)
DK (1)	DK531378A (pl)
FR (1)	FR2410435A1 (pl)
GB (1)	GB2008951A (pl)
IL (1)	IL56066A0 (pl)
IT (1)	IT1100380B (pl)
NL (1)	NL7713267A (pl)
NZ (1)	NZ189028A (pl)
PL (1)	PL211327A1 (pl)
SU (1)	SU795434A3 (pl)
TR (1)	TR19992A (pl)
ZA (1)	ZA786277B (pl)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1924830A1 (de) *	1968-07-06	1970-11-19	Merck Patent Gmbh	Neues Verfahren zur Herstellung von 5-Acylamino-isothiazolderivaten
GB1283262A (en) *	1970-04-15	1972-07-26	Lilly Industries Ltd	5-nitro-2-thiocarbamyl thiazole
US3740400A (en) *	1971-02-01	1973-06-19	American Cyanamid Co	Conversion of heteroaromatic methyl compounds to nitriles
US4006241A (en) *	1972-06-23	1977-02-01	Schering Aktiengesellschaft	Certain halothien-2-yl 5-nitrothiazol-2-yl ketones and fungicidal composition

1977
- 1977-12-01 NL NL7713267A patent/NL7713267A/xx not_active Application Discontinuation
1978
- 1978-11-07 ZA ZA786277A patent/ZA786277B/xx unknown
- 1978-11-28 IT IT30292/78A patent/IT1100380B/it active
- 1978-11-28 DK DK531378A patent/DK531378A/da unknown
- 1978-11-28 NZ NZ189028A patent/NZ189028A/xx unknown
- 1978-11-28 JP JP14615678A patent/JPS5513257A/ja active Pending
- 1978-11-28 TR TR19992A patent/TR19992A/xx unknown
- 1978-11-28 GB GB7846267A patent/GB2008951A/en not_active Withdrawn
- 1978-11-28 DE DE19782851376 patent/DE2851376A1/de not_active Withdrawn
- 1978-11-28 IL IL56066A patent/IL56066A0/xx unknown
- 1978-11-29 SU SU782690859A patent/SU795434A3/ru active
- 1978-11-29 BG BG041559A patent/BG28684A3/xx unknown
- 1978-11-29 CS CS787857A patent/CS199750B2/cs unknown
- 1978-11-29 PL PL21132778A patent/PL211327A1/pl unknown
- 1978-11-29 FR FR7833709A patent/FR2410435A1/fr not_active Withdrawn
- 1978-11-29 BE BE192028A patent/BE872384A/xx unknown
- 1978-11-29 AU AU42056/78A patent/AU4205678A/en active Pending
- 1978-11-30 US US05/965,215 patent/US4221801A/en not_active Expired - Lifetime
- 1978-11-30 DD DD78209435A patent/DD141404A5/de unknown

Also Published As

Publication number	Publication date
NL7713267A (nl)	1979-06-06
IT1100380B (it)	1985-09-28
BE872384A (fr)	1979-05-29
TR19992A (tr)	1980-05-15
FR2410435A1 (fr)	1979-06-29
IL56066A0 (en)	1979-01-31
US4221801A (en)	1980-09-09
ZA786277B (en)	1980-06-25
IT7830292A0 (it)	1978-11-28
GB2008951A (en)	1979-06-13
DE2851376A1 (de)	1979-06-07
DD141404A5 (de)	1980-04-30
JPS5513257A (en)	1980-01-30
SU795434A3 (ru)	1981-01-07
PL211327A1 (pl)	1979-07-30
NZ189028A (en)	1980-08-26
DK531378A (da)	1979-06-02
BG28684A3 (en)	1980-06-16
AU4205678A (en)	1979-06-07

Publication	Publication Date	Title
EP0021506B1 (en)	1983-09-07	New pyrazoline derivatives, method of preparing the new compounds, as well as insecticidal composition on the basis of these new compounds
DK155597B (da)	1989-04-24	Urinstofderivater samt insekticidt middel indeholdende disse derivater
US4399152A (en)	1983-08-16	Substituted benzoyl ureas as insecticides
DE3779814T2 (de)	1993-02-04	Insektentoetende n-substituierte-n'-substituierte-n,n'-diacylhydrazine.
JPH0414660B2 (pl)	1992-03-13
JPS62209053A (ja)	1987-09-14	殺虫性ｎ′−置換−ｎ−アルキルカルボニル−ｎ′−アシルヒドラジン
DE68908789T2 (de)	1994-04-14	Insectizide N'-substituierte-N-alkylcarbonyl-N'-acylhydrazine und N'-substituierte-N-acyl-N'-alkylcarbonyl hydrazine.
KR910008136B1 (ko)	1991-10-10	벤조일우레아 화합물의 제조방법
DE2304584A1 (de)	1973-08-16	Neue pyrazolinverbindungen mit insektizidwirksamkeit
JP2593302B2 (ja)	1997-03-26	新規１−ジメチルカルバモイル−３−置換−５−置換−１ｈ−１，２，４−トリアゾール、この新規化合物を含有する組成物およびその利用方法
KR950002155B1 (ko)	1995-03-14	살충성 6-아릴-피리딘 티오세미카르바존 및 그의 조성물
CZ20022900A3 (cs)	2003-01-15	Pesticidové preparáty a jejich pouľití jako ochranných látek
CS242895B2 (en)	1986-05-15	Insecticide against mites,moths and method of efficient substances production
CA1173048A (en)	1984-08-21	Pyrazoline derivatives, method of preparing the new compounds, as well as insecticidal compositions on the basis of these compounds
JP2916736B2 (ja)	1999-07-05	種子消毒剤
JPS59176243A (ja)	1984-10-05	新規ベンゾイル尿素化合物およびその製造方法並びにこの化合物を含有する殺虫−殺ダニ剤
CS199750B2 (en)	1980-07-31	Agent for treatment of soil or seeds for sowing against phythopathogic microorganisms
GB2038305A (en)	1980-07-23	Plant growth regulating compositions
EP0031974A2 (en)	1981-07-15	New urea compounds and thiourea compounds, method of preparing the new compounds, and insecticidal compositions on the basis of these compounds
PL100182B1 (pl)	1978-09-30	Srodek grzybobojczy
JPS62234055A (ja)	1987-10-14	殺虫活性を有するｎ′−置換−ｎ−アシル−ｎ′−アルキルカルボニルヒドラジン
JPS5919085B2 (ja)	1984-05-02	サツソウザイ
JPH03284602A (ja)	1991-12-16	農園芸用殺菌剤
JPS59164708A (ja)	1984-09-17	除草剤組成物
JPH01190607A (ja)	1989-07-31	水田用除草剤組成物