CS207659B2 - Means for annihilating the non-desirous vegetation and method of making the active component - Google Patents

Means for annihilating the non-desirous vegetation and method of making the active component Download PDF

Info

Publication number: CS207659B2
Authority: CS; Czechoslovakia
Prior art keywords: formula; active ingredient; composition according; acetate; alkyl
Prior art date: 1977-08-26

Application number

CS785551A

Other languages

Czech (cs)

English (en)

Inventor

Richard F Sauers

Original Assignee

Du Pont

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.)

1977-08-26

Filing date

1978-08-25

Publication date

1981-08-31

1978-08-25 Application filed by Du Pont filed Critical Du Pont

1981-08-31 Publication of CS207659B2 publication Critical patent/CS207659B2/cs

Links

238000004519 manufacturing process Methods 0.000 title description 3
150000001875 compounds Chemical class 0.000 claims abstract description 63
239000000460 chlorine Substances 0.000 claims abstract description 24
125000000217 alkyl group Chemical group 0.000 claims abstract description 21
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 21
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 21
239000001257 hydrogen Substances 0.000 claims abstract description 19
229910052801 chlorine Inorganic materials 0.000 claims abstract description 17
238000000034 method Methods 0.000 claims abstract description 16
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 11
239000003085 diluting agent Substances 0.000 claims abstract description 10
239000007788 liquid Substances 0.000 claims abstract description 7
239000004094 surface-active agent Substances 0.000 claims abstract description 7
239000007787 solid Substances 0.000 claims abstract description 6
238000002360 preparation method Methods 0.000 claims abstract description 5
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 4
229910052717 sulfur Chemical group 0.000 claims abstract description 4
239000011593 sulfur Chemical group 0.000 claims abstract description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 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
239000000203 mixture Substances 0.000 claims description 44
239000004480 active ingredient Substances 0.000 claims description 26
-1 3-bromopropoxy, amino Chemical group 0.000 claims description 25
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 21
125000001309 chloro group Chemical group Cl* 0.000 claims description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 7
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 7
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 6
239000011575 calcium Substances 0.000 claims description 6
229910052791 calcium Inorganic materials 0.000 claims description 6
239000011737 fluorine Substances 0.000 claims description 6
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125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
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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 description 4
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241000608847 Gnaphalium Species 0.000 description 1
201000005569 Gout Diseases 0.000 description 1
235000021506 Ipomoea Nutrition 0.000 description 1
241000207783 Ipomoea Species 0.000 description 1
240000007472 Leucaena leucocephala Species 0.000 description 1
235000010643 Leucaena leucocephala Nutrition 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241001268782 Paspalum dilatatum Species 0.000 description 1
240000004370 Pastinaca sativa Species 0.000 description 1
235000017769 Pastinaca sativa subsp sativa Nutrition 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
240000002181 Portulaca pilosa Species 0.000 description 1
101100191082 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GLC7 gene Proteins 0.000 description 1
244000007853 Sarothamnus scoparius Species 0.000 description 1
101100274406 Schizosaccharomyces pombe (strain 972 / ATCC 24843) cid1 gene Proteins 0.000 description 1
BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
244000275012 Sesbania cannabina Species 0.000 description 1
241000533293 Sesbania emerus Species 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
235000010749 Vicia faba Nutrition 0.000 description 1
240000006677 Vicia faba Species 0.000 description 1
235000002098 Vicia faba var. major Nutrition 0.000 description 1
241001148683 Zostera marina Species 0.000 description 1
239000013543 active substance Substances 0.000 description 1
230000001154 acute effect Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
150000004703 alkoxides Chemical class 0.000 description 1
150000005840 aryl radicals Chemical group 0.000 description 1
238000003556 assay Methods 0.000 description 1
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 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
ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 description 1
CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910000281 calcium bentonite Inorganic materials 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000000969 carrier Substances 0.000 description 1
238000012993 chemical processing Methods 0.000 description 1
WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
TXHWYSOQHNMOOU-UHFFFAOYSA-N chloro(diethoxy)phosphane Chemical compound CCOP(Cl)OCC TXHWYSOQHNMOOU-UHFFFAOYSA-N 0.000 description 1
229910052804 chromium Inorganic materials 0.000 description 1
239000011651 chromium Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
235000012343 cottonseed oil Nutrition 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
230000035613 defoliation Effects 0.000 description 1
239000003599 detergent Substances 0.000 description 1
RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
ZLBHBEALMAIEGY-UHFFFAOYSA-N ethyl 2-(oxo-lambda5-phosphanylidyne)acetate Chemical compound C(C)OC(C#P=O)=O ZLBHBEALMAIEGY-UHFFFAOYSA-N 0.000 description 1
125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
238000005187 foaming Methods 0.000 description 1
208000006278 hypochromic anemia Diseases 0.000 description 1
230000006872 improvement Effects 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
230000000977 initiatory effect Effects 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
238000007689 inspection Methods 0.000 description 1
239000011630 iodine Chemical group 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
239000002609 medium Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 1
244000045947 parasite Species 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
235000020030 perry Nutrition 0.000 description 1
230000002688 persistence Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000006187 pill Substances 0.000 description 1
229940051841 polyoxyethylene ether Drugs 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
230000005855 radiation Effects 0.000 description 1
238000012552 review Methods 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
229910052711 selenium Inorganic materials 0.000 description 1
239000011669 selenium Substances 0.000 description 1
229910000104 sodium hydride Inorganic materials 0.000 description 1
239000012312 sodium hydride Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000000243 solution Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000003826 tablet Substances 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1
JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6527—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
- C07F9/6533—Six-membered rings
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/141—Esters of phosphorous acids
- C07F9/145—Esters of phosphorous acids with hydroxyaryl compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
- C07F9/32—Esters thereof
- C07F9/3205—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/3211—Esters of acyclic saturated acids which can have further substituents on alkyl
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
- C07F9/36—Amides thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/53—Organo-phosphine oxides; Organo-phosphine thioxides
- C07F9/5304—Acyclic saturated phosphine oxides or thioxides
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/572—Five-membered rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/58—Pyridine rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/650952—Six-membered rings having the nitrogen atoms in the positions 1 and 4

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Biochemistry (AREA)
Molecular Biology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CS785551A 1977-08-26 1978-08-25 Means for annihilating the non-desirous vegetation and method of making the active component CS207659B2 (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date
US82821377A	1977-08-26	1977-08-26
US91475778A	1978-06-14	1978-06-14
US91738878A	1978-06-23	1978-06-23

Publications (1)

Publication Number	Publication Date
CS207659B2 true CS207659B2 (en)	1981-08-31

Family

ID=27420203

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS785551A CS207659B2 (en)	1977-08-26	1978-08-25	Means for annihilating the non-desirous vegetation and method of making the active component

Country Status (15)

Country	Link
EP (1)	EP0001331A1 (pt)
JP (1)	JPS5444617A (pt)
BR (1)	BR7805517A (pt)
CS (1)	CS207659B2 (pt)
DK (1)	DK324878A (pt)
ES (1)	ES472861A1 (pt)
FI (1)	FI782605A7 (pt)
GB (1)	GB2004889A (pt)
GR (1)	GR65277B (pt)
IL (1)	IL55436A0 (pt)
IT (1)	IT1098195B (pt)
NO (1)	NO782905L (pt)
NZ (1)	NZ188261A (pt)
PL (1)	PL113571B1 (pt)
PT (1)	PT68480A (pt)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3238958A1 (de) *	1982-09-10	1984-03-15	Hoechst Ag, 6230 Frankfurt	Phosphorhaltige funktionelle essigsaeurederivate, verfahren zu ihrer herstellung und sie enthaltende heribizide und wachstumsregulierende mittel
DE3313070A1 (de) *	1983-04-12	1984-10-18	Bayer Ag, 5090 Leverkusen	Chlorierte phosphorylmethylcarbonyl-derivate, verfahren zu ihrer herstellung und ihre verwendung in pflanzenschutmitteln
JPS61204735A (ja) *	1985-02-06	1986-09-10	Nec Corp	デ−タ駆動浮動小数点演算回路
CN103071209A (zh)	2005-11-17	2013-05-01	周吉尼克斯股份有限公司	用无针注射递送粘稠制剂
WO2011124553A2 (de) *	2010-04-09	2011-10-13	Bayer Cropscience Ag	Verwendung von derivaten der (1-cyancyclopropyl)phenylphosphinsäure, deren ester und/oder deren salze zur steigerung der toleranz in pflanzen gegenüber abiotischem stress
PL226167B1 (pl)	2010-09-17	2017-06-30	Deep Ocean Tech Spółka Z Ograniczoną Odpowiedzialnością	Pomieszczenie podwodno-nadwodne, zwlaszcza do celow mieszkalnych

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1071755A (fr) *	1951-09-25	1954-09-06	Ciba Geigy	Nouveaux composés organiques halogénés et phosphorés, et procédé pour leur préparation

1978
- 1978-07-20 DK DK324878A patent/DK324878A/da not_active Application Discontinuation
- 1978-08-24 JP JP10238678A patent/JPS5444617A/ja active Pending
- 1978-08-24 IT IT26998/78A patent/IT1098195B/it active
- 1978-08-25 GB GB7834653A patent/GB2004889A/en not_active Withdrawn
- 1978-08-25 FI FI782605A patent/FI782605A7/fi unknown
- 1978-08-25 PL PL1978209224A patent/PL113571B1/pl unknown
- 1978-08-25 EP EP78300325A patent/EP0001331A1/en not_active Withdrawn
- 1978-08-25 GR GR57076A patent/GR65277B/el unknown
- 1978-08-25 NZ NZ188261A patent/NZ188261A/xx unknown
- 1978-08-25 IL IL7855436A patent/IL55436A0/xx unknown
- 1978-08-25 NO NO782905A patent/NO782905L/no unknown
- 1978-08-25 CS CS785551A patent/CS207659B2/cs unknown
- 1978-08-25 PT PT68480A patent/PT68480A/pt unknown
- 1978-08-25 BR BR7805517A patent/BR7805517A/pt unknown
- 1978-08-25 ES ES472861A patent/ES472861A1/es not_active Expired

Also Published As

Publication number	Publication date
FI782605A7 (fi)	1979-02-27
BR7805517A (pt)	1979-04-17
ES472861A1 (es)	1979-10-16
GB2004889A (en)	1979-04-11
JPS5444617A (en)	1979-04-09
IL55436A0 (en)	1978-10-31
PT68480A (en)	1978-09-01
NO782905L (no)	1979-02-27
PL113571B1 (en)	1980-12-31
PL209224A1 (pl)	1979-06-04
GR65277B (en)	1980-07-31
IT7826998A0 (it)	1978-08-24
EP0001331A1 (en)	1979-04-04
DK324878A (da)	1979-02-27
NZ188261A (en)	1980-12-19
IT1098195B (it)	1985-09-07

Publication	Publication Date	Title
RU2042667C1 (ru)	1995-08-27	Производные 4-бензоилпиразола
EP0184385B1 (en)	1990-09-26	N-[(4,6-Dimethoxypyrimidin-2-YL)Aminocarbonyl]-3-trifluoromethylpyridine-2-sulfonamide or salts thereof, herbicidal composition containing the same, and processs for the production of the compound
SU1215623A3 (ru)	1986-02-28	Способ получени пиразолилфосфатов
JP2615228B2 (ja)	1997-05-28	フルオロエトキシアミノトリアジン
US4191554A (en)	1980-03-04	Herbicidal benzamides
CS207659B2 (en)	1981-08-31	Means for annihilating the non-desirous vegetation and method of making the active component
CN110066286B (zh)	2020-06-16	具生物活性苯基吡唑啉类化合物及其制备方法与应用
US4023956A (en)	1977-05-17	Amide phosphorothiolate herbicides
CS199286B2 (en)	1980-07-31	Fungicides,insecticides,acaricides,nematocides and herbicides and method of producing active compounds
JPS6348248A (ja)	1988-02-29	ベンゾヒドロキサム酸誘導体
JPS6325588B2 (pt)	1988-05-26
US4319917A (en)	1982-03-16	N-(2-Cyanoalkoxy)methyl-N-(2-,3-, or 6-alkylphenyl)-α-haloacetamides
EP0001018A1 (en)	1979-03-07	Herbicidal phosphonates and preparation and use thereof
US4217312A (en)	1980-08-12	1-Alkyl-2,2-dichloro-2(phosphinyl)acetates
US4326058A (en)	1982-04-20	Organo-phosphoric esters and their production and use
US4225521A (en)	1980-09-30	Herbicidal phosphonates
US4309358A (en)	1982-01-05	Agricultural stannanamines
US4015974A (en)	1977-04-05	Amido phosphorothiolates
JP2997287B2 (ja)	2000-01-11	３―置換アルキルサリチレートを基礎としたフエノキシスルホニル尿素、それらの製造方法およびそれらの除草剤および植物生長調整剤としての使用方法
EP0015078B1 (en)	1984-07-04	Organo-phosphoric esters, their production and use as pesticides, as well as the intermediates thereof and their production
JP2618639B2 (ja)	1997-06-11	シクロヘキセノン誘導体およびそれを有効成分とする除草剤
US3647850A (en)	1972-03-07	Fluorine substituted benzyl dithiocarbamates and their production and use
KR900005517B1 (ko)	1990-07-30	신규 제초제 피리디늄 내부염 및 일이드와 그들의 제조방법
EP0255800B1 (en)	1991-07-17	Benzohydroxamic acid derivatives
EP0190945A2 (en)	1986-08-13	Herbicidal propylene oxide derivatives