NO831952L - Nye urea-derivater og herbicide preparater - Google Patents

Nye urea-derivater og herbicide preparater

Info

Publication number: NO831952L
Authority: NO; Norway
Prior art keywords: butylisoxazol; methyl; urea; ylmethyl; herbicides
Prior art date: 1982-06-01

Application number

NO831952A

Other languages

English (en)

Norwegian (no)

Inventor

John Krenzer

Original Assignee

Velsicol Chemical Corp

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.)

1982-06-01

Filing date

1983-05-31

Publication date

1983-12-02

1983-05-31 Application filed by Velsicol Chemical Corp filed Critical Velsicol Chemical Corp

1983-12-02 Publication of NO831952L publication Critical patent/NO831952L/no

Links

239000004009 herbicide Substances 0.000 title claims description 39
230000002363 herbicidal effect Effects 0.000 title description 13
238000002360 preparation method Methods 0.000 title description 9
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical class NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 title 1
150000001875 compounds Chemical class 0.000 claims description 40
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238000000034 method Methods 0.000 claims description 6
231100000331 toxic Toxicity 0.000 claims description 4
230000002588 toxic effect Effects 0.000 claims description 4
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125000000217 alkyl group Chemical group 0.000 claims description 2
-1 5-t-butylisoxazol-3-yl Chemical group 0.000 description 28
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
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FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 1
CCGPUGMWYLICGL-UHFFFAOYSA-N Neburon Chemical compound CCCCN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 CCGPUGMWYLICGL-UHFFFAOYSA-N 0.000 description 1
UMKANAFDOQQUKE-UHFFFAOYSA-N Nitralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(C)(=O)=O)C=C1[N+]([O-])=O UMKANAFDOQQUKE-UHFFFAOYSA-N 0.000 description 1
YGLMVCVJLXREAK-UHFFFAOYSA-N Noruron Chemical compound C12CCCC2C2CC(NC(=O)N(C)C)C1C2 YGLMVCVJLXREAK-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
235000015225 Panicum colonum Nutrition 0.000 description 1
244000236458 Panicum colonum Species 0.000 description 1
SGEJQUSYQTVSIU-UHFFFAOYSA-N Pebulate Chemical compound CCCCN(CC)C(=O)SCCC SGEJQUSYQTVSIU-UHFFFAOYSA-N 0.000 description 1
235000017337 Persicaria hydropiper Nutrition 0.000 description 1
240000000275 Persicaria hydropiper Species 0.000 description 1
240000005218 Phyla nodiflora Species 0.000 description 1
239000005595 Picloram Substances 0.000 description 1
244000292697 Polygonum aviculare Species 0.000 description 1
235000006386 Polygonum aviculare Nutrition 0.000 description 1
235000004442 Polygonum persicaria Nutrition 0.000 description 1
244000234609 Portulaca oleracea Species 0.000 description 1
235000001855 Portulaca oleracea Nutrition 0.000 description 1
235000002357 Ribes grossularia Nutrition 0.000 description 1
244000171263 Ribes grossularia Species 0.000 description 1
235000005291 Rumex acetosa Nutrition 0.000 description 1
235000015422 Rumex crispus ssp. crispus Nutrition 0.000 description 1
235000015426 Rumex crispus ssp. fauriei Nutrition 0.000 description 1
244000207667 Rumex vesicarius Species 0.000 description 1
241000202758 Scirpus Species 0.000 description 1
244000275012 Sesbania cannabina Species 0.000 description 1
241000511959 Silene latifolia subsp. alba Species 0.000 description 1
240000002439 Sorghum halepense Species 0.000 description 1
241000960310 Spergula Species 0.000 description 1
240000001949 Taraxacum officinale Species 0.000 description 1
235000005187 Taraxacum officinale ssp. officinale Nutrition 0.000 description 1
NBQCNZYJJMBDKY-UHFFFAOYSA-N Terbacil Chemical compound CC=1NC(=O)N(C(C)(C)C)C(=O)C=1Cl NBQCNZYJJMBDKY-UHFFFAOYSA-N 0.000 description 1
240000008488 Thlaspi arvense Species 0.000 description 1
235000008214 Thlaspi arvense Nutrition 0.000 description 1
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
HFBWPRKWDIRYNX-UHFFFAOYSA-N Trietazine Chemical compound CCNC1=NC(Cl)=NC(N(CC)CC)=N1 HFBWPRKWDIRYNX-UHFFFAOYSA-N 0.000 description 1
235000005324 Typha latifolia Nutrition 0.000 description 1
240000006064 Urena lobata Species 0.000 description 1
241000201404 Verbascum blattaria Species 0.000 description 1
235000010599 Verbascum thapsus Nutrition 0.000 description 1
244000178289 Verbascum thapsus Species 0.000 description 1
244000145469 Vernonia anthelmintica Species 0.000 description 1
235000013018 Vernonia anthelmintica Nutrition 0.000 description 1
241000219873 Vicia Species 0.000 description 1
208000000260 Warts Diseases 0.000 description 1
208000027418 Wounds and injury Diseases 0.000 description 1
241001148683 Zostera marina Species 0.000 description 1
239000012190 activator Substances 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
235000012735 amaranth Nutrition 0.000 description 1
239000004178 amaranth Substances 0.000 description 1
RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 1
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208000014347 autosomal dominant hyaline body myopathy Diseases 0.000 description 1
MCOQHIWZJUDQIC-UHFFFAOYSA-N barban Chemical compound ClCC#CCOC(=O)NC1=CC=CC(Cl)=C1 MCOQHIWZJUDQIC-UHFFFAOYSA-N 0.000 description 1
SMDHCQAYESWHAE-UHFFFAOYSA-N benfluralin Chemical compound CCCCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O SMDHCQAYESWHAE-UHFFFAOYSA-N 0.000 description 1
150000001558 benzoic acid derivatives Chemical class 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
235000005770 birds nest Nutrition 0.000 description 1
OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 1
229910021538 borax Inorganic materials 0.000 description 1
CURLHBZYTFVCRG-UHFFFAOYSA-N butan-2-yl n-(3-chlorophenyl)carbamate Chemical compound CCC(C)OC(=O)NC1=CC=CC(Cl)=C1 CURLHBZYTFVCRG-UHFFFAOYSA-N 0.000 description 1
229950004243 cacodylic acid Drugs 0.000 description 1
DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000000969 carrier Substances 0.000 description 1
BIWJNBZANLAXMG-UHFFFAOYSA-N chlordane Chemical compound ClC1=C(Cl)C2(Cl)C3CC(Cl)C(Cl)C3C1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-UHFFFAOYSA-N 0.000 description 1
VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
IVUXTESCPZUGJC-UHFFFAOYSA-N chloroxuron Chemical compound C1=CC(NC(=O)N(C)C)=CC=C1OC1=CC=C(Cl)C=C1 IVUXTESCPZUGJC-UHFFFAOYSA-N 0.000 description 1
CWJSHJJYOPWUGX-UHFFFAOYSA-N chlorpropham Chemical compound CC(C)OC(=O)NC1=CC=CC(Cl)=C1 CWJSHJJYOPWUGX-UHFFFAOYSA-N 0.000 description 1
244000118869 coast club rush Species 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 description 1
PPJXIHLNYDVTDI-UHFFFAOYSA-N dicloralurea Chemical compound ClC(Cl)(Cl)C(O)NC(=O)NC(O)C(Cl)(Cl)Cl PPJXIHLNYDVTDI-UHFFFAOYSA-N 0.000 description 1
SYJFEGQWDCRVNX-UHFFFAOYSA-N diquat Chemical compound C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 SYJFEGQWDCRVNX-UHFFFAOYSA-N 0.000 description 1
SDIXRDNYIMOKSG-UHFFFAOYSA-L disodium methyl arsenate Chemical compound [Na+].[Na+].C[As]([O-])([O-])=O SDIXRDNYIMOKSG-UHFFFAOYSA-L 0.000 description 1
UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000012990 dithiocarbamate Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
XXOYNJXVWVNOOJ-UHFFFAOYSA-N fenuron Chemical compound CN(C)C(=O)NC1=CC=CC=C1 XXOYNJXVWVNOOJ-UHFFFAOYSA-N 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
235000013305 food Nutrition 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
239000003966 growth inhibitor Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
208000014674 injury Diseases 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
239000002075 main ingredient Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
PSGAAPLEWMOORI-PEINSRQWSA-N medroxyprogesterone acetate Chemical compound C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2CC[C@]2(C)[C@@](OC(C)=O)(C(C)=O)CC[C@H]21 PSGAAPLEWMOORI-PEINSRQWSA-N 0.000 description 1
MYURAHUSYDVWQA-UHFFFAOYSA-N methyl n'-(4-chlorophenyl)-n,n-dimethylcarbamimidate Chemical compound COC(N(C)C)=NC1=CC=C(Cl)C=C1 MYURAHUSYDVWQA-UHFFFAOYSA-N 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
235000019713 millet Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000009526 moderate injury Effects 0.000 description 1
DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 description 1
JITOKQVGRJSHHA-UHFFFAOYSA-M monosodium methyl arsenate Chemical compound [Na+].C[As](O)([O-])=O JITOKQVGRJSHHA-UHFFFAOYSA-M 0.000 description 1
BMLIZLVNXIYGCK-UHFFFAOYSA-N monuron Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C=C1 BMLIZLVNXIYGCK-UHFFFAOYSA-N 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 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
239000000575 pesticide Substances 0.000 description 1
JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
239000003279 phenylacetic acid Substances 0.000 description 1
229960003424 phenylacetic acid Drugs 0.000 description 1
XEBWQGVWTUSTLN-UHFFFAOYSA-M phenylmercury acetate Chemical compound CC(=O)O[Hg]C1=CC=CC=C1 XEBWQGVWTUSTLN-UHFFFAOYSA-M 0.000 description 1
NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 description 1
239000002373 plant growth inhibitor Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
TZLVRPLSVNESQC-UHFFFAOYSA-N potassium azide Chemical compound [K+].[N-]=[N+]=[N-] TZLVRPLSVNESQC-UHFFFAOYSA-N 0.000 description 1
GKKCIDNWFBPDBW-UHFFFAOYSA-M potassium cyanate Chemical compound [K]OC#N GKKCIDNWFBPDBW-UHFFFAOYSA-M 0.000 description 1
ISEUFVQQFVOBCY-UHFFFAOYSA-N prometon Chemical compound COC1=NC(NC(C)C)=NC(NC(C)C)=N1 ISEUFVQQFVOBCY-UHFFFAOYSA-N 0.000 description 1
MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 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
229910052903 pyrophyllite Inorganic materials 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000012047 saturated solution Substances 0.000 description 1
235000003513 sheep sorrel Nutrition 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
HKAMKLBXTLTVCN-UHFFFAOYSA-N simeton Chemical compound CCNC1=NC(NCC)=NC(OC)=N1 HKAMKLBXTLTVCN-UHFFFAOYSA-N 0.000 description 1
201000010153 skin papilloma Diseases 0.000 description 1
235000010339 sodium tetraborate Nutrition 0.000 description 1
239000004328 sodium tetraborate Substances 0.000 description 1
NTOCDDPMRUNYHP-UHFFFAOYSA-M sodium;2-(2,4,5-trichlorophenoxy)ethyl sulfate Chemical compound [Na+].[O-]S(=O)(=O)OCCOC1=CC(Cl)=C(Cl)C=C1Cl NTOCDDPMRUNYHP-UHFFFAOYSA-M 0.000 description 1
238000009331 sowing Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
235000005765 wild carrot Nutrition 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
- 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Plural Heterocyclic Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

NO831952A 1982-06-01 1983-05-31 Nye urea-derivater og herbicide preparater NO831952L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US38339182A	1982-06-01	1982-06-01

Publications (1)

Publication Number	Publication Date
NO831952L true NO831952L (no)	1983-12-02

Family

ID=23512920

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO831952A NO831952L (no)	1982-06-01	1983-05-31	Nye urea-derivater og herbicide preparater

Country Status (24)

Country	Link
JP (1)	JPS58219185A (ro)
KR (1)	KR860000849B1 (ro)
AU (1)	AU555665B2 (ro)
BE (1)	BE896883A (ro)
BR (1)	BR8302575A (ro)
CA (1)	CA1189512A (ro)
CH (1)	CH654006A5 (ro)
DD (1)	DD211943A5 (ro)
DE (1)	DE3319557A1 (ro)
DK (1)	DK246383A (ro)
ES (1)	ES8407044A1 (ro)
FR (1)	FR2527607A1 (ro)
GB (1)	GB2121034B (ro)
GR (1)	GR78262B (ro)
IT (1)	IT1172261B (ro)
NL (1)	NL8301659A (ro)
NO (1)	NO831952L (ro)
NZ (1)	NZ203871A (ro)
PH (1)	PH19467A (ro)
RO (1)	RO87127A (ro)
SE (1)	SE8302972L (ro)
SU (1)	SU1209019A3 (ro)
YU (1)	YU117583A (ro)
ZA (1)	ZA832937B (ro)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4507145A (en) *	1980-02-19	1985-03-26	Ppg Industries, Inc.	Herbicidal 3-[substituted 3- or 5-isoxazolyl]-1-4-, or 5-substituted-2-imidazolidinones

1983
- 1983-04-08 CA CA000425522A patent/CA1189512A/en not_active Expired
- 1983-04-13 NZ NZ203871A patent/NZ203871A/en unknown
- 1983-04-22 GB GB08310916A patent/GB2121034B/en not_active Expired
- 1983-04-26 KR KR1019830001763A patent/KR860000849B1/ko not_active Expired
- 1983-04-26 ZA ZA832937A patent/ZA832937B/xx unknown
- 1983-04-27 CH CH2261/83A patent/CH654006A5/de not_active IP Right Cessation
- 1983-05-02 PH PH28842A patent/PH19467A/en unknown
- 1983-05-10 NL NL8301659A patent/NL8301659A/nl not_active Application Discontinuation
- 1983-05-17 BR BR8302575A patent/BR8302575A/pt unknown
- 1983-05-23 SU SU833595055A patent/SU1209019A3/ru active
- 1983-05-24 IT IT48358/83A patent/IT1172261B/it active
- 1983-05-26 SE SE8302972A patent/SE8302972L/xx not_active Application Discontinuation
- 1983-05-26 ES ES522736A patent/ES8407044A1/es not_active Expired
- 1983-05-26 YU YU01175/83A patent/YU117583A/xx unknown
- 1983-05-30 FR FR8308927A patent/FR2527607A1/fr not_active Withdrawn
- 1983-05-30 BE BE0/210876A patent/BE896883A/fr not_active IP Right Cessation
- 1983-05-30 GR GR71505A patent/GR78262B/el unknown
- 1983-05-30 DE DE19833319557 patent/DE3319557A1/de not_active Withdrawn
- 1983-05-31 DK DK246383A patent/DK246383A/da not_active Application Discontinuation
- 1983-05-31 AU AU15217/83A patent/AU555665B2/en not_active Expired - Fee Related
- 1983-05-31 NO NO831952A patent/NO831952L/no unknown
- 1983-05-31 DD DD83251540A patent/DD211943A5/de unknown
- 1983-05-31 RO RO83111130A patent/RO87127A/ro unknown
- 1983-06-01 JP JP58097779A patent/JPS58219185A/ja active Pending

Also Published As

Publication number	Publication date
SE8302972L (sv)	1983-12-02
RO87127B (ro)	1985-12-01
DK246383A (da)	1983-12-02
GB2121034B (en)	1986-02-05
DD211943A5 (de)	1984-08-01
CA1189512A (en)	1985-06-25
JPS58219185A (ja)	1983-12-20
YU117583A (en)	1986-12-31
DK246383D0 (da)	1983-05-31
IT1172261B (it)	1987-06-18
KR860000849B1 (ko)	1986-07-09
SU1209019A3 (ru)	1986-01-30
BR8302575A (pt)	1984-01-17
ZA832937B (en)	1984-01-25
GB2121034A (en)	1983-12-14
ES522736A0 (es)	1984-09-01
ES8407044A1 (es)	1984-09-01
RO87127A (ro)	1985-12-20
FR2527607A1 (fr)	1983-12-02
AU1521783A (en)	1984-01-19
SE8302972D0 (sv)	1983-05-26
DE3319557A1 (de)	1983-12-01
GR78262B (ro)	1984-09-26
BE896883A (fr)	1983-09-16
NL8301659A (nl)	1984-01-02
GB8310916D0 (en)	1983-05-25
NZ203871A (en)	1985-05-31
CH654006A5 (de)	1986-01-31
IT8348358A0 (it)	1983-05-24
KR840005136A (ko)	1984-11-03
AU555665B2 (en)	1986-10-02
PH19467A (en)	1986-05-14

Publication	Publication Date	Title
US4116670A (en)	1978-09-26	Dioxane substituted amides
US4110101A (en)	1978-08-29	Dioxepane substituted amides
US4289524A (en)	1981-09-15	Herbicidal 3-(tetrahydrobenzothiazol-2-yl)tetrahydro-1,3,5-oxadiazin-4-ones
US3870732A (en)	1975-03-11	Mixed salts of aluminum
US3864377A (en)	1975-02-04	Aryl urea carbonates
US4022610A (en)	1977-05-10	Herbicidal mixed salts of magnesium
US3910974A (en)	1975-10-07	Mixed salts of magnesium of 2-methoxy-3,6-dichlorobenzoic acid and a carboxylic acid
NO831774L (no)	1983-11-21	Nye herbiside forbindelser.
NO832269L (no)	1983-12-27	Furfurylamider av fenoksy-fenoksy-alkansyrer.
NO831952L (no)	1983-12-02	Nye urea-derivater og herbicide preparater
CA1188693A (en)	1985-06-11	Triazine herbicides and plant growth regulants
US3860644A (en)	1975-01-14	Composition of matter
US3900485A (en)	1975-08-19	New substituted 1,2,4-thiadiazolidine-3,5-diones
US4197114A (en)	1980-04-08	Alkyl N-3-alkoxy-, and N-3,5-dialkoxybenzoyl-N-isopropylaminoacetate herbicides
US3827875A (en)	1974-08-06	Dialkyl acetals of heterocyclic ureidoacetaldehyde
US4354032A (en)	1982-10-12	Alkyl N-3-halo-,N-3,5-dihalobenzoyl-N-isopropylaminoacetate herbicides
US3941580A (en)	1976-03-02	Herbicidal compositions
KR860000133B1 (ko)	1986-02-26	페녹시 벤조산의 헤테로 사이클릭 에스테르의 제조방법
US4052193A (en)	1977-10-04	1-(5-t-butyl-1,3,4-thiadiazol-2-yl)-3-methyl-5-octanoyloxy-1,3-imidazolidin-2-one herbicide
US4491469A (en)	1985-01-01	Herbicidal oxime esters of 2-methoxy-3,6-dichlorobenzoic acid
KR860000846B1 (ko)	1986-07-09	페녹시페녹시 알칸산의 헤테로사이클릭 아미드의 제조방법
US4402728A (en)	1983-09-06	Heterocyclic anilines
US4397677A (en)	1983-08-09	Dioxolane substituted 2,6-dinitroanilines
NO141991B (no)	1980-03-03	1,2,4-triazolidin-3-on-derivater med herbicid virkning
US3984228A (en)	1976-10-05	Thiadiazole substituted imidazolidines