IL23253A - Soil treatment compositions containing a 2-chloro-benzoxazole - Google Patents

Soil treatment compositions containing a 2-chloro-benzoxazole

Info

Publication number: IL23253A
Authority: IL; Israel
Prior art keywords: chloro; soil; benzoxazole; admixture; treatment compositions
Prior art date: 1964-04-29

Application number

IL23253A

Other languages

English (en)

Original Assignee

Bayer Ag

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.)

1964-04-29

Filing date

1965-03-30

Publication date

1968-08-22

1965-03-30 Application filed by Bayer Ag filed Critical Bayer Ag

1968-08-22 Publication of IL23253A publication Critical patent/IL23253A/en

Links

239000002689 soil Substances 0.000 title claims description 23
BBVQDWDBTWSGHQ-UHFFFAOYSA-N 2-chloro-1,3-benzoxazole Chemical compound C1=CC=C2OC(Cl)=NC2=C1 BBVQDWDBTWSGHQ-UHFFFAOYSA-N 0.000 title claims description 13
239000000203 mixture Substances 0.000 title claims description 11
239000002904 solvent Substances 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 5
239000003995 emulsifying agent Substances 0.000 claims description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
239000003085 diluting agent Substances 0.000 claims description 4
239000007787 solid Substances 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
239000004480 active ingredient Substances 0.000 claims description 3
239000000839 emulsion Substances 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
239000003960 organic solvent Substances 0.000 claims description 3
230000000249 desinfective effect Effects 0.000 claims description 2
125000001188 haloalkyl group Chemical group 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
238000000034 method Methods 0.000 claims description 2
239000007788 liquid Substances 0.000 claims 2
239000004606 Fillers/Extenders Substances 0.000 claims 1
125000000217 alkyl group Chemical group 0.000 claims 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
150000001875 compounds Chemical class 0.000 description 14
241000244206 Nematoda Species 0.000 description 13
-1 2 , 5-dichloro-7-methyl-benzoxazole Chemical compound 0.000 description 4
206010061217 Infestation Diseases 0.000 description 4
238000009472 formulation Methods 0.000 description 4
230000001069 nematicidal effect Effects 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
150000000183 1,3-benzoxazoles Chemical class 0.000 description 3
241000196324 Embryophyta Species 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
238000009835 boiling Methods 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 3
239000000243 solution Substances 0.000 description 3
PWYDOMHIKFHJIW-UHFFFAOYSA-N 2,5,7-trichloro-1,3-benzoxazole Chemical compound ClC1=CC(Cl)=C2OC(Cl)=NC2=C1 PWYDOMHIKFHJIW-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
BSQLQMLFTHJVKS-UHFFFAOYSA-N 2-chloro-1,3-benzothiazole Chemical compound C1=CC=C2SC(Cl)=NC2=C1 BSQLQMLFTHJVKS-UHFFFAOYSA-N 0.000 description 2
241000680417 Aphelenchoides ritzemabosi Species 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
241000233866 Fungi Species 0.000 description 2
241000379510 Heterodera schachtii Species 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
240000008415 Lactuca sativa Species 0.000 description 2
235000003228 Lactuca sativa Nutrition 0.000 description 2
241001143352 Meloidogyne Species 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000008187 granular material Substances 0.000 description 2
229910000041 hydrogen chloride Inorganic materials 0.000 description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
239000011707 mineral Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000000725 suspension Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
JOXBFDPBVQGJOJ-UHFFFAOYSA-N 2,5-dichloro-1,3-benzoxazole Chemical compound ClC1=CC=C2OC(Cl)=NC2=C1 JOXBFDPBVQGJOJ-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
BRENVJPPZRBCPU-UHFFFAOYSA-N 2-chloro-5-methoxy-1,3-benzoxazole Chemical compound COC1=CC=C2OC(Cl)=NC2=C1 BRENVJPPZRBCPU-UHFFFAOYSA-N 0.000 description 1
AVJUFHRBOJNDFG-UHFFFAOYSA-N 2-chloro-5-methyl-1,3-benzoxazole Chemical compound CC1=CC=C2OC(Cl)=NC2=C1 AVJUFHRBOJNDFG-UHFFFAOYSA-N 0.000 description 1
HGRFPWOESXFYDR-UHFFFAOYSA-N 2-chloro-5-propan-2-yl-1,3-benzoxazole Chemical compound CC(C)C1=CC=C2OC(Cl)=NC2=C1 HGRFPWOESXFYDR-UHFFFAOYSA-N 0.000 description 1
FLFWJIBUZQARMD-UHFFFAOYSA-N 2-mercapto-1,3-benzoxazole Chemical compound C1=CC=C2OC(S)=NC2=C1 FLFWJIBUZQARMD-UHFFFAOYSA-N 0.000 description 1
MSZMZTZSFPXXAC-UHFFFAOYSA-N 5,7-dichloro-3h-1,3-benzoxazole-2-thione Chemical compound ClC1=CC(Cl)=C2OC(=S)NC2=C1 MSZMZTZSFPXXAC-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
YAAOMYRRXGGRAZ-UHFFFAOYSA-N 5-bromo-2-chloro-1,3-benzoxazole Chemical compound BrC1=CC=C2OC(Cl)=NC2=C1 YAAOMYRRXGGRAZ-UHFFFAOYSA-N 0.000 description 1
241000294569 Aphelenchoides Species 0.000 description 1
241000134843 Aphelenchoides besseyi Species 0.000 description 1
241000294568 Aphelenchoides fragariae Species 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
206010011732 Cyst Diseases 0.000 description 1
241000399934 Ditylenchus Species 0.000 description 1
241000399949 Ditylenchus dipsaci Species 0.000 description 1
235000016623 Fragaria vesca Nutrition 0.000 description 1
240000009088 Fragaria x ananassa Species 0.000 description 1
235000011363 Fragaria x ananassa Nutrition 0.000 description 1
241000223218 Fusarium Species 0.000 description 1
241000223194 Fusarium culmorum Species 0.000 description 1
241000427940 Fusarium solani Species 0.000 description 1
241001480224 Heterodera Species 0.000 description 1
241000243784 Meloidogyne arenaria Species 0.000 description 1
241000243786 Meloidogyne incognita Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
241001148650 Paratylenchus Species 0.000 description 1
241001149949 Phytophthora cactorum Species 0.000 description 1
241000201377 Radopholus Species 0.000 description 1
241000855013 Rotylenchus Species 0.000 description 1
241000221696 Sclerotinia sclerotiorum Species 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
241000561282 Thielaviopsis basicola Species 0.000 description 1
241000201423 Xiphinema Species 0.000 description 1
IQLPGLICPZNTPK-UHFFFAOYSA-N [P].OS(Cl)(=O)=O Chemical compound [P].OS(Cl)(=O)=O IQLPGLICPZNTPK-UHFFFAOYSA-N 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
208000031513 cyst Diseases 0.000 description 1
230000006378 damage Effects 0.000 description 1
239000000645 desinfectant Substances 0.000 description 1
230000007717 exclusion Effects 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000007952 growth promoter Substances 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
231100001225 mammalian toxicity Toxicity 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
239000006072 paste Substances 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
150000004760 silicates Chemical class 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
238000001228 spectrum Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003892 spreading Methods 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

IL23253A 1964-04-29 1965-03-30 Soil treatment compositions containing a 2-chloro-benzoxazole IL23253A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DEF42750A DE1210617B (de)	1964-04-29	1964-04-29	Bodenbehandlungsmittel

Publications (1)

Publication Number	Publication Date
IL23253A true IL23253A (en)	1968-08-22

Family

ID=7099236

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL23253A IL23253A (en)	1964-04-29	1965-03-30	Soil treatment compositions containing a 2-chloro-benzoxazole

Country Status (10)

Country	Link
US (1)	US3284294A (de)
BE (1)	BE663153A (de)
BR (1)	BR6569234D0 (de)
CH (1)	CH451591A (de)
DE (1)	DE1210617B (de)
FR (1)	FR1455099A (de)
GB (1)	GB1036580A (de)
IL (1)	IL23253A (de)
MY (1)	MY6700021A (de)
NL (1)	NL6505511A (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3520898A (en) *	1967-08-24	1970-07-21	Monsanto Chem Australia Ltd	2-trichloro-methylbenzoxazoles
US4433153A (en) *	1981-07-07	1984-02-21	Hoechst Aktiengesellschaft	Process for the manufacture of 2,6-dichlorobenzoxazole and 2,6-dichlorobenzthiazole
DE3207153A1 (de) *	1982-02-27	1983-09-08	Cassella Ag, 6000 Frankfurt	Verfahren zur herstellung von 2-chlorbenzoxazolen
DE3334417A1 (de) *	1983-09-23	1985-04-04	Cassella Ag, 6000 Frankfurt	Verfahren zur herstellung von 2-chlorbenzoxazolen
DE3406909A1 (de) *	1984-02-25	1985-09-05	Hoechst Ag, 6230 Frankfurt	Verfahren zur herstellung von 2,6-dichlorbenzoxazol
EP0626379B1 (de) *	1993-04-27	2001-03-21	Bayer Ag	Verfahren zur Herstellung von 2-Chlor-benzothiazolen oder 2-Chlor-benzoxazolen

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE613172C (de) *	1933-10-28	1935-05-13	I G Farbenindustrie Akt Ges	Verfahren zur Darstellung von Kondensationsprodukten der Oxazolreihe
US2429178A (en) *	1944-03-10	1947-10-14	Alfred W Anish	Benzoxazoles and method of preparation
US2969370A (en) *	1957-02-14	1961-01-24	Dow Chemical Co	Process for the preparation of 2-amino-5-chlorobenzoxazole

1964
- 1964-04-29 DE DEF42750A patent/DE1210617B/de active Pending
1965
- 1965-03-29 CH CH428165A patent/CH451591A/de unknown
- 1965-03-30 IL IL23253A patent/IL23253A/en unknown
- 1965-04-02 GB GB14054/65A patent/GB1036580A/en not_active Expired
- 1965-04-26 US US451072A patent/US3284294A/en not_active Expired - Lifetime
- 1965-04-27 BR BR169234/65A patent/BR6569234D0/pt unknown
- 1965-04-28 BE BE663153D patent/BE663153A/xx unknown
- 1965-04-29 NL NL6505511A patent/NL6505511A/xx unknown
- 1965-04-29 FR FR15225A patent/FR1455099A/fr not_active Expired
1967
- 1967-12-31 MY MY196721A patent/MY6700021A/xx unknown

Also Published As

Publication number	Publication date
NL6505511A (de)	1965-11-01
DE1210617B (de)	1966-02-10
US3284294A (en)	1966-11-08
FR1455099A (fr)	1966-04-01
MY6700021A (de)	1967-12-31
CH451591A (de)	1968-05-15
BR6569234D0 (pt)	1973-08-14
GB1036580A (en)	1966-07-20
BE663153A (de)	1965-10-28

Publication	Publication Date	Title
EP0454621B1 (de)	2000-07-12	Nematizide Mittel
US3344153A (en)	1967-09-26	Acylated sulphenic acid amides and process for their production
US2553777A (en)	1951-05-22	Parasiticidal compositions containing substituted dithiotrichloro methanes
US3412149A (en)	1968-11-19	Phenyl-mercaptomethane-sulfonamide
US2893911A (en)	1959-07-07	1, 2-bis(alkylsulfoxy)-1, 2-dihaloethylenes and fungicidal compositions comprising them
IL23253A (en)	1968-08-22	Soil treatment compositions containing a 2-chloro-benzoxazole
EP0217747B1 (de)	1991-11-21	Nematizide Mittel
DE1193495B (de)	1965-05-26	Verfahren zur Herstellung von als Schaedlings-bekaempfungsmittel geeigneten halogensubstituierten AEthenylsulfonen
KR900004697B1 (ko)	1990-07-02	2-(3-피리딜)-1,3,4-옥사디아졸류의 제조방법
EP0364396A1 (de)	1990-04-18	Nematizide und fungizide Mittel
US3395231A (en)	1968-07-30	Soil-borne nematode control by seeds treated with 2-chloro-4-halophenyl esters of alkoxyethanesulfonic acids
EP0285565B1 (de)	1993-09-15	2-Mercapto-5-pyridyl-1,3,4-oxadiazole und -1,3,4-thiadiazole, Verfahren zu ihrer Herstellung und ihre Verwendung als nematizide Mittel
EP0290379A2 (de)	1988-11-09	2-Mercapto-5-pyrazinyl-1,3,4-oxadiazole und -1,3,4-thiadiazole, Verfahren zu ihrer Herstellung und ihre Verwendung als nematizide Mittel
US3256147A (en)	1966-06-14	N-nitroso-n-lower alkyl-haloanilines as nematocides
EP0321408B1 (de)	1992-09-23	2-Thio-5-difluoromethylthio-1,3,4-thiadiazole und diese enthaltende nematizide Mittel
IL25831A (en)	1970-02-19	Nematocidal compositions containing esters of o-ethyl-s,s-dipropyl-dithiolphosphoric acid
US2402016A (en)	1946-06-11	Sulphonium salts
EP0263066A2 (de)	1988-04-06	2-Mercapto-oxadiazol- und -thiadiazol-Derivate, Verfahren zu ihrer Herstellung und diese enthaltende nematizide Mittel
US3293276A (en)	1966-12-20	Process for the production of isothiocyanates
US2795525A (en)	1957-06-11	Method of eradicating nematodes by applying thereto sulfenyl xanthates
US3039918A (en)	1962-06-19	Agents for combating plant injuring nematodes
US2287249A (en)	1942-06-23	Chlorine derivatives of benzyl phenyl ether
EP0364395A1 (de)	1990-04-18	Nematizide Mittel
IL23691A (en)	1968-11-27	Amidothiolphosphoric acid esters and process for the preparation thereof
US3284288A (en)	1966-11-08	Pesticides and production thereof