NO117670B - - Google Patents

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Info

Publication number: NO117670B
Authority: NO; Norway
Prior art keywords: compounds; preparation; lower alkyl; substituted; nitro
Prior art date: 1965-07-13

Application number

NO16388266A

Other languages

English (en)

Norwegian (no)

Inventor

G Newbold

A Percival

Original Assignee

Fisons Pest Control Ltd

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.)

1965-07-13

Filing date

1966-07-11

Publication date

1969-09-08

1966-07-11 Application filed by Fisons Pest Control Ltd filed Critical Fisons Pest Control Ltd

1969-09-08 Publication of NO117670B publication Critical patent/NO117670B/no

Links

238000002360 preparation method Methods 0.000 claims description 13
125000000217 alkyl group Chemical group 0.000 claims description 7
230000000749 insecticidal effect Effects 0.000 claims description 6
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
239000001301 oxygen Substances 0.000 claims description 5
229910052760 oxygen Inorganic materials 0.000 claims description 5
239000000460 chlorine Substances 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
150000003839 salts Chemical class 0.000 claims description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
239000005864 Sulphur Substances 0.000 claims description 3
239000004480 active ingredient Substances 0.000 claims description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
229910052794 bromium Inorganic materials 0.000 claims description 3
125000003342 alkenyl group Chemical group 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 claims 1
150000001875 compounds Chemical class 0.000 description 18
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
-1 nitro, cyan, amino Chemical group 0.000 description 8
150000001556 benzimidazoles Chemical class 0.000 description 7
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
238000002474 experimental method Methods 0.000 description 6
230000000694 effects Effects 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
238000009736 wetting Methods 0.000 description 5
239000002917 insecticide Substances 0.000 description 4
239000000047 product Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
241001124076 Aphididae Species 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
241000255969 Pieris brassicae Species 0.000 description 3
239000002585 base Substances 0.000 description 3
239000003701 inert diluent Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 2
241000255925 Diptera Species 0.000 description 2
241000196324 Embryophyta Species 0.000 description 2
241000238631 Hexapoda Species 0.000 description 2
241000171293 Megoura viciae Species 0.000 description 2
SUZRRICLUFMAQD-UHFFFAOYSA-N N-Methyltaurine Chemical compound CNCCS(O)(=O)=O SUZRRICLUFMAQD-UHFFFAOYSA-N 0.000 description 2
241001606077 Tatochila autodice Species 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
239000011521 glass Substances 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
235000000346 sugar Nutrition 0.000 description 2
150000003871 sulfonates Chemical class 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
CBQDTCDOVVBGMN-UHFFFAOYSA-N 2-methyl-3-octylphenol Chemical compound CCCCCCCCC1=CC=CC(O)=C1C CBQDTCDOVVBGMN-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
BXCSXZJKEJQDKS-UHFFFAOYSA-N 4,5,6-trichloro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound ClC1=C(Cl)C=C2NC(C(F)(F)F)=NC2=C1Cl BXCSXZJKEJQDKS-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
240000007124 Brassica oleracea Species 0.000 description 1
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
244000178937 Brassica oleracea var. capitata Species 0.000 description 1
LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
239000005574 MCPA Substances 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
108010009736 Protein Hydrolysates Proteins 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
241000219873 Vicia Species 0.000 description 1
239000002253 acid Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001449 anionic compounds Chemical class 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
239000003139 biocide Substances 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
238000009835 boiling Methods 0.000 description 1
JIJAYWGYIDJVJI-UHFFFAOYSA-N butyl naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)OCCCC)=CC=CC2=C1 JIJAYWGYIDJVJI-UHFFFAOYSA-N 0.000 description 1
239000000969 carrier Substances 0.000 description 1
150000001767 cationic compounds Chemical class 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
150000002194 fatty esters Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000007429 general method Methods 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
239000002418 insect attractant Substances 0.000 description 1
150000008040 ionic compounds Chemical class 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
239000000463 material Substances 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
230000003020 moisturizing effect Effects 0.000 description 1
235000013379 molasses Nutrition 0.000 description 1
125000006682 monohaloalkyl group Chemical group 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
CBFCDTFDPHXCNY-UHFFFAOYSA-N octyldodecane Natural products CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000000123 paper Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
125000006684 polyhaloalkyl group Chemical group 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000000843 powder Substances 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
239000003531 protein hydrolysate Substances 0.000 description 1
239000004576 sand Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 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
150000008163 sugars Chemical class 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000002966 varnish Substances 0.000 description 1
238000009423 ventilation Methods 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000002759 woven fabric Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/10—Radicals substituted by halogen atoms or nitro radicals
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/50—Treatment of water, waste water, or sewage by addition or application of a germicide or by oligodynamic treatment

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Hydrology & Water Resources (AREA)
Engineering & Computer Science (AREA)
Environmental & Geological Engineering (AREA)
Water Supply & Treatment (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)

NO16388266A 1965-07-13 1966-07-11 NO117670B (de)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
GB2958365		1965-07-13
GB3241465A GB1151424A (en)	1965-07-13	1965-07-13	Benzimidazoles and compositions thereof
GB3241365		1965-07-29

Publications (1)

Publication Number	Publication Date
NO117670B true NO117670B (de)	1969-09-08

Family

ID=27258827

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO16388266A NO117670B (de)	1965-07-13	1966-07-11

Country Status (12)

Country	Link
AT (3)	AT267519B (de)
BE (1)	BE683810A (de)
BR (1)	BR6680829D0 (de)
CH (1)	CH459654A (de)
DE (1)	DE1670717A1 (de)
ES (1)	ES329012A1 (de)
FR (1)	FR1503580A (de)
GB (1)	GB1151424A (de)
IL (1)	IL26042A (de)
LU (1)	LU51494A1 (de)
NL (1)	NL6609819A (de)
NO (1)	NO117670B (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3625954A (en) *	1968-03-20	1971-12-07	Pfizer	1-aroylbenzimidazoles
HU164653B (de) *	1971-07-23	1974-03-28
CN115477615B (zh) *	2022-10-17	2024-06-18	黄山学院	N-(3-(苯并咪唑-2-基)苯基)酰胺类化合物及其制备方法和应用

1965
- 1965-07-13 GB GB3241465A patent/GB1151424A/en not_active Expired
1966
- 1966-06-27 IL IL2604266A patent/IL26042A/xx unknown
- 1966-06-30 BR BR18082966A patent/BR6680829D0/pt unknown
- 1966-07-06 LU LU51494A patent/LU51494A1/xx unknown
- 1966-07-07 BE BE683810D patent/BE683810A/xx unknown
- 1966-07-08 CH CH992066A patent/CH459654A/fr unknown
- 1966-07-11 DE DE19661670717 patent/DE1670717A1/de active Pending
- 1966-07-11 AT AT663066A patent/AT267519B/de active
- 1966-07-11 AT AT804167A patent/AT272759B/de active
- 1966-07-11 AT AT804067A patent/AT275234B/de active
- 1966-07-11 NO NO16388266A patent/NO117670B/no unknown
- 1966-07-12 ES ES329012A patent/ES329012A1/es not_active Expired
- 1966-07-13 FR FR69329A patent/FR1503580A/fr not_active Expired
- 1966-07-13 NL NL6609819A patent/NL6609819A/xx unknown

Also Published As

Publication number	Publication date
LU51494A1 (de)	1967-01-06
BE683810A (de)	1967-01-09
AT275234B (de)	1969-10-10
BR6680829D0 (pt)	1973-12-26
NL6609819A (de)	1967-01-16
CH459654A (fr)	1968-07-15
IL26042A (en)	1970-12-24
ES329012A1 (es)	1968-03-01
AT267519B (de)	1969-01-10
FR1503580A (fr)	1967-12-01
DE1670717A1 (de)	1970-12-03
AT272759B (de)	1969-07-25
GB1151424A (en)	1969-05-07

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NO163882B (no)	1990-04-30	Produkt for absorpsjon av kroppsvaesker.
DE69217085T2 (de)	1997-05-28	Insekttötende phenylhydrazin-derivate
JP2739738B2 (ja)	1998-04-15	置換ベンゾイル誘導体および選択性除草剤
JPS63174907A (ja)	1988-07-19	シロアリの駆除方法
GB2119650A (en)	1983-11-23	Antiviral isothiosemicarbazones
DE2949138C2 (de)	1991-03-14
JPS605585B2 (ja)	1985-02-12	２，５′−ビストリフルオロメチル−２′−クロル−４，６−ジニトロジフェニルアミンおよびその製造方法ならびに該化合物を活性成分とする殺虫剤，殺ダニ剤または殺菌剤組成物
JPS6012322B2 (ja)	1985-04-01	作物保護剤
DE2948095A1 (de)	1981-06-19	Phenoxialkan- und phenoxialkencarbonsaeuren und deren derivate, ihre herstellung und verwendung
US3721678A (en)	1973-03-20	2-trifluoromethyl-or 2-pentafluoroethylbenzimidazole
US4251545A (en)	1981-02-17	Fungicidal process using 1-(alkoxyaroyl)guanidines
SU741773A3 (ru)	1980-06-15	Акарицидный состав
JPH0421672B2 (de)	1992-04-13
HU184822B (en)	1984-10-29	Insecticide and nematocide compositions containing asymmetric thiophosphonates
HU187698B (en)	1986-02-28	Insecticidnye kompositions containing pyrazoline derivatives further process for preparing the pyrazoline derivatives
US5089510A (en)	1992-02-18	Insecticides
US4067896A (en)	1978-01-10	(Isothiocyanato-methoxy) biphenyls
JPS6270364A (ja)	1987-03-31	イミダゾ−ル、それらの調製方法およびそれらの殺菌剤としての用途
US3471612A (en)	1969-10-07	Diphenylalkylamines as a hematocide
US3920844A (en)	1975-11-18	Chlorinated diaromatic-substituted aminoalkanes as fungicides and insecticides
US4879314A (en)	1989-11-07	Dihaloformaldoxime
US6423730B1 (en)	2002-07-23	Method to control termites
CA1203812A (en)	1986-04-29	Sulfone and process for its preparation
EP0008854B1 (de)	1983-03-09	Pentadienonhydrazon und dessen Verwendung als Insektizid
DE2049694C3 (de)	1980-02-21	Thiolphosphorsäurenaphtholester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Fungizide