NL7905856A - Nieuwe 5-jood-3-nitro-4-hydroxybenzonitrilzouten en preparaten, die deze zouten bevatten. - Google Patents

Nieuwe 5-jood-3-nitro-4-hydroxybenzonitrilzouten en preparaten, die deze zouten bevatten. Download PDF

Info

Publication number: NL7905856A
Authority: NL; Netherlands
Prior art keywords: salts; salt; general formula; preparation; treatment
Prior art date: 1978-08-04

Application number

NL7905856A

Other languages

English (en)

Dutch (nl)

Original Assignee

Chinoin Gyogyszer Es Vegyeszet

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.)

1978-08-04

Filing date

1979-07-30

Publication date

1980-02-06

1979-07-30 Application filed by Chinoin Gyogyszer Es Vegyeszet filed Critical Chinoin Gyogyszer Es Vegyeszet

1980-02-06 Publication of NL7905856A publication Critical patent/NL7905856A/nl

Links

150000003839 salts Chemical class 0.000 title claims description 35
238000002360 preparation method Methods 0.000 title claims description 27
239000000203 mixture Substances 0.000 claims description 13
SGKGVABHDAQAJO-UHFFFAOYSA-N nitroxynil Chemical compound OC1=C(I)C=C(C#N)C=C1[N+]([O-])=O SGKGVABHDAQAJO-UHFFFAOYSA-N 0.000 claims description 12
238000000034 method Methods 0.000 claims description 10
239000003795 chemical substances by application Substances 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 8
239000001257 hydrogen Substances 0.000 claims description 8
239000002904 solvent Substances 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 7
239000003085 diluting agent Substances 0.000 claims description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
239000013543 active substance Substances 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
125000003545 alkoxy group Chemical group 0.000 claims description 5
239000000969 carrier Substances 0.000 claims description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
239000000654 additive Substances 0.000 claims description 4
150000001875 compounds Chemical class 0.000 claims description 4
238000002347 injection Methods 0.000 claims description 4
239000007924 injection Substances 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
239000000126 substance Substances 0.000 claims description 4
239000004606 Fillers/Extenders Substances 0.000 claims description 3
OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 claims description 3
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 3
239000000853 adhesive Substances 0.000 claims description 2
230000001070 adhesive effect Effects 0.000 claims description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
239000003995 emulsifying agent Substances 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims description 2
125000001624 naphthyl group Chemical group 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
239000000080 wetting agent Substances 0.000 claims description 2
241001465754 Metazoa Species 0.000 claims 3
150000001409 amidines Chemical class 0.000 claims 1
230000015572 biosynthetic process Effects 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
239000000825 pharmaceutical preparation Substances 0.000 claims 1
DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 claims 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
239000011253 protective coating Substances 0.000 claims 1
230000007306 turnover Effects 0.000 claims 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
239000000243 solution Substances 0.000 description 13
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
-1 amidine compound Chemical class 0.000 description 4
IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical class OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000013078 crystal Substances 0.000 description 3
230000008018 melting Effects 0.000 description 3
238000002844 melting Methods 0.000 description 3
239000011877 solvent mixture Substances 0.000 description 3
241000283690 Bos taurus Species 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
241000242711 Fasciola hepatica Species 0.000 description 2
239000004480 active ingredient Substances 0.000 description 2
239000003125 aqueous solvent Substances 0.000 description 2
230000004071 biological effect Effects 0.000 description 2
229910000019 calcium carbonate Inorganic materials 0.000 description 2
230000000694 effects Effects 0.000 description 2
208000006275 fascioliasis Diseases 0.000 description 2
230000002349 favourable effect Effects 0.000 description 2
238000009472 formulation Methods 0.000 description 2
210000004185 liver Anatomy 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
DVNYTAVYBRSTGK-UHFFFAOYSA-N Aminoimidazole carboxamide Natural products NC(=O)C=1N=CNC=1N DVNYTAVYBRSTGK-UHFFFAOYSA-N 0.000 description 1
208000031295 Animal disease Diseases 0.000 description 1
241000283986 Lepus Species 0.000 description 1
241001494479 Pecora Species 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
230000000507 anthelmentic effect Effects 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
239000003124 biologic agent Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229910000281 calcium bentonite Inorganic materials 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
230000008021 deposition Effects 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
239000008187 granular material Substances 0.000 description 1
230000035876 healing Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
239000005457 ice water Substances 0.000 description 1
239000011256 inorganic filler Substances 0.000 description 1
229910003475 inorganic filler Inorganic materials 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
208000019423 liver disease Diseases 0.000 description 1
PBYJDHRFPFHVKZ-UHFFFAOYSA-N n,n-dibutyl-4-hexoxynaphthalene-1-carboximidamide;hydrochloride Chemical compound Cl.C1=CC=C2C(OCCCCCC)=CC=C(C(=N)N(CCCC)CCCC)C2=C1 PBYJDHRFPFHVKZ-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000006610 n-decyloxy group Chemical group 0.000 description 1
210000004237 neck muscle Anatomy 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Substances 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
230000008635 plant growth Effects 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
238000000746 purification Methods 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
230000028327 secretion Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000725 suspension Substances 0.000 description 1
208000024891 symptom Diseases 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/52—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing groups, e.g. carboxylic acid amidines
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
- C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Dentistry (AREA)
Environmental Sciences (AREA)
Zoology (AREA)
Wood Science & Technology (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Veterinary Medicine (AREA)
Agronomy & Crop Science (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Animal Behavior & Ethology (AREA)
Chemical Kinetics & Catalysis (AREA)
Pharmacology & Pharmacy (AREA)
Tropical Medicine & Parasitology (AREA)
General Chemical & Material Sciences (AREA)
Public Health (AREA)
Medicinal Chemistry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicinal Preparation (AREA)

NL7905856A 1978-08-04 1979-07-30 Nieuwe 5-jood-3-nitro-4-hydroxybenzonitrilzouten en preparaten, die deze zouten bevatten. NL7905856A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
HU78CI1851A HU179947B (en)	1978-08-04	1978-08-04	Process for preparing substituted 4-hydroxy-benzonitrile salts
HUCI001851		1978-08-04

Publications (1)

Publication Number	Publication Date
NL7905856A true NL7905856A (nl)	1980-02-06

Family

ID=10994704

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL7905856A NL7905856A (nl)	1978-08-04	1979-07-30	Nieuwe 5-jood-3-nitro-4-hydroxybenzonitrilzouten en preparaten, die deze zouten bevatten.

Country Status (15)

Country	Link
JP (1)	JPS5524169A (fr)
BE (1)	BE878013A (fr)
DE (1)	DE2928291A1 (fr)
DK (1)	DK328379A (fr)
ES (1)	ES483822A1 (fr)
FI (1)	FI792403A7 (fr)
FR (1)	FR2432505B1 (fr)
GB (1)	GB2027020B (fr)
GR (1)	GR69932B (fr)
HU (1)	HU179947B (fr)
IT (1)	IT1121011B (fr)
NL (1)	NL7905856A (fr)
NO (1)	NO151283C (fr)
SE (1)	SE7906504L (fr)
SU (1)	SU852168A3 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4919409A (en) *	1986-07-03	1990-04-24	Xerox Corporation	Sheet handling apparatus with narrow belt having raised frictional contact element

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR840429A (fr) *	1937-07-08	1939-04-25	Geigy Ag J R	Composés azotés solubles dans l'eau et leur procédé de fabrication
US3694556A (en) *	1963-03-22	1972-09-26	Burroughs Wellcome Co	Anti-tapeworm infection composition
US3326658A (en) *	1964-01-28	1967-06-20	Schering Corp	Method for controlling plant growth
GB1104885A (en) *	1964-12-18	1968-03-06	May & Baker Ltd	Method for the treatment of helminth infestations
CH478522A (de) *	1966-07-05	1969-09-30	Ciba Geigy	Mittel gegen Ektoparasiten auf Tieren

1978
- 1978-08-04 HU HU78CI1851A patent/HU179947B/hu unknown
1979
- 1979-07-13 DE DE19792928291 patent/DE2928291A1/de not_active Withdrawn
- 1979-07-18 GB GB7925065A patent/GB2027020B/en not_active Expired
- 1979-07-19 IT IT68497/79A patent/IT1121011B/it active
- 1979-07-30 NL NL7905856A patent/NL7905856A/nl not_active Application Discontinuation
- 1979-07-31 SE SE7906504A patent/SE7906504L/xx not_active Application Discontinuation
- 1979-08-01 FI FI792403A patent/FI792403A7/fi not_active Application Discontinuation
- 1979-08-01 BE BE0/196553A patent/BE878013A/fr not_active IP Right Cessation
- 1979-08-01 ES ES483822A patent/ES483822A1/es not_active Expired
- 1979-08-02 FR FR7919853A patent/FR2432505B1/fr not_active Expired
- 1979-08-03 JP JP9878479A patent/JPS5524169A/ja active Pending
- 1979-08-03 DK DK328379A patent/DK328379A/da not_active Application Discontinuation
- 1979-08-03 SU SU792792451A patent/SU852168A3/ru active
- 1979-08-03 NO NO792569A patent/NO151283C/no unknown
- 1979-08-03 GR GR59767A patent/GR69932B/el unknown

Also Published As

Publication number	Publication date
JPS5524169A (en)	1980-02-21
DK328379A (da)	1980-03-05
GR69932B (fr)	1982-07-21
DE2928291A1 (de)	1980-02-28
IT1121011B (it)	1986-03-26
NO151283C (no)	1985-03-13
ES483822A1 (es)	1980-04-16
NO151283B (no)	1984-12-03
GB2027020B (en)	1982-11-10
FI792403A7 (fi)	1980-02-05
IT7968497A0 (it)	1979-07-19
FR2432505A1 (fr)	1980-02-29
SU852168A3 (ru)	1981-07-30
HU179947B (en)	1983-01-28
GB2027020A (en)	1980-02-13
FR2432505B1 (fr)	1985-07-12
SE7906504L (sv)	1980-02-05
NO792569L (no)	1980-02-05
BE878013A (fr)	1979-12-03

Legal Events

Date	Code	Title	Description
1985-01-01	A85	Still pending on 85-01-01
1986-09-01	BV	The patent application has lapsed

Publication	Publication Date	Title
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
JPS6141353B2 (fr)	1986-09-13
RU2040179C1 (ru)	1995-07-25	Синергетический гербицидный состав и способ борьбы с нежелательной растительностью
IL31204A (en)	1972-09-28	Isoxazolyl carbamates and compositions containing them
NL7905856A (nl)	1980-02-06	Nieuwe 5-jood-3-nitro-4-hydroxybenzonitrilzouten en preparaten, die deze zouten bevatten.
JP3488890B2 (ja)	2004-01-19	３−ｎ−置換キナゾリノン誘導体、その製造法および該化合物を含有する除草剤
JPH04120007A (ja)	1992-04-21	殺虫組成物
RU2236134C1 (ru)	2004-09-20	Гербицидный состав для борьбы с нежелательной растительностью в посевах зерновых культур
JPH07103079B2 (ja)	1995-11-08	パラアリールオキシアラルキルアミン誘導体および殺虫・殺ダニ剤
KR880002603B1 (ko)	1988-12-04	페녹시알킬아마이드 유도체의 제조방법
JPS60214785A (ja)	1985-10-28	ピラゾ−ルスルホニルウレア誘導体、および植物生長調節剤または除草剤
US3113968A (en)	1963-12-10	1-phenyl, 1-hydroxyalkyl, 3, 3-dialkyl-ureas
US3399199A (en)	1968-08-27	Nitroalkyl-piperazines
PT99616B (pt)	1999-05-31	Processo para a preparacao de compostos diarilpirrolecarbonitrilo e diarilnitropirrole insecticidas e acaricidas
IL31205A (en)	1972-12-29	(thiono)carbamates of dithiacycloheptanone-oxime
US3678168A (en)	1972-07-18	Nitroalkyl-piperazines for inhibiting bacteria fungi and nematodes
RS51570B (sr)	2011-08-31	Postupak za kontrolisanje korova
JPH0143732B2 (fr)	1989-09-22
US4125617A (en)	1978-11-14	Acaricidal pyridinium salts
KR830001714B1 (ko)	1983-08-31	디페닐 에테르 유도체의 제조방법
US3475447A (en)	1969-10-28	N,n-disubstituted benzimidazole - 2-carbonamidines and a process for their preparation
JPS6111948B2 (fr)	1986-04-05
KR810001244B1 (ko)	1981-09-30	디페닐에테르 유도체의 제조방법
JPH0570311A (ja)	1993-03-23	除草組成物
JPH08268811A (ja)	1996-10-15	除草剤