IL36677A - 3,4,5-trialkylcyclohexanols,their preparation and their use as fungicides - Google Patents

3,4,5-trialkylcyclohexanols,their preparation and their use as fungicides

Info

Publication number: IL36677A
Authority: IL; Israel
Prior art keywords: compound; compositions; carrier; composition; fungicidal
Prior art date: 1970-04-28

Application number

IL36677A

Other languages

English (en)

Other versions

IL36677A0 (en

Original Assignee

Exxon Research Engineering Co

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.)

1970-04-28

Filing date

1971-04-21

Publication date

1973-11-28

1971-04-21 Application filed by Exxon Research Engineering Co filed Critical Exxon Research Engineering Co

1971-06-23 Publication of IL36677A0 publication Critical patent/IL36677A0/xx

1973-11-28 Publication of IL36677A publication Critical patent/IL36677A/en

Links

239000000417 fungicide Substances 0.000 title description 7
238000002360 preparation method Methods 0.000 title description 2
239000000203 mixture Substances 0.000 claims description 40
150000001875 compounds Chemical class 0.000 claims description 20
230000000855 fungicidal effect Effects 0.000 claims description 17
239000007788 liquid Substances 0.000 claims description 11
239000007787 solid Substances 0.000 claims description 11
239000002904 solvent Substances 0.000 claims description 11
238000000034 method Methods 0.000 claims description 9
239000003085 diluting agent Substances 0.000 claims description 6
230000002538 fungal effect Effects 0.000 claims description 6
239000003208 petroleum Substances 0.000 claims description 6
241000233866 Fungi Species 0.000 claims description 5
206010061217 Infestation Diseases 0.000 claims description 5
NFZFYGGERZUDFK-UHFFFAOYSA-N 3,4,5-trimethylcyclohexan-1-ol Chemical compound CC1CC(O)CC(C)C1C NFZFYGGERZUDFK-UHFFFAOYSA-N 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
239000004480 active ingredient Substances 0.000 description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
239000002270 dispersing agent Substances 0.000 description 9
239000007921 spray Substances 0.000 description 9
239000000969 carrier Substances 0.000 description 8
239000000463 material Substances 0.000 description 8
239000000126 substance Substances 0.000 description 8
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
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125000000217 alkyl group Chemical group 0.000 description 2
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230000015572 biosynthetic process Effects 0.000 description 2
238000009835 boiling Methods 0.000 description 2
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159000000007 calcium salts Chemical class 0.000 description 2
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QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
229920005610 lignin Polymers 0.000 description 2
239000011707 mineral Substances 0.000 description 2
235000010755 mineral Nutrition 0.000 description 2
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ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
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125000001424 substituent group Chemical group 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
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239000000454 talc Substances 0.000 description 2
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235000020234 walnut Nutrition 0.000 description 2
PNXWPUCNFMVBBK-UHFFFAOYSA-M 1-dodecylpyridin-1-ium;bromide Chemical compound [Br-].CCCCCCCCCCCC[N+]1=CC=CC=C1 PNXWPUCNFMVBBK-UHFFFAOYSA-M 0.000 description 1
WZUNUACWCJJERC-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CC)(CO)CO WZUNUACWCJJERC-UHFFFAOYSA-N 0.000 description 1
BRRVXFOKWJKTGG-UHFFFAOYSA-N 3,3,5-trimethylcyclohexanol Chemical compound CC1CC(O)CC(C)(C)C1 BRRVXFOKWJKTGG-UHFFFAOYSA-N 0.000 description 1
VULOWDCMYZIKOO-UHFFFAOYSA-N 3,4,5-triethylcyclohexan-1-ol Chemical compound C(C)C1CC(CC(C1CC)CC)O VULOWDCMYZIKOO-UHFFFAOYSA-N 0.000 description 1
HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
UEJJYMUGYWUKDW-UHFFFAOYSA-N 3-ethyl-5-methyl-4-propylcyclohexan-1-ol Chemical compound CC1CC(CC(C1CCC)CC)O UEJJYMUGYWUKDW-UHFFFAOYSA-N 0.000 description 1
IIPPNMBCXZOLTB-UHFFFAOYSA-N 3-ethyl-5-propan-2-yl-4-propylcyclohexan-1-ol Chemical compound C(C)C1CC(CC(C1CCC)C(C)C)O IIPPNMBCXZOLTB-UHFFFAOYSA-N 0.000 description 1
BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
LOWAYJFCOAGQKV-UHFFFAOYSA-N 4-ethyl-3,5-dimethylcyclohexan-1-ol Chemical compound CCC1C(C)CC(O)CC1C LOWAYJFCOAGQKV-UHFFFAOYSA-N 0.000 description 1
SUYOJTKFMWSPNN-UHFFFAOYSA-N 4-methyl-3,5-di(propan-2-yl)cyclohexan-1-ol Chemical compound C(C)(C)C1CC(CC(C1C)C(C)C)O SUYOJTKFMWSPNN-UHFFFAOYSA-N 0.000 description 1
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150000002430 hydrocarbons Chemical class 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
238000011534 incubation Methods 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical group O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
229910052622 kaolinite Inorganic materials 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
230000003902 lesion Effects 0.000 description 1
239000010687 lubricating oil Substances 0.000 description 1
239000011419 magnesium lime Substances 0.000 description 1
239000000594 mannitol Substances 0.000 description 1
235000010355 mannitol Nutrition 0.000 description 1
229960001855 mannitol Drugs 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
NCPHGZWGGANCAY-UHFFFAOYSA-N methane;ruthenium Chemical compound C.[Ru] NCPHGZWGGANCAY-UHFFFAOYSA-N 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 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
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000004200 microcrystalline wax Substances 0.000 description 1
235000019808 microcrystalline wax Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000003607 modifier Substances 0.000 description 1
239000012170 montan wax Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
239000000025 natural resin Substances 0.000 description 1
FCBBRODPXVPZAH-UHFFFAOYSA-N nonan-5-ol Chemical compound CCCCC(O)CCCC FCBBRODPXVPZAH-UHFFFAOYSA-N 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
229910052625 palygorskite Chemical group 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
230000001717 pathogenic effect Effects 0.000 description 1
229910003446 platinum oxide Inorganic materials 0.000 description 1
229920001983 poloxamer Polymers 0.000 description 1
229920001521 polyalkylene glycol ether Polymers 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
229920000223 polyglycerol Polymers 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
229940096992 potassium oleate Drugs 0.000 description 1
MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
238000000746 purification Methods 0.000 description 1
238000006268 reductive amination reaction Methods 0.000 description 1
235000003499 redwood Nutrition 0.000 description 1
238000007670 refining Methods 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
229910052702 rhenium Inorganic materials 0.000 description 1
WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
229910052703 rhodium Inorganic materials 0.000 description 1
239000010948 rhodium Substances 0.000 description 1
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
229910052707 ruthenium Inorganic materials 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000004208 shellac Substances 0.000 description 1
ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
235000013874 shellac Nutrition 0.000 description 1
229940113147 shellac Drugs 0.000 description 1
238000007873 sieving Methods 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229960004029 silicic acid Drugs 0.000 description 1
229960001866 silicon dioxide Drugs 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000010421 standard material Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000002426 superphosphate Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
238000010998 test method Methods 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
231100000167 toxic agent Toxicity 0.000 description 1
239000003440 toxic substance Substances 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
238000011282 treatment Methods 0.000 description 1
SZEMGTQCPRNXEG-UHFFFAOYSA-M trimethyl(octadecyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C SZEMGTQCPRNXEG-UHFFFAOYSA-M 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000001993 wax Substances 0.000 description 1

Classifications

- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/06—Oxygen or sulfur directly attached to a cycloaliphatic ring system
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C35/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C35/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic
- C07C35/08—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic containing a six-membered rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated

Landscapes

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

IL36677A 1970-04-28 1971-04-21 3,4,5-trialkylcyclohexanols,their preparation and their use as fungicides IL36677A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US3272970A	1970-04-28	1970-04-28

Publications (2)

Publication Number	Publication Date
IL36677A0 IL36677A0 (en)	1971-06-23
IL36677A true IL36677A (en)	1973-11-28

Family

ID=21866505

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL36677A IL36677A (en)	1970-04-28	1971-04-21	3,4,5-trialkylcyclohexanols,their preparation and their use as fungicides

Country Status (12)

Country	Link
US (1)	US3689574A (de)
AT (1)	AT309893B (de)
BE (1)	BE766349A (de)
CA (1)	CA965104A (de)
CH (1)	CH551749A (de)
DE (1)	DE2120371A1 (de)
FR (1)	FR2090869A5 (de)
GB (1)	GB1331331A (de)
HU (1)	HU162241B (de)
IL (1)	IL36677A (de)
NL (1)	NL7105720A (de)
SU (1)	SU374777A3 (de)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SI1551372T1 (en)	2002-09-20	2018-08-31	Alpharma Pharmaceuticals Llc	SUBVENCATION DATA AND RELATED CONSTRUCTIONS AND PROCEDURES
CA2472806A1 (en) *	2004-05-18	2005-11-18	Petro-Canada	Compositions and methods for treating turf insect pests and diseases such as fungal infestations
SI2484346T1 (sl)	2006-06-19	2017-05-31	Alpharma Pharmaceuticals Llc	Farmacevtski sestavki
US9357768B2 (en)	2006-10-05	2016-06-07	Suncor Energy Inc.	Herbicidal composition with increased herbicidal efficacy
US8623418B2 (en)	2007-12-17	2014-01-07	Alpharma Pharmaceuticals Llc	Pharmaceutical composition
US8569210B2 (en)	2008-06-26	2013-10-29	Suncor Energy Inc.	Turfgrass fungicide formulation with pigment
EP2613635B1 (de)	2010-09-09	2016-04-06	Suncor Energy Inc.	Synergistisches paraffinöl und boscalid-fungizide
KR20140031966A (ko)	2011-06-03	2014-03-13	선코 에너지 인코포레이티드	진균성 병원균에 의한 작물의 감염을 방제하기 위한 파라핀계 수-중-유 에멀젼
JP2015522554A (ja)	2012-06-04	2015-08-06	サンコー・エナジー・インコーポレーテッド	パラフィン油及び沈降防止剤を含む製剤
AU2020211650B2 (en)	2019-01-25	2025-01-30	Nutrien Ag Solutions (Canada) Inc.	Photosensitizer compounds, methods of manufacture and application to plants
JP7588289B2 (ja)	2019-02-15	2024-11-22	ニュートリエン・エージー・ソリューションズ・（カナダ）・インコーポレイテッド	植物の健康を増進するプロトポルフィリンｉｘ誘導体及びその使用

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2433008A (en) *	1945-05-28	1947-12-23	Gulf Research Development Co	4, 6-di-tertiary-butyl-3-methylcyclo-hexanol
US3121728A (en) *	1960-05-20	1964-02-18	Exxon Research Engineering Co	Production of monocarboxylic acids from large ring alicyclic alcohols
US3323984A (en) *	1963-09-13	1967-06-06	Stauffer Chemical Co	Method and composition for controlling fungi
US3385902A (en) *	1966-11-25	1968-05-28	Shell Oil Co	Production of trimethylphenols

1970
- 1970-04-28 US US32729A patent/US3689574A/en not_active Expired - Lifetime
1971
- 1971-04-16 CA CA110,528A patent/CA965104A/en not_active Expired
- 1971-04-21 IL IL36677A patent/IL36677A/en unknown
- 1971-04-26 DE DE19712120371 patent/DE2120371A1/de active Pending
- 1971-04-26 CH CH607471A patent/CH551749A/de not_active IP Right Cessation
- 1971-04-27 BE BE766349A patent/BE766349A/xx unknown
- 1971-04-27 AT AT360671A patent/AT309893B/de not_active IP Right Cessation
- 1971-04-27 NL NL7105720A patent/NL7105720A/xx unknown
- 1971-04-27 GB GB1167571*[A patent/GB1331331A/en not_active Expired
- 1971-04-27 HU HUEO279A patent/HU162241B/hu unknown
- 1971-04-28 FR FR7115171A patent/FR2090869A5/fr not_active Expired
- 1971-04-28 SU SU1651126A patent/SU374777A3/ru active

Also Published As

Publication number	Publication date
US3689574A (en)	1972-09-05
CH551749A (de)	1974-07-31
FR2090869A5 (de)	1972-01-14
DE2120371A1 (de)	1971-11-11
IL36677A0 (en)	1971-06-23
GB1331331A (en)	1973-09-26
AT309893B (de)	1973-09-10
SU374777A3 (de)	1973-03-20
NL7105720A (de)	1971-11-01
HU162241B (de)	1973-01-29
CA965104A (en)	1975-03-25
BE766349A (fr)	1971-10-27

Publication	Publication Date	Title
US3823161A (en)	1974-07-09	Aminothiophene derivatives
US3689574A (en)	1972-09-05	3,4,5-trimethylcyclohexanol
IL33221A (en)	1973-06-29	Benzothiazole derivatives,preparation thereof and microbiocidal preparations containing them
US2849306A (en)	1958-08-26	Herbicidal method and composition employing aryl pseudoureas
US3780051A (en)	1973-12-18	Certain 2-(thiazol-2-yl)-3,5-dioxo-4-methyl-1,2,4-thiadiazolidines
US3694482A (en)	1972-09-26	Malononitrile oxime derivatives
US3705155A (en)	1972-12-05	1-thiadiazolyl-hexahydro-1,3,5-triazine-2-ones
US3403994A (en)	1968-10-01	Herbicidal method
US2779669A (en)	1957-01-29	Acyl pseudourea herbicidal composition and a method for killing weeds therewith
US2722478A (en)	1955-11-01	Process for using trichloromethyl thiocyanate as a biocide
US3780085A (en)	1973-12-18	Malononitrile oxime derivatives
DE2115318A1 (de)	1971-12-09	Triazine, Verfahren zur Herstellung derselben und deren Verwendung als Her
US3780046A (en)	1973-12-18	Herbicidal n-(2-picolyl) substituted 2,6-dinitroanilines
US3433622A (en)	1969-03-18	Method of defoliating plants with organomercurials
US4324795A (en)	1982-04-13	Acaricidal agents
US3781441A (en)	1973-12-25	Use of 4-chloro-3,5-dinitrobenzene-sulfonamide as a fungicide
US3776936A (en)	1973-12-04	Thiocarbamic acid ester pesticides
US3784574A (en)	1974-01-08	Herbicidal n-furfuryl substituted 2,6-dinitroanilines
US3775402A (en)	1973-11-27	3,5-dinitrosulfanilamides
EP0014999A1 (de)	1980-09-03	Optisch aktive Formen des 4-(3-(p-tert.-Butylphenyl)-2-methyl-propyl)-cis-2,6-dimethyl-morpholins und ihre Salze; Fungizide, die diese Verbindungen enthalten, und Verfahren zu ihrer Herstellung
US3691237A (en)	1972-09-12	N-halo-n-phenyl-n'n'dimethyl formamidinium halides
US2745780A (en)	1956-05-15	Acaricide composition containing 4. 4'-dichlorobenzilic acid esters
US5091400A (en)	1992-02-25	Clathrate compound
US3773782A (en)	1973-11-20	Thiophosphates of acylated 3-amino-2-oxazolidones
US3839010A (en)	1974-10-01	Thiocarbamic acid ester pesticides