DD244058A5 - Pestizide, vorzugsweise insektizide mittel - Google Patents

Pestizide, vorzugsweise insektizide mittel Download PDF

Info

Publication number: DD244058A5
Authority: DD; German Democratic Republic
Prior art keywords: halogen; denotes; group; fluorine; substituted
Prior art date: 1985-03-30

Application number

DD86288443A

Other languages

German (de)

English (en)

Inventor

Toyohiko Kume

Shinichi Tsuboi

Kunihiro Isono

Shoko Sasaki

Yumi Hattori

Original Assignee

��@��@��@��@�K@�Kk��

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.)

1985-03-30

Filing date

1986-03-27

Publication date

1987-03-25

1986-03-27 Application filed by ��@��@��@��@�K@�Kk�� filed Critical ��@��@��@��@�K@�Kk��

1987-03-25 Publication of DD244058A5 publication Critical patent/DD244058A5/de

Links

239000002917 insecticide Substances 0.000 title claims abstract description 10
239000000575 pesticide Substances 0.000 title claims abstract description 6
150000001875 compounds Chemical class 0.000 claims abstract description 46
229940054066 benzamide antipsychotics Drugs 0.000 claims abstract description 13
150000003936 benzamides Chemical class 0.000 claims abstract description 13
241000238631 Hexapoda Species 0.000 claims abstract description 10
239000004606 Fillers/Extenders Substances 0.000 claims abstract description 6
239000004094 surface-active agent Substances 0.000 claims abstract description 5
239000000460 chlorine Substances 0.000 claims description 21
239000000203 mixture Substances 0.000 claims description 19
239000011737 fluorine Substances 0.000 claims description 18
229910052731 fluorine Inorganic materials 0.000 claims description 18
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 15
229910052801 chlorine Inorganic materials 0.000 claims description 15
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238000000034 method Methods 0.000 claims description 12
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125000004432 carbon atom Chemical group C* 0.000 claims description 10
229910052736 halogen Inorganic materials 0.000 claims description 9
125000005843 halogen group Chemical group 0.000 claims description 9
150000002367 halogens Chemical class 0.000 claims description 9
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235000002017 Zea mays subsp mays Nutrition 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
229940072049 amyl acetate Drugs 0.000 description 1
PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000005228 aryl sulfonate group Chemical group 0.000 description 1
238000000889 atomisation Methods 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
239000002585 base Substances 0.000 description 1
125000004190 benzothiazol-2-yl group Chemical group [H]C1=C([H])C([H])=C2N=C(*)SC2=C1[H] 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
238000009395 breeding Methods 0.000 description 1
230000001488 breeding effect Effects 0.000 description 1
150000001649 bromium compounds Chemical class 0.000 description 1
239000001273 butane Substances 0.000 description 1
239000002775 capsule Substances 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
239000013078 crystal Substances 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
HPYNZHMRTTWQTB-UHFFFAOYSA-N dimethylpyridine Natural products CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
238000001914 filtration Methods 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000003630 growth substance Substances 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
229920000126 latex Polymers 0.000 description 1
244000144972 livestock Species 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000004579 marble Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 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
244000005700 microbiome Species 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
229920005615 natural polymer Polymers 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
244000045947 parasite Species 0.000 description 1
239000006072 paste Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
229960003351 prussian blue Drugs 0.000 description 1
239000013225 prussian blue Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000003254 radicals Chemical group 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000779 smoke Substances 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000004575 stone Substances 0.000 description 1
125000000547 substituted alkyl group Chemical group 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
150000003462 sulfoxides Chemical class 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000002023 wood 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles 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
- C07D277/82—Nitrogen atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

DD86288443A 1985-03-30 1986-03-27 Pestizide, vorzugsweise insektizide mittel DD244058A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP60065018A JPS61225168A (ja)	1985-03-30	1985-03-30	新規ベンズアミド、その製法及び殺虫剤

Publications (1)

Publication Number	Publication Date
DD244058A5 true DD244058A5 (de)	1987-03-25

Family

ID=13274814

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD86288443A DD244058A5 (de)	1985-03-30	1986-03-27	Pestizide, vorzugsweise insektizide mittel

Country Status (15)

Country	Link
US (1)	US4675331A (da)
EP (1)	EP0196547A1 (da)
JP (1)	JPS61225168A (da)
KR (1)	KR860007231A (da)
CN (1)	CN86102102A (da)
AU (1)	AU5533186A (da)
BR (1)	BR8601372A (da)
DD (1)	DD244058A5 (da)
DK (1)	DK143186A (da)
ES (1)	ES8706137A1 (da)
GR (1)	GR860826B (da)
HU (1)	HUT41229A (da)
IL (1)	IL78282A0 (da)
PH (1)	PH21114A (da)
ZA (1)	ZA862323B (da)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0261459A3 (de) *	1986-09-09	1988-05-11	Nihon Tokushu Noyaku Seizo K.K.	Neue N-Benzothiazolylamide
IL90337A0 (en) *	1988-05-24	1989-12-15	Pfizer	Aromatic and heterocyclic carboxamide derivatives as antineoplastic agents
US4874864A (en) *	1988-05-24	1989-10-17	Pfizer Inc.	Benzamide protease inhibitors
FR2674524B1 (fr) *	1991-03-25	1993-05-21	Adir	Nouveaux amides alkyl heterocycliques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent.
WO1997048694A1 (en) *	1996-06-20	1997-12-24	Board Of Regents, The University Of Texas System	Compounds and methods for providing pharmacologically active preparations and uses thereof
GB0002033D0 (en) *	2000-01-28	2000-03-22	Zeneca Ltd	Chemical compounds
GB0002031D0 (en) *	2000-01-28	2000-03-22	Zeneca Ltd	Chemical compounds
US7338956B2 (en) *	2002-08-07	2008-03-04	Sanofi-Aventis Deutschland Gmbh	Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals
CN102391207B (zh) *	2011-07-26	2014-04-09	贵州大学	N-(2-(取代苯并噻唑-2-氨基甲酰基)-苯基)-苯甲酰胺及其制备方法和用途
WO2013138753A1 (en) *	2012-03-16	2013-09-19	Fox Chase Chemical Diversity Center, Inc.	Prodrugs of riluzole and their method of use
WO2022063153A1 (en)	2020-09-24	2022-03-31	Shanghai Yao Yuan Biotechnology Co., Ltd.	Benzothiazole and quinoline derivatives and their use

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH230416A (de) *	1941-02-06	1943-12-31	Chem Ind Basel	Verfahren zur Herstellung eines neuen Kondensationsproduktes.
US3555157A (en) *	1966-08-31	1971-01-12	Tenneco Chem	Methods of protecting plants from fungi
JPS53124265A (en) *	1977-04-06	1978-10-30	Nippon Tokushu Noyaku Seizo Kk	Urea or thiourea type compounds, their preparation and insecticides contaning the same as active agent
JPS57183764A (en) *	1981-04-06	1982-11-12	Nippon Tokushu Noyaku Seizo Kk	Substituted acetanilide compound, its preparation, and herbicide

1985
- 1985-03-30 JP JP60065018A patent/JPS61225168A/ja active Pending
1986
- 1986-03-18 PH PH33545A patent/PH21114A/en unknown
- 1986-03-18 EP EP86103686A patent/EP0196547A1/de not_active Withdrawn
- 1986-03-25 US US06/843,888 patent/US4675331A/en not_active Expired - Fee Related
- 1986-03-26 DK DK143186A patent/DK143186A/da not_active Application Discontinuation
- 1986-03-26 BR BR8601372A patent/BR8601372A/pt unknown
- 1986-03-26 ES ES553447A patent/ES8706137A1/es not_active Expired
- 1986-03-27 IL IL78282A patent/IL78282A0/xx unknown
- 1986-03-27 AU AU55331/86A patent/AU5533186A/en not_active Abandoned
- 1986-03-27 DD DD86288443A patent/DD244058A5/de unknown
- 1986-03-27 ZA ZA862323A patent/ZA862323B/xx unknown
- 1986-03-28 CN CN198686102102A patent/CN86102102A/zh active Pending
- 1986-03-28 GR GR860826A patent/GR860826B/el unknown
- 1986-03-28 HU HU861320A patent/HUT41229A/hu unknown
- 1986-03-29 KR KR1019860002378A patent/KR860007231A/ko not_active Withdrawn

Also Published As

Publication number	Publication date
BR8601372A (pt)	1986-12-02
CN86102102A (zh)	1987-01-07
IL78282A0 (en)	1986-07-31
DK143186D0 (da)	1986-03-26
JPS61225168A (ja)	1986-10-06
DK143186A (da)	1986-10-01
AU5533186A (en)	1986-10-02
ZA862323B (en)	1986-11-26
PH21114A (en)	1987-07-16
EP0196547A1 (de)	1986-10-08
GR860826B (en)	1986-07-25
KR860007231A (ko)	1986-10-10
US4675331A (en)	1987-06-23
ES8706137A1 (es)	1987-06-01
HUT41229A (en)	1987-04-28
ES553447A0 (es)	1987-06-01

Publication	Publication Date	Title
EP0334135A2 (de)	1989-09-27	Trisubstituierte 1,3,5-Triazin-2,4,6-trione
EP0196547A1 (de)	1986-10-08	Neue Benzamide
EP0009762A1 (de)	1980-04-16	Substituierte N-Benzoyl-N'-tert.-alkoxycarbonylphenyl-(thio)harnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
DD159693A5 (de)	1983-03-30	Schaedlingsbekaempfungsmittel
DE1955750A1 (de)	1971-05-13	Ureidophenylguanidine,Verfahren zu ihrer Herstellung und ihre fungizide Verwendung
DD204606A5 (de)	1983-12-07	Fungizide mittel
DE2543888C3 (de)	1978-12-14	l-Phenyl-S-alkyl-S-benzylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
EP0177740A1 (de)	1986-04-16	Acylierte Saccharin-Derivate
DD248276A5 (de)	1987-08-05	Pestizides mittel
DE2813826A1 (de)	1978-10-19	Neue, substituierte (thio)-harnstoffe, verfahren zu ihrer herstellung und ihre verwendung als arthropozide, insbesondere als insektizide
EP0123861B1 (de)	1988-04-20	Harnstoffderivate
EP0113028B1 (de)	1986-04-30	Substituierte Benzylcycloalkenylharnstoff-Derivate
EP0093908A1 (de)	1983-11-16	Heteroarylthiovinyl-Verbindungen, ein Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0154273B1 (de)	1989-09-13	Fungizide Mittel
EP0318782B1 (de)	1993-01-20	Substituierte Benzoyl(thio)harnstoffe
EP0223141A1 (de)	1987-05-27	Neue Benzimidate
EP0143302A2 (de)	1985-06-05	Neue Benzoylharnstoff-Derivate und Zwischenprodukte
EP0261459A2 (de)	1988-03-30	Neue N-Benzothiazolylamide
EP0205076A1 (de)	1986-12-17	Benzaldoxim-carbamat-Derivate
EP0254150A1 (de)	1988-01-27	Decahydronapht-2-yl-alkylamine
EP0122553A1 (de)	1984-10-24	N-Sulfenylierte Phenethylsulfonamide
DD247599A5 (de)	1987-07-15	Insektizide mittel
DE3638631A1 (de)	1988-05-26	Pyrazoline, ihre herstellung und ihre verwendung als mittel mit insektizider und akarizider wirkung
DE2225873A1 (de)	1973-12-13	Isocyandiphenylaether
DE3728277A1 (de)	1989-03-09	N,n'-diacylaminale