CS217403B1 - Composition against phytopathogeneous bacteria - Google Patents
Composition against phytopathogeneous bacteria Download PDFInfo
- Publication number
- CS217403B1 CS217403B1 CS808278A CS808278A CS217403B1 CS 217403 B1 CS217403 B1 CS 217403B1 CS 808278 A CS808278 A CS 808278A CS 808278 A CS808278 A CS 808278A CS 217403 B1 CS217403 B1 CS 217403B1
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- fungicide
- composition
- group
- composition according
- οληητ
- Prior art date
Links
- 241000894006 Bacteria Species 0.000 title claims description 3
- 239000000417 fungicide Substances 0.000 claims description 6
- 230000000855 fungicidal effect Effects 0.000 claims description 4
- 241000233866 Fungi Species 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 2
- 239000004094 surface-active agent Substances 0.000 claims 2
- 239000013543 active substance Substances 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 229940058303 antinematodal benzimidazole derivative Drugs 0.000 claims 1
- -1 aromatic carboxylic acids Chemical class 0.000 claims 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000012990 dithiocarbamate Substances 0.000 claims 1
- 150000004659 dithiocarbamates Chemical class 0.000 claims 1
- 239000000945 filler Substances 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical class C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims 1
- 230000003032 phytopathogenic effect Effects 0.000 claims 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 claims 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- ABEXEQSGABRUHS-UHFFFAOYSA-N 16-methylheptadecyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC(C)C ABEXEQSGABRUHS-UHFFFAOYSA-N 0.000 description 1
- CFCZCBYNIHYCRK-UHFFFAOYSA-N 2,7,7-trimethylbicyclo[3.1.1]hepta-1,3,5-triene Chemical compound CC1=CC=C2C(C)(C)C1=C2 CFCZCBYNIHYCRK-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
- 101100029848 Arabidopsis thaliana PIP1-2 gene Proteins 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- 241000223218 Fusarium Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 241000764238 Isis Species 0.000 description 1
- 101100237844 Mus musculus Mmp19 gene Proteins 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- 101100118099 Oscheius tipulae eft-2 gene Proteins 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- DBIMSKIDWWYXJV-UHFFFAOYSA-L [dibutyl(trifluoromethylsulfonyloxy)stannyl] trifluoromethanesulfonate Chemical compound CCCC[Sn](CCCC)(OS(=O)(=O)C(F)(F)F)OS(=O)(=O)C(F)(F)F DBIMSKIDWWYXJV-UHFFFAOYSA-L 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000005417 image-selected in vivo spectroscopy Methods 0.000 description 1
- 238000012739 integrated shape imaging system Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/13—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
- C07C205/26—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups and being further substituted by halogen atoms
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
- A01N33/18—Nitro compounds
- A01N33/20—Nitro compounds containing oxygen or sulfur attached to the carbon skeleton containing the nitro group
-
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/13—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
- C07C205/14—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to acyclic carbon atoms
- C07C205/15—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to acyclic carbon atoms of a saturated carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Air Conditioning Control Device (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
- 1 - 217 403
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Taxon ©Čpaeon, ycTpaaawpca caeaywie TexHXxecxxe χβΛοοτβτχχyxe ΗβΒβοτΗΗΧ pemeaxft: 217 403 1. 3HawMTejibHO MCKxrowaxxrcfl τοκομπηηθ αία pacTeHHft κ τθπλο-ΚΡΟΒΗΗΧ ΧΜΒΟΤΗΗΧ ΠΟδΟΆΗΗβ ΑβδοΤΒΗΗ, 8 ΤβΚΧβ ΓγΜΘΗΜβΛΜΙίΚΗΟΚΜβOnaceHMH, C ΚΟΤΟρΗΜΗ £0 CMX πορ ΑΟΛΧΗΗ δΗΛΜ ΜΙφΚΤΒΟΛ
2. ΠγΤβΜ ΚΟΜόΗΗβΙξΗΜ βθΚΤβρΜΠΜΑΗΗΧ Μ φ^ΓΗΓΜρΜΑΗΗΧ fleftCTByBIUHXBemecTB c paa^w^HHMM cbo$ctb8MM woryp ÓHTb ycTaHOBxeHH οτβ-neHb fleftCTBHfl Μ οπβκτρ fleiiCTBMfl npenapaTOB B COOTBeTCTBKH C peJIbX) ΠρίίΜΘΗΘΗΜΗ 3. Η3-3Θ KOMČHHIípOBaHHOrO ΙφΟΜβΗΘΜΗ paajIÍÍHHHX £eft CTByXXQKXBenjecTB no^yuaeTCH βηοοκθη hbpojího—χοβπίίοτΒθΗΗθΗ βηγοαθ. B xa^iecTBe ι^ηγηφιληογο napTHepa aha κοΜδκΗβΐξκίϊ, corxacHO8TOMy ΜΒΟόρβΤβΗΜΚ), ΑΒΛΗΒΤΟΗ ΠρΜΓΟΑΗΗΜΜ Μ3Ββ<3ΤΗΗβ (fjyHmitH^Uj KOTOpne ΜΜβϊΟΤ ΟΤ^θΤΛΜΒΟθ MJIM ΒΗρθΧβΗΗΟβ ,ΖξβδΟΤΒΜβ ΠρΟΤΜΒ/Basidiomyceten, Phycomyceten, Asmomyceten, Fungi imperfekt!,/
OcoCeHHO AHA 3Τ0Γ0 npMrOflHH (^/ΗΓΪίΠΗ,ΖξΗ M3 KJiaCCa COeflHHMeHMÍideHSMMHaaSOJIOB KWH 0eH3MMH,Zj;a3OJIOOĎpa8yCTHttX, φΤΘΛΜΜΜΛΟΒ, flMTM-OKapčaMaTOB κ 8Ημλμ,π;οβ raTepopHKjinqecKJix n apoMaTMtiecKKXKapČoHOBux kkcaot. B xa^ecTBe npnwepoB rasi npMBe^eHHux oaccoBcoeAMHeHiiii moscho paccMaTpHBaTb m b KatíecTBe bboahmhx neftcT-ByxmiKX semecTB μλμ mx κομΟμηθαμμ Apyr c npyroM, corxacHOΜ3θ6ρθτθΗκκ>, moscho πρΜΜβΗΗΤΒ cAeAywie ^eitcTByraiMe BemeeTsa: 1 — ( - óyTMJtKapSaMOíuC - 2 - (MeTOKCM-KapČOKcaMHflo) - δβΗ3ΚΜΗ£θ3ΟΛ 2 - (Μβτοκοκ-KapóoKcaMMAo) - 6βΗ3ΗΜΚ,ζξθ30Λ 1,1 -0-φβΗΗΛ-0ΗΟ-(3,3-ΘΤΟΚΟΜΚθρδθΗΗΛ-ΤΜΟΜΟ*ΙβΒΗΗθ) 1,1 —O—φβΗΚΛ—ÓKC—(3,3 -ΜβΤΟΚΟΜΚβρδΟΗΚΛ-ΤΚΟΜΟΠβΒΜΗθ) 2 - (4-ΤΜΘβΟΛΚΛ) -6θΗ3ΗΜΜΑβ8ΟΛ 2 - (2^ypMJI ϊ-δβΗ3ΜΜΗΑβ30Λ -ΤρΗΧΛΟρΜβΤΜΛΤΜΟ-ΤβΤρθΓΜΑφΤβΛΗΜΗΑ-TPHXJÍ ΟΜβΤΗΛΤΗΟ-φΤ βΛΜΜΜΛ -(1,1,2,2-ΤβΤρβΧΛ0ρ3ΤΜΛΤΗ0)-ΤβτρβΓΗΛρΟφΤΘΛΚΜΚΑ ΘΗΚΛΚΗ-Ο -ίίθΛ6θΗ3θβΗθϋ ΚΗΟΛΟΤΗ βΗΗΛΜΑ-2,3-ΖξΗΓΚ£ρθ-6-ΜβΤΗΛ-1,4-0Κ0βΗ«ΗΗ-5-Κβρδ0Η0Β0ϋ ΚΚΟΛΟΤΗ2,3-ΑΗΓΜΛΡ0-6-ΜβΤΗΛ-1,4-0KC8TKKH-5-ΚβρδΟΗΟΒβΗ KKCXOTa-
βΗΚΛΜΑ- , -AHOKCMA ΘΗΜΛΚ,Ζξ—2“ΜΘΤΜΛ—0βΗ SOÍÍHOK Κ Μ ΟΛΟ ΤΗ 217 403
aHHJiMfl-2,5-flMMeTKJi$ypaH-3 KapCoHOBoK khcjiothβΗΜΛΜΛ-2-ΜβΤ1ϋΙ-5,6-ΛΜΓΜΛρ0-4-4-ΠΜρβΗ-3-Κβρδ0Η0Β0ϋ KHCJIOTH
UHHK-9TMJieH-l, S-ÓKC-flMTKOKapČSMaT ΤβΤρθΜβΤΜΛΤΜ3ΓρβΜΛΜ0γΛΒφΜΛ Μ ΘΗ ΓβΗβ P“ STHJie Η-1,2-<5 HC-flMTHO Κ βρ 6 GU βΤ 3,5--ΛΜΜβΤΜΛ-ΤβΤρθΓΜΛρθ-1,3,5-ΤΗ84ξΖβ3ΜΗ-ΤΗΟΗ ( 2 ) ΙίΜΗΚ-ΠρΟΠΜΛβΗ-δΜΟ-ΛΜΤΗΟΚβρδθΜΘΤ ΒβκρβτζρκΑΗΟ fle®CTByraiMe πβρτΗβρΗ κοΜδΗΗβςΗβ οδπξβϋ $opMyjiH1 WaCTMHHO ΗΟΒΜβ Η ΜΟΓΜΤ 6íJTb Κ3ΓΟΤΟΒΛβΗΗ ΠΟ HSBeCTHHM Η3jiMTepaTypu cnocoČaM (HanpHMep, Ber. dtsch. Chem. Ges. 52, 395/ISIS/; Rocznicki Chem. 26,571 /1952/; J. org.Chem. 8,1 /1943/ J. Chem. Soc. /London/ 1S47, 1518;
BamiaAHoe οπμοθηηθ μ3ο6ρθτθημπ k HeaKpenTOBaHHofó saaBKe ΦΡΓ1 768 9®6, ΒΗΚΛβΛΗΟβ onMcaHue αβοδρβτβΗΗΗ κ ΗββκΐίβπτοΒβΗΗοδsaHBKe ΦΡΓ 1 804 068, βηκλθληο6 onncaHMe HsoCpeTeHHH κ HeaK-ςβπτοΒβΗΗοϋ saflBKe ΦΡΓ 1 954 173 m samia^Hoe απκοβΗΜβ m3o6-ρβτβΗΗΗ κ ΗββκηβπτοΒβΗΗοϋ eaaBKe ΦΡΓ 1 768 778). B KawecTBe Φυηγμρηληο .neitcTByromHx κομποηθητοβ cjiyacaT οτβΗ#&ρτηηθ Ae&CTByxxqiie BeiqecTBa.
CoraacHO Μ300ρβτβΗΗχ>, sahana peniaeTca τβΜ, hto c noMoiqtroΤΒβρΛΗΧ h/hJIH JKHflKMX ΗβΠΟΛΗΗΤβΛβϊί <$OpMyjIHpy»T ΠρβΠβρβΤΗ,κοτορκβ coflepxaT b οδιςβΜ 0,1 - 2% CaKTepMUMflHHX « 20-80%$yHrimMflHOEO (hx) neíicTBynmero (wx) BemecTBa (b(.
ΠΡΚΜΕΡΗ OCymECTBJIEHMH
1. Ms SToro npiiMepa ΒΗτβκββτ xopomee ČaKTepHiíH^Hoe h $yHru-pMflHoe .seíicTBHe Ηβκοτορκχ npenapaTOB. προΒβΛβΗΗΗ οπητθγομογθηηο BMemanw ^eíícTByícqMe seiqecTBa b KOHpeHTpau,ww 0,5%b nnnaTejibHy» cpe^y c arapoM η προηββθλη MHOKyjtamin cTepnjib-HO# arapOBOS nJiaCTHHKH paSJIWHHiíMW δβΚΤβρΗΗΜΗ H rpiíSaMM b pas-JIHHHHX CMCTeMaTMneCKWX ΠΟΛΟΚβΗΜΗΧ. ΠοΟΛβ COOTBeTCTBysameííKHKyóauwH b τβρΜοοτβτβ βηηβηλοοβ δβκτβρΜοοτβτΗΗβοκκβ h $yHrrMflTaTKqecKue ΛβϋοτΒΗΗ. PesynbTaTH ΗβκοτορΗχ OTÓpaHHHX οπη-TOB npeACTaBJíeHU B ΤβόΛΖρβ 1. ΠρΗΜβΗΗβΜΗβ B ΤθδΛΜρβΧ 1 H 2CMMBOJIH ΜΜβΐΟΤ CJieflyKUIJMe 3ΗβΗΘΗΜΗ J 217 403 JEftCTBymMB ΒΕΰΕΒΟΤΒΑ A 1 - 6pOM—ÍHMTpO«“3f3|3-·τρΐΙΧΛ0ρ···Πρ0ΠβΗ0Λ (2) B 2-6pOM-2HKTpo-STaHOJt B ΧΛΟρβΜφθΗΜΚΟΛ F 2-ΗΪΪΤρθ-113-ΛΗΠΜΠβρΗΛΜΗ0-Πρ0ΠβΗ JI 2-6pOM-2-HMTpO-l ,3-ČKC (φθΗΗΛΚθρ6θΜ0ΜΛ0Κ0Μ)--Πρ0ΠβΗE 2-6ρ0Μ-2-ΗΗΤρ0-Πρ0ΠβΗΛΜ0Λ-(1,3) X 2-(MeTOKcn-Kap6oKcaMM(no)-CeH8MMH1naa<XH3 Η-ΤρΜΧΛΟρΜΘΤΜΛΤΚΟ-ΤβΤρθΓΜΑρΟφΤ aZHMHAΜ ΤβΤρβΜΖΤΐυΐγρ8ΜΛΜ0γΛϊ>φΜΑ K 2,3-ΛΜΓΗΛΡ0-6-ΜΘΤΐυΐ-1,4-OKCaTHÍlH-5-Kap6OHOBaH ΚΗΟΛΟΤΘ-ΘΗΜΛΜΛ Jí ΠΚΗΧ~8·ΡΗΛΘΗ-1,2-βΗ0~ΑΗΤΗ0Κ8ρ6βΜαΑβΤ Μ 2-(4-ΤΜβ8ΟΛΗΛ)*0βΗ8ΗΜκΛβ8ΟΛ OUEHKA JEftCTBHfl +++ ΠΟΛΗΟβ ΤΟρίΙΟΧβΗΚβ ρΟΟΤΘ
++ ΟΗΛΒΗΟβ ΤΟρΜΟΜβΗΜβ pOCTS + Majioe τορΜοχβΗΜβ pocTa
o He fleftcTByeT - He npoBepexocb 2. ŤopMyjmpoBKa nopoinxa λλλ οπρηοκηβθημθ 60% φγΗΓΗΐίΐνξΗΟΓο (hx) AeftcTBynnero (mx) ÓemecTBa (b)0,4% OaKTepHUMAHoro neftcTBynnero BeqecTsa (b) 20,6% xaozHHa
10% βΜΟρφΒΟΑ ΚρβΜΗβΒΟϋ KKCZOTH 5% noponuca oOapaĎGTaHHoro cyzs^HTHoro mezoxa 4% ΘΛΚΜΖΒΟγΖΗφΟΗβΤβ
Κομποηθhtn nepeMdmxBazK κ b saKznnexxx tohko paeuaxKBaffK 3. BopbCa c CaxTepxaabHHMH BzaxHHMH rxxzxiix xzy6xeft x rpxfiKOBNMM CyXKMX ΓΗΚΛΧΜΚ ΠβρβΑ ΟΚΖΒΑΧρΟΒΘΧΧΘΜ· 217 403 ΚκγβΗΜ «enocpe.ncTBeHHo nocjie cCopa ypoxaji οΰρβόβτκΒβΛΗ on-pHCKXBaHHeií CpaflCTBOM, COTJiaCHO ΜΒΟΟρβΤβΗΗΒ. JUfl 3Τ0Γ0 200 Γcpe^CTBa cycneH^xpoBaaM b 300 μλ βολή μ ηηηοομλη Ha 100 κγK^yĎHeS.
KayÓHH coxpaHií.«HCJi λο βθοηη. Η KOHi^y nepHO^a χρθηθηηη onpe-ΛΘΛΜΛΗ ΛΟΛΒ ΓΗ1ΚΛΗ ΠρΗ ΧρβΗΘΗΗΜ.
PeeyjibTaTH οπητοβ πρκΒβΛβΗΗ χ τββΛΜίχβ 2. 217 403
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TaCjiwga 2 217 403
CpegCTB©__Macca imyCHeft b %_
SgOpOBUe ΒΛΘΧΗΝβ ΓΗΜΛΗβ CyXUe ΟΜβΠΙβΚΗΙΙβ ΓΗΗΛΙΙβ ΓΗκΛΝβ
HeoĎpaÓo- 20 9 ? 64 ΤΘΗΗΗβ ® ♦ C 56 1 3 40 3 + B 82 2 4 12 S+M+K+E 91 2 2 5 JI + K + A 80 1 3 16 Μ + K + B 89 1 4 6 JI 22 16 2 60 A 25 4 6 65 - η - 217 403
ΦΟΡΜΥΤΙΑ H30BPETEHKH 1. Cpe^cΤΒΟ ΜΛ ĎOpbĎH C φΜΤΟΠβΤΟΓβΗΗΗΜΜ 6βΚΤβρίΟΙΙΜ Μ rpHČ-Κ8ΜΜ β pacreHKeBOflCTBe κ β cexbCKOM xosaftcTBe, oTXMHaraqeecHCOAepXaHHeM ΗΗΤρΟβΛΚβΗΟΛΟΒ φΟρίίγΛΗ 1. tf ί* g C CH OH 1 ΓΛβ £ ΒΟΛΟρΟΛ ΗΧΗ ΓΗΛΡΟΚΟΒΒΛΚΚΛ U* BOflOpOfl, ΧΛΟρ, ĎpOM HXM ΓΗΛρΟΧΟΒβΧΚΜΛ Μ ΒΟΛ©Ρ©Λ, βΛΚΗΛ ΗΧΗ τρΗΧΧΟρΜβΤΗΧ Η ΗβΒΘΟΤΗΗΧ φγΗΓΜηΚ^ΟΒ,Η Spilky C ΗβΠΟΛΗΗΤβΛΗΜΗ, m/iíUIH ρββδβΒΚΤβΧΗΜΗ, μ/5ΙΧΗ ΠΘΒβρΧ-ΗΟΟΤΗΟ-βΚΤΗΒΗΗΜΚ ΟρβΛΟΤΒβΜΒ ΗΛΗ ΒβΠξΒΟΤΒΘΜΗ, ΚΟΤΟρϋβ ΟΠΟΟΟδ-CTByKT CnOCOČHOCTK ΠρΟΗΜΚΟΒΜΗ XeftCTByiXqHX BenjeCTB. 2. ΦγΗΓκςΗΑ, corxacHO nyHKTy 1, OTXíroawrites τθμ, hto obothocktch κ xxaccy coeflHHeHH$ ÓeHSHMHxaeoxoB. 3. ΦγΗΓΒΐχκ,α;, corxacHO nyHKTy 1, QTxvnansnp&ca τθμ, hto obothocíitck x xxaccy coeAHBeHHft φτβχιηΐΗΛΟΒ. 4. Φ^ΓΜΙξΒΛ, ΟΟΓΧβΟΗΟ nyHKTy 1, OTXBHaHUMfiCH ΤβΜ, BTO OHOTHOCHTCH K Kjiaccy ΟΟβΛΜΗβΗΜβ ΗΗΗΧΗχΟΒ ΓβΤβρΟηΜΚΧΗΒβΟΧΚΧ ΗapoMaTHuecKHX xapĎoHOBux xmcxot. 5. 'JyHrHnHfl, corxacHO nyHKTy 1, OTJiwqaKmJíftcH τβ«, hto ohOTHOCHTCH K Kaaccy ΟΟβχΜΗΘΗΚΚ χΗΤΗΟΚβρδθΜΘΤΟΒ. 6. Φ^ΓΜηκη, corxacHO nyHKTy 1, OTXHHaranHScH τβΜ, hto ohcoctohit ne KOMČHHanHii $yHrMnHAOB, corxacHO nyHKTHM 2-5, 12
AHHOTAW 217 403 ΗβΟδρβΤβΗΜβ KaeaeTCfl δβΚΤβρΜίρίΛΗΗΧ CpeflCTB flJIH ÓOpbÓH c φκτο-ΠβΤΟΓΘΗΗΗΜΜ ÓβΚΤβρΚΗΜΗ íl rpHÓSUM Β CeJIbCKOM XOBaftCTBe M CSflO-βοαοτβθ. Cpeflcrua coaepxaT κ KanecTBe fleficTByíomiíx semecTB CMecbφγΗΓΜΙξΖΛΟΒ W3 KJiaCCOB 6βΗ8ΜΜΜΛΘ3ΟΛΟΒ ΗΛΗ 6βΗ3ΗΜΪΙΛΘ8ΟΛ-θ6ρβ3γΚ>-iqkx, φτβΛβΜΗΛΟβ, aHaxHAOB reTepomncjureecKHX h apoMaTHwecKHxKapCOHOBHX KHC.aOT MJIM ΛΜΤΗΟΚβρόΟΜΘΤΟΒ H ĎaKTepMl^MflOB M8 KJiaC-ca coeflHHeHiiíi ΗΗτροβΛκβΗοχοΒ oCmeft φορΜγΛΝ
R C CH
OH
ΓΛβ cooTBercTByeT eo^opofly μλμ rKflpoKCíiaaKiuy, cooTBeTCTByeT sonopofly, xjiopy, CpoMy on niapoKCMaaK&ay κcooTBeTCTByeT Bonopony, ajiKiwy hjim TpHxaopMeTHxy. ΠβοδρβτθΗΗβ npecxenyeT uexb npefloapaTHTb ΜζκροόΗΝβ aaĎojieBa-hmh KyabTypHHx pacTeHuft bo spěni ΒβΓβτβΐίΚΟΚΗΟΓΟ nepMo.ua mMKKpoĎHo-oCycjioBjíeHHHe ηοτβρΜ bo apeira xpaHeexa nponyicroBypozaa Ha cKzanax·
Claims (5)
- - 13 - 217 403 PŘEDMĚT VYNÁLEZU1. Prostředek proti fytopatogenním bakteriím a houbám připěstování rostlin a v zemědělství, vyznačující se tím,že obsahuje nitroalkanoly obecného vzorce I R' R" I' I R - c - CH - OH (I), I no2 kde R znamená vodík nebo hydroxyalkyl, R' znamená vodík, chlor, brom nebo hydroxyalkyl aR "znamená vodík, alkyl nebo trichlormethyl a známé fungicidy spolu s plnivy a/nebo ředidly a/nebopovrchově aktivními látkami nebo látkami způsobujícímipronikání účinných látek.
- 2. Prostředek podle bodu 1, vyznačující se tím, že fun-gicid je vybrán ze skupiny benzimidazolových derivátů. Prostředek podlecid je vybrán ze bodu 1, vyznačující se tím,že fungi-skupiny ftalimidových derivátů.
- 4. Prostředek podle bodu 1, vyznačující se tím,že fungi-cid je vybrán ze skupiny anilidů heterocyklických aaromatických karboxylových kyselin.
- 5. Prostředek podle bodu 1,vyznačující se tím,že fungicidje vybrán ze skupiny dithiokarbamátů.
- 6. Prostředek podle bodu 1, vyznačující se tím,že fungi-cid je vybrán ze z kombinací fungicidů podle bodů 2 až 5 · Uznáno vynálezem na základě výsledků expertizy,provedenéÚřadem pro vynálezectví a patentnictví, Berlín, (DD)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
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| DD20308878A DD133885B1 (de) | 1978-01-04 | 1978-01-04 | Mittel zur bekaempfung von phytopathogenen bakterien und pilzen |
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| Publication Number | Publication Date |
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| CS217403B1 true CS217403B1 (en) | 1983-01-28 |
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| CS808278A CS217403B1 (en) | 1978-01-04 | 1978-12-06 | Composition against phytopathogeneous bacteria |
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| CS (1) | CS217403B1 (cs) |
| DD (1) | DD133885B1 (cs) |
| DE (1) | DE2853040A1 (cs) |
| FR (1) | FR2413879A1 (cs) |
| GB (1) | GB2016273B (cs) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| EP0231488A1 (de) * | 1985-12-23 | 1987-08-12 | Bayer Ag | Mittel zur Beizung von Pflanzkartoffeln |
| DE3622976A1 (de) * | 1986-07-09 | 1988-01-21 | Bayer Ag | Fluor enthaltende dimethylolnitromethane, verfahren zu ihrer herstellung sowie ihre verwendung |
| EP0291561A1 (de) * | 1987-05-19 | 1988-11-23 | Bayer Ag | Mittel zur Beizung von Kartoffeln, die für Ernährungszwecke bestimmt sind |
| GB8830266D0 (en) * | 1988-12-24 | 1989-02-22 | Laporte Industries Ltd | Absorbent material |
| JP5645840B2 (ja) | 2008-12-02 | 2014-12-24 | 株式会社Wave Life Sciences Japan | リン原子修飾核酸の合成方法 |
| IN2012DN00720A (cs) | 2009-07-06 | 2015-06-19 | Ontorii Inc | |
| JP5878758B2 (ja) * | 2009-09-16 | 2016-03-08 | 株式会社Wave Life Sciences Japan | Rna及びその誘導体合成のための新規保護基 |
| US10428019B2 (en) | 2010-09-24 | 2019-10-01 | Wave Life Sciences Ltd. | Chiral auxiliaries |
| RU2014105311A (ru) | 2011-07-19 | 2015-08-27 | Уэйв Лайф Сайенсес Пте. Лтд. | Способы синтеза функционализованных нуклеиновых кислот |
| SG11201500232UA (en) | 2012-07-13 | 2015-04-29 | Wave Life Sciences Pte Ltd | Chiral control |
| CA2879066C (en) | 2012-07-13 | 2019-08-13 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant |
| SG11201500239VA (en) | 2012-07-13 | 2015-03-30 | Wave Life Sciences Japan | Asymmetric auxiliary group |
| WO2015108046A1 (ja) | 2014-01-15 | 2015-07-23 | 株式会社新日本科学 | 抗アレルギー作用を有するキラル核酸アジュバンド及び抗アレルギー剤 |
| JPWO2015108047A1 (ja) | 2014-01-15 | 2017-03-23 | 株式会社新日本科学 | 免疫誘導活性を有するキラル核酸アジュバンド及び免疫誘導活性剤 |
| US10149905B2 (en) | 2014-01-15 | 2018-12-11 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant having antitumor effect and antitumor agent |
| KR102423317B1 (ko) | 2014-01-16 | 2022-07-22 | 웨이브 라이프 사이언시스 리미티드 | 키랄 디자인 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR922380A (fr) * | 1945-02-15 | 1947-06-06 | Geigy Ag J R | Produits antiparasitaires |
| US3415936A (en) * | 1963-11-26 | 1968-12-10 | Phillips Petroleum Co | Bactericide for brine injection |
| GB1145496A (en) * | 1965-06-29 | 1969-03-12 | Thomson Res Associates Ltd | Control of fungal disease in trees |
| GB1193954A (en) * | 1966-08-12 | 1970-06-03 | Boots Pure Drug Co Ltd | Control of Micro-Organisms |
| US3546346A (en) * | 1969-03-24 | 1970-12-08 | Morton Int Inc | Systemic plant and seed fungicide comprising 1,1,1 - trichloro - 2 - hydroxy-3-nitropropane |
| DE2054887A1 (en) * | 1970-11-07 | 1972-05-10 | Badische Anilin- & Soda-Fabrik Ag, 6700 Ludwigshafen | Antifungal bromonitroalkanols - for plant protection |
-
1978
- 1978-01-04 DD DD20308878A patent/DD133885B1/de not_active IP Right Cessation
- 1978-12-06 CS CS808278A patent/CS217403B1/cs unknown
- 1978-12-08 DE DE19782853040 patent/DE2853040A1/de not_active Ceased
-
1979
- 1979-01-03 GB GB7900125A patent/GB2016273B/en not_active Expired
- 1979-01-03 FR FR7900072A patent/FR2413879A1/fr active Pending
- 1979-01-04 NL NL7900046A patent/NL7900046A/xx not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| GB2016273B (en) | 1982-06-30 |
| NL7900046A (nl) | 1979-07-06 |
| GB2016273A (en) | 1979-09-26 |
| FR2413879A1 (fr) | 1979-08-03 |
| DD133885B1 (de) | 1981-02-25 |
| DD133885A1 (de) | 1979-01-31 |
| DE2853040A1 (de) | 1979-07-12 |
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