JPS597105A

JPS597105A - 農園芸用殺菌剤

農園芸用殺菌剤

Info

Publication number: JPS597105A
Authority: JP; Japan
Prior art keywords: compound; agricultural; diseases; sprayed; control
Prior art date: 1982-07-03
Legal status : Granted

Application number

JP57114795A

Other languages

English (en)

Japanese (ja)

Other versions

JPH023764B2 (enrdf_load_stackoverflow

Inventor

Takuo Wada

和田　拓雄

Katsumi Sato

克己佐藤

Current Assignee

Hokko Chemical Industry Co Ltd

Original Assignee

Hokko Chemical Industry Co Ltd

Priority date

1982-07-03

Filing date

1982-07-03

Publication date

1984-01-14

1982-07-03 Application filed by Hokko Chemical Industry Co Ltd filed Critical Hokko Chemical Industry Co Ltd

1982-07-03 Priority to JP57114795A priority Critical patent/JPS597105A/ja

1984-01-14 Publication of JPS597105A publication Critical patent/JPS597105A/ja

1990-01-24 Publication of JPH023764B2 publication Critical patent/JPH023764B2/ja

Status Granted legal-status Critical Current

Links

230000002070 germicidal effect Effects 0.000 title abstract 3
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125000000217 alkyl group Chemical group 0.000 claims abstract description 3
239000000417 fungicide Substances 0.000 claims description 11
239000004480 active ingredient Substances 0.000 claims description 7
230000000855 fungicidal effect Effects 0.000 claims description 7
125000005843 halogen group Chemical group 0.000 claims description 3
WLLGXSLBOPFWQV-UHFFFAOYSA-N MGK 264 Chemical compound C1=CC2CC1C1C2C(=O)N(CC(CC)CCCC)C1=O WLLGXSLBOPFWQV-UHFFFAOYSA-N 0.000 claims 1
125000004429 atom Chemical group 0.000 claims 1
230000000694 effects Effects 0.000 abstract description 11
239000000126 substance Substances 0.000 abstract description 7
230000002195 synergetic effect Effects 0.000 abstract description 3
230000002708 enhancing effect Effects 0.000 abstract description 2
229910052736 halogen Inorganic materials 0.000 abstract 2
150000002367 halogens Chemical class 0.000 abstract 2
QXJKBPAVAHBARF-UHFFFAOYSA-N procymidone Chemical compound O=C1C2(C)CC2(C)C(=O)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-UHFFFAOYSA-N 0.000 abstract 2
230000001276 controlling effect Effects 0.000 abstract 1
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LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
201000010099 disease Diseases 0.000 description 23
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CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
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RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
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QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical group COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
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