PL216069B1 - Pirazolilokarboksyanilidy, sposób ich wytwarzania, srodki do zwalczania niepozadanych drobnoustrojów, sposób zwalczania niepozadanych drobnoustrojów, sposób wytwarzania srodków do zwalczania niepozadanych drobnoustrojów, hydroksyalkilopirazolilokarboksyanilidy, sposób wytwarzania hydroksyalkilopirazolilokarboksyanilidów, fluorowcopirazolilokarboksyanilidy, sposób wytwarzania fluorowcopirazolilokarboksyanilidów, ketony, sposób wytwarzania ketonów - Google Patents

Info

Publication number

PL216069B1

PL216069B1 PL365036A PL36503602A PL216069B1 PL 216069 B1 PL216069 B1 PL 216069B1 PL 365036 A PL365036 A PL 365036A PL 36503602 A PL36503602 A PL 36503602A PL 216069 B1 PL216069 B1 PL 216069B1

Authority

PL

Poland

Prior art keywords

group

formula

optionally

halogen

optionally substituted

Prior art date

2001-07-25

Links

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• 239000000417 fungicide Substances 0.000 title description 5
• 238000000034 method Methods 0.000 claims abstract description 111
• 244000005700 microbiome Species 0.000 claims abstract description 26
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• 230000008569 process Effects 0.000 claims description 71
• 150000001875 compounds Chemical class 0.000 claims description 45
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• 150000002367 halogens Chemical class 0.000 claims description 38
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• 239000002253 acid Substances 0.000 claims description 25
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• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 20
• 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 20
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• 239000003795 chemical substances by application Substances 0.000 claims description 10
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• 239000000460 chlorine Substances 0.000 claims description 9
• 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 8
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 8
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• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
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• 125000004369 butenyl group Chemical group C(=CCC)* 0.000 claims description 3
• 125000000480 butynyl group Chemical group [*]C#CC([H])([H])C([H])([H])[H] 0.000 claims description 3
• 125000003493 decenyl group Chemical group [H]C([*])=C([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
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• 230000018044 dehydration Effects 0.000 claims 1
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• 239000013543 active substance Substances 0.000 description 25
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