Details
Stereochemistry | ACHIRAL |
Molecular Formula | C11H6Cl2N2 |
Molecular Weight | 237.085 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=C(Cl)C(=CC=C1)C2=CNC=C2C#N
InChI
InChIKey=FKLFBQCQQYDUAM-UHFFFAOYSA-N
InChI=1S/C11H6Cl2N2/c12-10-3-1-2-8(11(10)13)9-6-15-5-7(9)4-14/h1-3,5-6,15H
Molecular Formula | C11H6Cl2N2 |
Molecular Weight | 237.085 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
The ABC transporter BcatrB from Botrytis cinerea is a determinant of the activity of the phenylpyrrole fungicide fludioxonil. | 2001 May |
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Interactions between nematophagous fungi and consequences for their potential as biological agents for the control of potato cyst nematodes. | 2003 Jan |
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Synthesis and phloem mobility of acidic derivatives of the fungicide fenpiclonil. | 2004 Nov |
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Expanding the paradigms of plant pathogen life history and evolution of parasitic fitness beyond agricultural boundaries. | 2009 Dec |
|
Fungicide-driven evolution and molecular basis of multidrug resistance in field populations of the grey mould fungus Botrytis cinerea. | 2009 Dec |
|
Efflux in fungi: la pièce de résistance. | 2009 Jun |
|
Effects of pesticides on the bacterial production of pyrrolnitrin. | 2010 May 12 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 07:38:23 UTC 2023
by
admin
on
Sat Dec 16 07:38:23 UTC 2023
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Record UNII |
21OCB8KDQ9
|
Record Status |
Validated (UNII)
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Record Version |
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-
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fenpiclonil
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admin on Sat Dec 16 07:38:23 UTC 2023 , Edited by admin on Sat Dec 16 07:38:23 UTC 2023
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m5288
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admin on Sat Dec 16 07:38:23 UTC 2023 , Edited by admin on Sat Dec 16 07:38:23 UTC 2023
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C437165
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34759
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74738-17-3
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21OCB8KDQ9
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91724
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DTXSID0036633
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admin on Sat Dec 16 07:38:23 UTC 2023 , Edited by admin on Sat Dec 16 07:38:23 UTC 2023
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