Details
Stereochemistry | RACEMIC |
Molecular Formula | C22H18N2O4 |
Molecular Weight | 374.3893 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(OC(=O)N(NC2=CC=CC=C2)C1=O)C3=CC=C(OC4=CC=CC=C4)C=C3
InChI
InChIKey=PCCSBWNGDMYFCW-UHFFFAOYSA-N
InChI=1S/C22H18N2O4/c1-22(16-12-14-19(15-13-16)27-18-10-6-3-7-11-18)20(25)24(21(26)28-22)23-17-8-4-2-5-9-17/h2-15,23H,1H3
Molecular Formula | C22H18N2O4 |
Molecular Weight | 374.3893 |
Charge | 0 |
Count |
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Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
PubMed
Title | Date | PubMed |
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[Determination of famoxadone residue in oranges by GC]. | 2005 May |
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Effect of mutations in the cytochrome b ef loop on the electron-transfer reactions of the Rieske iron-sulfur protein in the cytochrome bc1 complex. | 2007 Feb 20 |
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Effect of the use of recent commercial fungicides [under good and critical agricultural practices] on the aroma composition of Monastrell red wines. | 2008 Jun 9 |
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Influence of several fungicides on the antioxidant activity of red wines (var. Monastrell). | 2009 Aug |
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Generation and characterization of isolates of Peronophythora litchii resistant to carboxylic acid amide fungicides. | 2010 May |
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Environmental impact on vascular development predicted by high-throughput screening. | 2011 Nov |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:04:02 GMT 2023
by
admin
on
Sat Dec 16 09:04:02 GMT 2023
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Record UNII |
V1C07OR6II
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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EPA PESTICIDE CODE |
113202
Created by
admin on Sat Dec 16 09:04:02 GMT 2023 , Edited by admin on Sat Dec 16 09:04:02 GMT 2023
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m5242
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PRIMARY | Merck Index | ||
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213032
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Famoxadone
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famoxadone
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131807-57-3
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7266
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DTXSID8034588
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59340
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V1C07OR6II
Created by
admin on Sat Dec 16 09:04:02 GMT 2023 , Edited by admin on Sat Dec 16 09:04:02 GMT 2023
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PRIMARY |