Details
Stereochemistry | RACEMIC |
Molecular Formula | C15H15F3N2O2 |
Molecular Weight | 312.287 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C(O)(C1=CC=C(OC(F)(F)F)C=C1)C2=CN=CN=C2
InChI
InChIKey=VEVZCONIUDBCDC-UHFFFAOYSA-N
InChI=1S/C15H15F3N2O2/c1-10(2)14(21,12-7-19-9-20-8-12)11-3-5-13(6-4-11)22-15(16,17)18/h3-10,21H,1-2H3
Molecular Formula | C15H15F3N2O2 |
Molecular Weight | 312.287 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
In vitro bulb development in shallot (Allium cepa L. Aggregatum Group): effects of anti-gibberellins, sucrose and light. | 2002 Apr |
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Gibberellin inhibitors improve embryogenic tissue initiation in conifers. | 2005 Feb |
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Exogenous and endogenous growth regulators on apogamy in Dryopteris affinis (Lowe) Fraser-Jenkins sp. affinis. | 2006 Mar |
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Synergism between demethylation inhibitor fungicides or gibberellin inhibitor plant growth regulators and bifenthrin in a pyrethroid-resistant population of Listronotus maculicollis (Coleoptera: Curculionidae). | 2010 Oct |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:03:14 GMT 2023
by
admin
on
Sat Dec 16 08:03:14 GMT 2023
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Record UNII |
39B8QWM1Y2
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Record Status |
Validated (UNII)
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Record Version |
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-
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56425-91-3
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73668
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DTXSID3024108
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39B8QWM1Y2
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m5504
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admin on Sat Dec 16 08:03:14 GMT 2023 , Edited by admin on Sat Dec 16 08:03:14 GMT 2023
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flurprimidol
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admin on Sat Dec 16 08:03:14 GMT 2023 , Edited by admin on Sat Dec 16 08:03:14 GMT 2023
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