Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H13O5.Na |
| Molecular Weight | 320.2719 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].CC(=O)CC(C1=CC=CO1)C2=C([O-])C3=C(OC2=O)C=CC=C3
InChI
InChIKey=SVFRZMWUJFQZQP-UHFFFAOYSA-M
InChI=1S/C17H14O5.Na/c1-10(18)9-12(13-7-4-8-21-13)15-16(19)11-5-2-3-6-14(11)22-17(15)20;/h2-8,12,19H,9H2,1H3;/q;+1/p-1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Analysis of multiple anticoagulant rodenticides in animal blood and liver tissue using principles of QuEChERS method. | 2010-06 |
|
| Identification and determination of coumateralyl and coumafuryl in animal tissues by high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry. | 2008-07 |
|
| Multiresidue analysis of seven anticoagulant rodenticides by high-performance liquid chromatography/electrospray/mass spectrometry. | 2007-02-07 |
Patents
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| Code System | Code | Type | Description | ||
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DTXSID4058364
Created by
admin on Mon Mar 31 21:46:01 GMT 2025 , Edited by admin on Mon Mar 31 21:46:01 GMT 2025
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U4C9YC2F9J
Created by
admin on Mon Mar 31 21:46:01 GMT 2025 , Edited by admin on Mon Mar 31 21:46:01 GMT 2025
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34490-93-2
Created by
admin on Mon Mar 31 21:46:01 GMT 2025 , Edited by admin on Mon Mar 31 21:46:01 GMT 2025
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23707507
Created by
admin on Mon Mar 31 21:46:01 GMT 2025 , Edited by admin on Mon Mar 31 21:46:01 GMT 2025
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PRIMARY |
SUBSTANCE RECORD
