Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H14O3 |
| Molecular Weight | 230.2592 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)C(=O)C1C(=O)C2=C(C=CC=C2)C1=O
InChI
InChIKey=RZKYEQDPDZUERB-UHFFFAOYSA-N
InChI=1S/C14H14O3/c1-14(2,3)13(17)10-11(15)8-6-4-5-7-9(8)12(10)16/h4-7,10H,1-3H3
| Molecular Formula | C14H14O3 |
| Molecular Weight | 230.2592 |
| 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 |
|---|---|---|
| Analysis of multiple anticoagulant rodenticides in animal blood and liver tissue using principles of QuEChERS method. | 2010-06 |
|
| Simultaneous measurement of indandione-type rodenticides in human serum by liquid chromatography-electrospray ionization- tandem mass spectrometry. | 2009-08-06 |
|
| Analysis of indandione anticoagulant rodenticides in animal liver by eluent generator reagent free ion chromatography coupled with electrospray mass spectrometry. | 2008-12-05 |
|
| Multiresidue analysis of seven anticoagulant rodenticides by high-performance liquid chromatography/electrospray/mass spectrometry. | 2007-02-07 |
|
| Effect of the anticoagulant, pindone, on the breeding performance and survival of merino sheep, Ovis aries. | 2005-03 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:15:48 GMT 2025
by
admin
on
Mon Mar 31 19:15:48 GMT 2025
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| Record UNII |
2KFI1XBH7G
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
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Common Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
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EPA PESTICIDE CODE |
67703
Created by
admin on Mon Mar 31 19:15:48 GMT 2025 , Edited by admin on Mon Mar 31 19:15:48 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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PINDONE
Created by
admin on Mon Mar 31 19:15:48 GMT 2025 , Edited by admin on Mon Mar 31 19:15:48 GMT 2025
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PRIMARY | |||
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6732
Created by
admin on Mon Mar 31 19:15:48 GMT 2025 , Edited by admin on Mon Mar 31 19:15:48 GMT 2025
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PRIMARY | |||
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1756
Created by
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PRIMARY | |||
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DTXSID1025930
Created by
admin on Mon Mar 31 19:15:48 GMT 2025 , Edited by admin on Mon Mar 31 19:15:48 GMT 2025
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PRIMARY | |||
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83-26-1
Created by
admin on Mon Mar 31 19:15:48 GMT 2025 , Edited by admin on Mon Mar 31 19:15:48 GMT 2025
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PRIMARY | |||
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31211
Created by
admin on Mon Mar 31 19:15:48 GMT 2025 , Edited by admin on Mon Mar 31 19:15:48 GMT 2025
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PRIMARY | |||
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2KFI1XBH7G
Created by
admin on Mon Mar 31 19:15:48 GMT 2025 , Edited by admin on Mon Mar 31 19:15:48 GMT 2025
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PRIMARY | |||
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C014152
Created by
admin on Mon Mar 31 19:15:48 GMT 2025 , Edited by admin on Mon Mar 31 19:15:48 GMT 2025
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PRIMARY | |||
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m8825
Created by
admin on Mon Mar 31 19:15:48 GMT 2025 , Edited by admin on Mon Mar 31 19:15:48 GMT 2025
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PRIMARY | Merck Index | ||
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pindone
Created by
admin on Mon Mar 31 19:15:48 GMT 2025 , Edited by admin on Mon Mar 31 19:15:48 GMT 2025
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PRIMARY | |||
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201-462-8
Created by
admin on Mon Mar 31 19:15:48 GMT 2025 , Edited by admin on Mon Mar 31 19:15:48 GMT 2025
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PRIMARY |