Details
Stereochemistry | RACEMIC |
Molecular Formula | C9H6Cl3O3.Na |
Molecular Weight | 291.491 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].CC(OC1=C(Cl)C=C(Cl)C(Cl)=C1)C([O-])=O
InChI
InChIKey=UMJWXKDMIKWUJC-UHFFFAOYSA-M
InChI=1S/C9H7Cl3O3.Na/c1-4(9(13)14)15-8-3-6(11)5(10)2-7(8)12;/h2-4H,1H3,(H,13,14);/q;+1/p-1
Molecular Formula | Na |
Molecular Weight | 22.9898 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C9H6Cl3O3 |
Molecular Weight | 268.501 |
Charge | -1 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Differential effect of peroxisome proliferators on rat glutathione S-transferase isoenzymes. | 1996 Oct |
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Molecularly imprinted solid-phase extraction sorbent for the clean-up of chlorinated phenoxyacids from aqueous samples. | 2001 Dec 14 |
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Automated dynamic liquid-liquid-liquid microextraction followed by high-performance liquid chromatography-ultraviolet detection for the determination of phenoxy acid herbicides in environmental waters. | 2005 Aug 5 |
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Determination of pharmaceuticals, iodinated contrast media and musk fragrances in sludge by LC/tandem MS and GC/MS. | 2005 Mar 4 |
|
Chirally functionalized anion-exchange type silica monolith for enantiomer separation of 2-aryloxypropionic acid herbicides by non-aqueous capillary electrochromatography. | 2009 Nov |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:08:10 GMT 2023
by
admin
on
Sat Dec 16 09:08:10 GMT 2023
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Record UNII |
EV52L8X6DP
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Record Status |
Validated (UNII)
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Record Version |
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-
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EPA PESTICIDE CODE |
82504
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EV52L8X6DP
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37913-89-6
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DTXSID4042387
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23719550
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253-714-1
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