Details
Stereochemistry | RACEMIC |
Molecular Formula | C19H15ClO4 |
Molecular Weight | 342.773 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)CC(C1=CC=C(Cl)C=C1)C2=C(O)C3=C(OC2=O)C=CC=C3
InChI
InChIKey=DEKWZWCFHUABHE-UHFFFAOYSA-N
InChI=1S/C19H15ClO4/c1-11(21)10-15(12-6-8-13(20)9-7-12)17-18(22)14-4-2-3-5-16(14)24-19(17)23/h2-9,15,22H,10H2,1H3
Molecular Formula | C19H15ClO4 |
Molecular Weight | 342.773 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Brush-type chiral stationary phase for enantioseparation of acidic compounds. Optimization of chiral capillary electrochromatographic parameters. | 2003 Jul 11 |
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Antihuman Immunodeficiency Virus Type 1 (HIV-1) Activity of Rare Earth Metal Complexes of 4-Hydroxycoumarins in Cell Culture. | 2006 |
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Synthesis, characterization, and cytotoxic activity of new lanthanum(III) complexes of bis-coumarins. | 2006 |
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Acute bromadiolone intoxication. | 2006 May |
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Separation and determination of warfarin enantiomers in human plasma using a novel polymeric surfactant for micellar electrokinetic chromatography-mass spectrometry. | 2007 Aug 3 |
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Achiral and chiral separations using MEKC, polyelectrolyte multilayer coatings, and mixed mode separation techniques with molecular micelles. | 2010 Mar |
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Characterization of warfarin unusual peak profiles on oligoproline chiral high performance liquid chromatography columns. | 2010 Oct 15 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:55:25 GMT 2023
by
admin
on
Sat Dec 16 08:55:25 GMT 2023
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Record UNII |
UCD8XZW42P
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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 |
224200
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m3814
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