Details
Stereochemistry | ACHIRAL |
Molecular Formula | C13H12O2 |
Molecular Weight | 200.2332 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=C(CC2=CC=C(O)C=C2)C=C1
InChI
InChIKey=PXKLMJQFEQBVLD-UHFFFAOYSA-N
InChI=1S/C13H12O2/c14-12-5-1-10(2-6-12)9-11-3-7-13(15)8-4-11/h1-8,14-15H,9H2
Molecular Formula | C13H12O2 |
Molecular Weight | 200.2332 |
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 |
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Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens. | 2001 Mar |
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[2,6-Bis[(dimethylamino)methyl]pyridine-kappa3N](2,2-methylenediphenolato-kappa2O,O')dioxouranium(VI) acetone solvate. | 2004 Nov |
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Dinuclear complexes of a pseudocalixarene macrocycle: structural consequences of intramolecular hydrogen bonding. | 2005 Mar 7 |
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Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. | 2006 Nov |
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Conformational isomerization and collisional cooling dynamics of bis(2-hydroxyphenyl)methane. | 2009 Apr 30 |
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Conformational effects on excitonic interactions in a prototypical H-bonded bichromophore: bis(2-hydroxyphenyl)methane. | 2009 Apr 30 |
|
Synthesis and antimicrobial activities of halogenated bis(hydroxyphenyl)methanes. | 2009 Feb 1 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:08:34 GMT 2023
by
admin
on
Fri Dec 15 15:08:34 GMT 2023
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Record UNII |
QD2C19044Z
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Record Status |
Validated (UNII)
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Record Version |
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