Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H14O |
Molecular Weight | 246.3032 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=C(C=CC=C1C2=CC=CC=C2)C3=CC=CC=C3
InChI
InChIKey=ATGFTMUSEPZNJD-UHFFFAOYSA-N
InChI=1S/C18H14O/c19-18-16(14-8-3-1-4-9-14)12-7-13-17(18)15-10-5-2-6-11-15/h1-13,19H
Approval Year
PubMed
Title | Date | PubMed |
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Chiral molecular recognition by aluminum tris(2,6-diphenylphenoxide) in an asymmetric 1,4-addition. | 2004 Feb 13 |
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Clathrate formation from octaazaphthalocyanines possessing bulky phenoxyl substituents: a new cubic crystal containing solvent-filled, nanoscale voids. | 2008 |
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Substrate encapsulation: an efficient strategy for the RCM synthesis of unsaturated epsilon-lactones. | 2008 Dec 18 |
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Developments in heterobimetallic s-block systems: synthesis and structural survey of molecular M/Ae (M=Li, Na, K, Cs; Ae=Ca, Sr) aryloxo complexes. | 2008 Jun 2 |
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Charge-separated and molecular heterobimetallic rare earth-rare earth and alkaline earth-rare earth aryloxo complexes featuring intramolecular metal-pi-arene interactions. | 2009 |
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Stereoselective construction of halogenated quaternary stereogenic centers via catalytic asymmetric Diels-Alder reaction. | 2010 Apr 28 |
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Experimental and computational studies into an ATPH-promoted exo-selective IMDA reaction: a short total synthesis of Delta9-THC. | 2010 Jul 26 |
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Enhancement of incident photon-to-current conversion efficiency for phthalocyanine-sensitized solar cells by 3D molecular structuralization. | 2010 Mar 31 |
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LA93W35M96
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DTXSID30947151
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75512
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219-401-9
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2432-11-3
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SUBSTANCE RECORD