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
| Molecular Formula | C18H14O |
| Molecular Weight | 246.3032 |
| 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 |
|---|---|---|
| Experimental and computational studies into an ATPH-promoted exo-selective IMDA reaction: a short total synthesis of Delta9-THC. | 2010-07-26 |
|
| Stereoselective construction of halogenated quaternary stereogenic centers via catalytic asymmetric Diels-Alder reaction. | 2010-04-28 |
|
| Enhancement of incident photon-to-current conversion efficiency for phthalocyanine-sensitized solar cells by 3D molecular structuralization. | 2010-03-31 |
|
| Metal-pi interactions dominate in the solid-state structures of molecular heterobimetallic alkali-metal-europium(II) aryloxo complexes. | 2009-08-03 |
|
| Charge-separated and molecular heterobimetallic rare earth-rare earth and alkaline earth-rare earth aryloxo complexes featuring intramolecular metal-pi-arene interactions. | 2009 |
|
| Substrate encapsulation: an efficient strategy for the RCM synthesis of unsaturated epsilon-lactones. | 2008-12-18 |
|
| Developments in heterobimetallic s-block systems: synthesis and structural survey of molecular M/Ae (M=Li, Na, K, Cs; Ae=Ca, Sr) aryloxo complexes. | 2008-06-02 |
|
| Clathrate formation from octaazaphthalocyanines possessing bulky phenoxyl substituents: a new cubic crystal containing solvent-filled, nanoscale voids. | 2008 |
|
| Synthesis of gamma-hydroxybutenolides applying crossed aldol condensation in the presence of a bulky lewis acid and their anti-tumor activity. | 2007-09 |
|
| Absolute asymmetric synthesis of stereochemically labile aldehyde helicates and subsequent chirality transfer reactions. | 2005-09-05 |
|
| Chiral molecular recognition by aluminum tris(2,6-diphenylphenoxide) in an asymmetric 1,4-addition. | 2004-02-13 |
|
| Synthesis, spectroscopic characterization and redox reactivity of some transition metal complexes with salicylaldimines bearing 2,6-di-phenylphenol. | 2004-01 |
|
| Synthesis of group 1 metal 2,6-diphenylphenoxide complexes [M(OC6H3Ph2-2,6)] (M = Li, Na, K, Rb, Cs) and structures of the solvent-free complexes [Rb(OC6H3Ph2-2,6)]x and [Cs(OC6H3Ph2-2,6)x: one-dimensional extended arrays of metal aryloxides. | 2003-09-22 |
|
| Molecular recognition of alpha,beta-unsaturated carbonyl compounds using aluminum tris(2,6-diphenylphenoxide) (ATPH): structural and conformational analysis of ATPH complexes and application to the selective vinylogous aldol reaction. | 2003-05-21 |
|
| Diverse heteroleptic ytterbium(III) thiocyanate complexes by oxidation from bis(thiocyanato)ytterbium(II). | 2001-04-17 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:02:32 GMT 2025
by
admin
on
Mon Mar 31 20:02:32 GMT 2025
|
| Record UNII |
LA93W35M96
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
LA93W35M96
Created by
admin on Mon Mar 31 20:02:32 GMT 2025 , Edited by admin on Mon Mar 31 20:02:32 GMT 2025
|
PRIMARY | |||
|
DTXSID30947151
Created by
admin on Mon Mar 31 20:02:32 GMT 2025 , Edited by admin on Mon Mar 31 20:02:32 GMT 2025
|
PRIMARY | |||
|
75512
Created by
admin on Mon Mar 31 20:02:32 GMT 2025 , Edited by admin on Mon Mar 31 20:02:32 GMT 2025
|
PRIMARY | |||
|
219-401-9
Created by
admin on Mon Mar 31 20:02:32 GMT 2025 , Edited by admin on Mon Mar 31 20:02:32 GMT 2025
|
PRIMARY | |||
|
2432-11-3
Created by
admin on Mon Mar 31 20:02:32 GMT 2025 , Edited by admin on Mon Mar 31 20:02:32 GMT 2025
|
PRIMARY |