Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H10O |
| Molecular Weight | 158.1965 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=CC2=C1C=CC=C2
InChI
InChIKey=NQMUGNMMFTYOHK-UHFFFAOYSA-N
InChI=1S/C11H10O/c1-12-11-8-4-6-9-5-2-3-7-10(9)11/h2-8H,1H3
| Molecular Formula | C11H10O |
| Molecular Weight | 158.1965 |
| 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 |
|---|---|---|
| Biotransformation of phenanthrene and 1-methoxynaphthalene with Streptomyces lividans cells expressing a marine bacterial phenanthrene dioxygenase gene cluster. | 2001 Aug |
|
| NMR and calculational studies on the regioselective lithiation of 1-methoxynaphthalene. | 2002 Jul 24 |
|
| Reductive PET cycloreversion of oxetanes: singlet multiplicity, regioselectivity, and detection of olefin radical anion. | 2003 Dec 26 |
|
| An efficient carbonyl-alkene metathesis of bicyclic oxetanes: photoinduced electron transfer reduction of the Paternò-Büchi adducts from 2,3-dihydrofuran and aromatic aldehydes. | 2006 Jan |
|
| Biotransformation of 1-naphthol by a strictly aquatic fungus. | 2006 Mar |
|
| Comparative studies on the DNA-binding properties of linear and angular dibenzoquinolizinium ions. | 2006 Oct 27 |
|
| Self-assembly of hybrid dendrons into doubly segregated supramolecular polyhedral columns and vesicles. | 2010 Aug 18 |
|
| Toxicity and inhibition of feeding and tunneling response of naphthalene and 10 derivatives on the formosan subterranean termite (Isoptera: Rhinotermitidae). | 2010 Dec |
|
| Development of a nanocomposite system by combining an organic dyad 1-(4-chloro-phenyl)-3-(4-methoxy-naphthalen-1-yl)-Propenone with semiconductor TiO2 nanoparticles. | 2010 Jan |
|
| Aromatic C-H bond hydroxylation by P450 peroxygenases: a facile colorimetric assay for monooxygenation activities of enzymes based on Russig's blue formation. | 2010 Sep |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:02:47 GMT 2023
by
admin
on
Fri Dec 15 18:02:47 GMT 2023
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| Record UNII |
DG2EOL57LF
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| Record Status |
Validated (UNII)
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| Record Version |
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