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
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 |
|
| Selective acylation of 2 methoxynaphthalene by large pore zeolites: catalyst selection through molecular modeling. | 2003 Jul |
|
| Stereoselectivity in the triplet decay of chiral benzophenone-naphthalene bichromophoric systems. | 2004 Jan |
|
| 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
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID5062263
Created by
admin on Fri Dec 15 18:02:47 GMT 2023 , Edited by admin on Fri Dec 15 18:02:47 GMT 2023
|
PRIMARY | |||
|
16668
Created by
admin on Fri Dec 15 18:02:47 GMT 2023 , Edited by admin on Fri Dec 15 18:02:47 GMT 2023
|
PRIMARY | |||
|
218-696-1
Created by
admin on Fri Dec 15 18:02:47 GMT 2023 , Edited by admin on Fri Dec 15 18:02:47 GMT 2023
|
PRIMARY | |||
|
2216-69-5
Created by
admin on Fri Dec 15 18:02:47 GMT 2023 , Edited by admin on Fri Dec 15 18:02:47 GMT 2023
|
PRIMARY | |||
|
DG2EOL57LF
Created by
admin on Fri Dec 15 18:02:47 GMT 2023 , Edited by admin on Fri Dec 15 18:02:47 GMT 2023
|
PRIMARY | |||
|
5530
Created by
admin on Fri Dec 15 18:02:47 GMT 2023 , Edited by admin on Fri Dec 15 18:02:47 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
