Home Other Building Blocks 1-Methoxynaphthalene

1-Methoxynaphthalene

CAS No.:
2216-69-5
Catalog Number:
AG0032SN
Molecular Formula:
C11H10O
Molecular Weight:
158.1965
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$25
- +
100g
98%
In Stock USA
United States
$63
- +
500g
98%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG0032SN
Chemical Name:
1-Methoxynaphthalene
CAS Number:
2216-69-5
Molecular Formula:
C11H10O
Molecular Weight:
158.1965
MDL Number:
MFCD00003924
IUPAC Name:
1-methoxynaphthalene
InChI:
InChI=1S/C11H10O/c1-12-11-8-4-6-9-5-2-3-7-10(9)11/h2-8H,1H3
InChI Key:
NQMUGNMMFTYOHK-UHFFFAOYSA-N
SMILES:
COc1cccc2c1cccc2
EC Number:
218-696-1
UNII:
DG2EOL57LF
NSC Number:
5530
Properties
Complexity:
144  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
158.073g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
158.2g/mol
Monoisotopic Mass:
158.073g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
9.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.6  
Literature
Title Journal
The rates of charge separation and energy destructive charge recombination processes within an organic dyad in presence of metal-semiconductor core shell nanocomposites. Journal of nanoscience and nanotechnology 20120101
Engineering the production of major catechins by Escherichia coli carrying metabolite genes of Camellia sinensis. TheScientificWorldJournal 20120101
Experimental (FT-IR and FT-Raman), electronic structure and DFT studies on 1-methoxynaphthalene. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20110801
Design of H2O2-dependent oxidation catalyzed by hemoproteins. Metallomics : integrated biometal science 20110401
Production of novel antioxidative prenyl naphthalen-ols by combinational bioconversion with dioxygenase PhnA1A2A3A4 and prenyltransferase NphB or SCO7190. Bioscience, biotechnology, and biochemistry 20110101
Toxicity and inhibition of feeding and tunneling response of naphthalene and 10 derivatives on the formosan subterranean termite (Isoptera: Rhinotermitidae). Journal of economic entomology 20101201
Aromatic C-H bond hydroxylation by P450 peroxygenases: a facile colorimetric assay for monooxygenation activities of enzymes based on Russig's blue formation. Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry 20100901
Self-assembly of hybrid dendrons into doubly segregated supramolecular polyhedral columns and vesicles. Journal of the American Chemical Society 20100818
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. Journal of nanoscience and nanotechnology 20100101
Comparative studies on the DNA-binding properties of linear and angular dibenzoquinolizinium ions. The Journal of organic chemistry 20061027
Biotransformation of 1-naphthol by a strictly aquatic fungus. Current microbiology 20060301
An efficient carbonyl-alkene metathesis of bicyclic oxetanes: photoinduced electron transfer reduction of the Paternò-Büchi adducts from 2,3-dihydrofuran and aromatic aldehydes. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20060101
Stereoselectivity in the triplet decay of chiral benzophenone-naphthalene bichromophoric systems. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20040101
Reductive PET cycloreversion of oxetanes: singlet multiplicity, regioselectivity, and detection of olefin radical anion. The Journal of organic chemistry 20031226
Selective acylation of 2 methoxynaphthalene by large pore zeolites: catalyst selection through molecular modeling. Computational biology and chemistry 20030701
NMR and calculational studies on the regioselective lithiation of 1-methoxynaphthalene. Journal of the American Chemical Society 20020724
Biotransformation of phenanthrene and 1-methoxynaphthalene with Streptomyces lividans cells expressing a marine bacterial phenanthrene dioxygenase gene cluster. Bioscience, biotechnology, and biochemistry 20010801
Properties