2216-69-5 | 1-Methoxynaphthalene

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$14.00	$10.00
10g	98%	in stock	$15.00	$10.00
25g	98%	in stock	$23.00	$16.00
100g	98%	in stock	$36.00	$25.00
500g	98%	in stock	$116.00	$81.00

Description

• Catalog Number: AB43391
• Chemical Name: 1-Methoxynaphthalene
• CAS Number: 2216-69-5
• Molecular Formula: C11H10O
• Molecular Weight: 158.1965
• MDL Number: MFCD00003924
• SMILES: COc1cccc2c1cccc2
• NSC Number: 5530

Computed Properties

• Complexity: 144
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 3.6

Literature

• 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