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2216-69-5,MFCD00003924
Catalog No.:AA0032PV

2216-69-5 | 1-Methoxynaphthalene

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10g
98%
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$6.00   $4.00
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25g
98%
in stock  
$13.00   $9.00
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100g
98%
in stock  
$18.00   $13.00
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500g
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0032PV
Chemical Name:
1-Methoxynaphthalene
CAS Number:
2216-69-5
Molecular Formula:
C11H10O
Molecular Weight:
158.1965
MDL Number:
MFCD00003924
SMILES:
COc1cccc2c1cccc2
NSC Number:
5530
Properties
Properties
 
BP:
268.3°C at 760 mmHg  
Form:
Liquid  
MP:
5 °C  
Refractive Index:
n20/D 1.621(lit.)  
Storage:
Inert atmosphere;Room Temperature;  

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

Title: The rates of charge separation and energy destructive charge recombination processes within an organic dyad in presence of metal-semiconductor core shell nanocomposites.

Journal: Journal of nanoscience and nanotechnology 20120101

Title: Engineering the production of major catechins by Escherichia coli carrying metabolite genes of Camellia sinensis.

Journal: TheScientificWorldJournal 20120101

Title: Experimental (FT-IR and FT-Raman), electronic structure and DFT studies on 1-methoxynaphthalene.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20110801

Title: Design of H2O2-dependent oxidation catalyzed by hemoproteins.

Journal: Metallomics : integrated biometal science 20110401

Title: Production of novel antioxidative prenyl naphthalen-ols by combinational bioconversion with dioxygenase PhnA1A2A3A4 and prenyltransferase NphB or SCO7190.

Journal: Bioscience, biotechnology, and biochemistry 20110101

Title: Toxicity and inhibition of feeding and tunneling response of naphthalene and 10 derivatives on the formosan subterranean termite (Isoptera: Rhinotermitidae).

Journal: Journal of economic entomology 20101201

Title: Aromatic C-H bond hydroxylation by P450 peroxygenases: a facile colorimetric assay for monooxygenation activities of enzymes based on Russig's blue formation.

Journal: Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry 20100901

Title: Self-assembly of hybrid dendrons into doubly segregated supramolecular polyhedral columns and vesicles.

Journal: Journal of the American Chemical Society 20100818

Title: 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: Journal of nanoscience and nanotechnology 20100101

Title: Comparative studies on the DNA-binding properties of linear and angular dibenzoquinolizinium ions.

Journal: The Journal of organic chemistry 20061027

Title: Biotransformation of 1-naphthol by a strictly aquatic fungus.

Journal: Current microbiology 20060301

Title: An efficient carbonyl-alkene metathesis of bicyclic oxetanes: photoinduced electron transfer reduction of the Paternò-Büchi adducts from 2,3-dihydrofuran and aromatic aldehydes.

Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20060101

Title: Stereoselectivity in the triplet decay of chiral benzophenone-naphthalene bichromophoric systems.

Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20040101

Title: Reductive PET cycloreversion of oxetanes: singlet multiplicity, regioselectivity, and detection of olefin radical anion.

Journal: The Journal of organic chemistry 20031226

Title: Selective acylation of 2 methoxynaphthalene by large pore zeolites: catalyst selection through molecular modeling.

Journal: Computational biology and chemistry 20030701

Title: NMR and calculational studies on the regioselective lithiation of 1-methoxynaphthalene.

Journal: Journal of the American Chemical Society 20020724

Title: Biotransformation of phenanthrene and 1-methoxynaphthalene with Streptomyces lividans cells expressing a marine bacterial phenanthrene dioxygenase gene cluster.

Journal: Bioscience, biotechnology, and biochemistry 20010801

Title: Erman JE, et, al. Peroxygenase activity of cytochrome c peroxidase and three apolar distal heme pocket mutants: hydroxylation of 1-methoxynaphthalene. BMC Biochem. 2013 Jul 30;14:19.

Title: Shindo K, et, al. Production of novel antioxidative prenyl naphthalen-ols by combinational bioconversion with dioxygenase PhnA1A2A3A4 and prenyltransferase NphB or SCO7190. Biosci Biotechnol Biochem. 2011;75(3):505-10.

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