1-Methoxynaphthalene - CAS 2216-69-5

Catalog:	BB017433
Product Name:	1-Methoxynaphthalene
CAS:	2216-69-5
Synonyms:	1-methoxynaphthalene

Technical Data

Patents

Literatures

Computed Properties

IUPAC Name:	1-methoxynaphthalene
Description:	1-Methoxynaphthalene (CAS# 2216-69-5) is one of the numerous volatile components found in tobacco smoke, and has been found to induce damage on plasma membrane tissues of cultured human lung fibroblasts.
Molecular Weight:	158.20
Molecular Formula:	C11H10O
Canonical SMILES:	COC1=CC=CC2=CC=CC=C21
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
Boiling Point:	135-137 °C (12 mmHg)
Purity:	97 %
Density:	1.09 g/cm³
Appearance:	Clear light yellow to brown liquid
MDL:	MFCD00003924
LogP:	2.84840

Publication Number	Title	Priority Date
JP-6942404-B1	Power generation elements, power generation equipment, electronic devices, power generation methods, and manufacturing methods of power generation elements	20210705
CN-113130853-A	Modified alkali metal ion battery negative plate, preparation method and application thereof	20210419
CN-113087725-A	Diazosulfide deuterated derivative and application thereof in organic electronic device	20210406
CN-113072563-A	Benzotriazole deuterated derivative and application thereof in organic electronic device	20210331
CN-112574011-A	One-pot synthesis method of substituted indane compounds	20201231

PMID	Publication Date	Title	Journal
22523964	20120101	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
22645428	20120101	Engineering the production of major catechins by Escherichia coli carrying metabolite genes of Camellia sinensis	TheScientificWorldJournal
21530378	20110801	Experimental (FT-IR and FT-Raman), electronic structure and DFT studies on 1-methoxynaphthalene	Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
21308129	20110401	Design of H2O2-dependent oxidation catalyzed by hemoproteins	Metallomics : integrated biometal science
21389612	20110101	Production of novel antioxidative prenyl naphthalen-ols by combinational bioconversion with dioxygenase PhnA1A2A3A4 and prenyltransferase NphB or SCO7190	Bioscience, biotechnology, and biochemistry

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Related Functional Groups

Oxygen Compounds

[1281984-38-0]
1-Cyclopentyl-3,5-dinitro-1H-pyrazole
[202288-73-1]
2-(Pyridin-3-ylmethoxy)aniline dihydrochloride
[1183749-69-0]
2-(pyrimidin-2-yloxy)phenol
[832740-55-3]
3-[(4-Chloro-2-methylphenoxy)methyl]-4-methoxybenzaldehyde
[937601-34-8]
3-Bromo-2,5-dimethylpyrazolo[1,5-a]pyrimidine-7-carboxylic acid
[13566-71-7]
4(3H)-Pyrimidinone,6-hydroxy-2-phenyl-

Complexity:	144
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	158.073164938
Formal Charge:	0
Heavy Atom Count:	12
Hydrogen Bond Acceptor Count:	1
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	158.073164938
Rotatable Bond Count:	1
Topological Polar Surface Area:	9.2
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	3.6