2-Vinylnaphthalene

Product Information

Molecular Formula:
C12H10
Molecular Weight:
154.21
Description
2-Vinylnaphthalene is employed in plastic scintillators, neutron detectors and other demanding device applications.
Synonyms
VINYLNAPHTHALENE-2; 2-EthenyInaphthalene; 2-ethenyl-naphthalen; 2-ethenylnaphthalene; 2-VINYLNAPHTHALENE; BETA-VINYLNAPHTHALENE; 2-VINYLNAPHTHALENE, 99+%; 2-VINYLNAPHTHALIN 98%
IUPAC Name
2-ethenylnaphthalene
Canonical SMILES
C=CC1=CC2=CC=CC=C2C=C1
InChI
InChI=1S/C12H10/c1-2-10-7-8-11-5-3-4-6-12(11)9-10/h2-9H,1H2
InChI Key
KXYAVSFOJVUIHT-UHFFFAOYSA-N
Boiling Point
135ºC (18 mmHg)
Melting Point
63-67ºC
Flash Point
Not applicable
Purity
98%
Density
1.031 g/cm3
Appearance
White to light beige crystalline powder.
Storage
Keep Cold

Safety Information

Hazards
H371
Precautionary Statement
P308 + P311

Computed Properties

XLogP3
4.3
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
1
Exact Mass
154.078250319 g/mol
Monoisotopic Mass
154.078250319 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
12
Formal Charge
0
Complexity
159
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113862708-A Method for electrochemically synthesizing beta-cyano-bis-phenylsulfonyl imide compound 2021-11-03
CN-114149300-A Synthesis method of copper-catalyzed trifluoromethyl allene compound 2021-11-01
CN-113860984-A Magnesium-activated ligand-promoted chromium-catalyzed polycyclic aromatic hydrocarbon and olefin regioselective hydrogenation method 2021-10-09
CN-113683633-A Preparation method of alkyl borate 2021-08-31
CN-113651855-A Novel loaded crystalline porous framework material and preparation method and application thereof 2021-08-19
CN-113549659-A Method for preparing beta-halogenated ether and beta-halogenated alcohol by peroxidase catalysis 2021-07-27
CN-113548936-A Aroyldifluoromethyl olefin and preparation method thereof 2021-07-13
CN-113429272-A Aryl aldehyde ketone and synthetic method thereof 2021-06-21
CN-113307749-A Method for synthesizing beta-ketosulfone derivative under mild condition and obtained beta-ketosulfone derivative 2021-05-26
CN-113278210-A Rubber-plastic alloy for modified asphalt mixture and preparation method thereof 2021-05-19

Literatures

PMID Publication Date Title Journal
21206083 2011-01-01 2-Bromo-1,3-bis[2-(2-naphthyl)vinyl]benzene benzene hemisolvate and 9-bromodinaphth[1,2-a:2',1'-j]anthracene Acta crystallographica. Section C, Crystal structure communications
20621497 2010-08-01 Synthesis and biological evaluation of arylidene analogues of Meldrum's acid as a new class of antimalarial and antioxidant agents Bioorganic & medicinal chemistry
17047810 2006-09-21 Expanding the useful range of ionic liquids: melting point depression of organic salts with carbon dioxide for biphasic catalytic reactions Chemical communications (Cambridge, England)
16257731 2005-11-01 Preparation of a novel fluorescence nanoparticles and its application in the determination of Hg(II) Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
14624571 2003-11-26 Intermolecular, markovnikov hydroamination of vinylarenes with alkylamines Journal of the American Chemical Society
11933085 2002-04-02 Metalloporphyrin-mediated asymmetric nitrogen-atom transfer to hydrocarbons: aziridination of alkenes and amidation of saturated C-H bonds catalyzed by chiral ruthenium and manganese porphyrins Chemistry (Weinheim an der Bergstrasse, Germany)
4893 1975-11-01 Clinical experience with beta-blockers in consultant psychiatric practice Scottish medical journal
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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