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
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
135°C (18 mmHg)
Melting Point
63-67°C
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 |
