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Sigma-Aldrich

1-Vinylnaphthalene

95%

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About This Item

Linear Formula:
C10H7CH=CH2
CAS Number:
826-74-4
Molecular Weight:
154.21
MDL number:
MFCD00075766
UNSPSC Code:
12352103
PubChem Substance ID:
24877761
NACRES:
NA.23

Assay

95%

contains

3000 ppm tert-butylcatechol as inhibitor

impurities

≤2% poly(1-vinylnaphthalene)

refractive index

n20/D 1.653 (lit.)

bp

135-138 °C (lit.)

density

1.04 g/mL at 25 °C (lit.)

storage temp.

−20°C

SMILES string

C=Cc1cccc2ccccc12

InChI

1S/C12H10/c1-2-10-7-5-8-11-6-3-4-9-12(10)11/h2-9H,1H2

InChI key

IGGDKDTUCAWDAN-UHFFFAOYSA-N

Application

1-Vinylnaphthalene may be used in the synthesis of 1-naphthyl-1,2-ethanediol, which can further be utilized as a metal hydrogenated catalyst. It may also be used as a substrate material to produce azidocyanation based products.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 2

Flash Point(F)

213.8 °F

Flash Point(C)

101 °C

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Modulation of Trehalose Dimycolate and Immune System by Rv0774c Protein Enhanced the Intracellular Survival of
Arbind Kumar et al.
Frontiers in cellular and infection microbiology, 7, 289-289 (2017-07-18)
1-Naphthyl-1, 2-ethanediol as a new chiral modifier of platinum in the enantioselective hydrogenation of activated ketones.
Marinas A, et al.
J. Catal., 221(2), 666-669 (2004)
Rana Dhar et al.
Immunopharmacology and immunotoxicology, 40(1), 43-51 (2017-12-05)
Immune dysregulation has been implicated in the pathogenesis of many diseases. Macrophages play a crucial role contributing to the onset, progression, and resolution of inflammation. Macrophage inflammatory mediators are of considerable interest as potential targets to treat inflammatory diseases. The
Enantioselective Copper-Catalyzed Intermolecular Amino-and Azidocyanation of Alkenes in a Radical Process.
Wang D, et al.
Angewandte Chemie (International Edition in English), 56(8), 2054-2058 (2017)

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