827-54-3

2-Vinylnaphthalene

2-Vinylnaphthalene

Another Name:
CasNo.: 827-54-3
MF: C12H10
MW: 154.211
Storage:
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ch_Name: 2-Vinylnaphthalene
English name: 2-Vinylnaphthalene
CasNo.: 827-54-3
MF: C12H10
MW: 154.211

Factory sells 2-Vinylnaphthalene 827-54-3 with sufficient production capacity

  • Molecular Formula:C12H10
  • Molecular Weight:154.211
  • Appearance/Colour:Tan powder 
  • Melting Point:64-68 °C(lit.) 
  • Boiling Point:270.9 °C at 760 mmHg 
  • Flash Point:115.5 °C 
  • PSA:0.00000 
  • Density:1.031 g/cm3 
  • LogP:3.48280 

2-Vinylnaphthalene(Cas 827-54-3) Usage

General Description

2-Vinylnaphthalene, also known as 2-vinyl-1-naphthalene, is a chemical compound with the formula C12H10. It is a colorless liquid with a sweet, floral odor and is used in the production of plastics and resins. 2-Vinylnaphthalene is a vinylated naphthalene, meaning it has a vinyl group attached to the naphthalene ring. It is used as a precursor in the synthesis of various polymers and as a monomer for the production of vinyl naphthalene resins. It is also used as an intermediate in the manufacturing of pharmaceuticals and fragrances. However, 2-Vinylnaphthalene is also a potential irritant and can cause skin and eye irritation upon contact, as well as harmful effects if inhaled.

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

827-54-3 Relevant articles

Photoredox Catalyzed Sulfonylation of Multisubstituted Allenes with Ru(bpy)3Cl2 or Rhodamine B

Chen, Jingyun,Chen, Shufang,Jiang, Jun,Lu, Qianqian,Shi, Liyang,Xu, Zekun,Yimei, Zhao

supporting information, (2021/11/09)

A highly regio- and stereoselective sulf...

Functionalized styrene synthesis via palladium-catalyzed C[sbnd]C cleavage of aryl ketones

Dai, Hui-Xiong,Wang, Xing,Wang, Zhen-Yu,Xu, Hui,Zhang, Xu

supporting information, (2022/03/31)

We report herein the synthesis of functi...

Palladium-Catalyzed Benzylic Silylation of Diarylmethyl Carbonates with Silylboranes under Base-Free Conditions

Asai, Kento,Hirano, Koji,Miura, Masahiro

supporting information, (2022/02/19)

A palladium-catalyzed benzylic silylatio...

Copper-Catalyzed Sulfonylation of Cyclobutanone Oxime Esters with Sulfonyl Hydrazides

Dong, Bingbing,Lu, Jiansha,Bao, Honghao,Zhang, Yuanyuan,Liu, Yingguo,Leng, Yuting

supporting information, p. 3769 - 3776 (2021/07/14)

A copper-catalyzed radical cross-couplin...

827-54-3 Process route

dimethylsulfone
67-71-0

dimethylsulfone

2-Naphthalenemethanol
1592-38-7

2-Naphthalenemethanol

2-naphthylethylene
827-54-3,28406-56-6

2-naphthylethylene

hydrogen
1333-74-0

hydrogen

Conditions
Conditions Yield
With 1,10-Phenanthroline; potassium tert-butylate; iron(II) chloride; In toluene; at 120 ℃; for 24h; Inert atmosphere; Schlenk technique;
83%
cis-1,2,3,4,4a,9,10,10a-octahydrophenanthrene
64363-88-8

cis-1,2,3,4,4a,9,10,10a-octahydrophenanthrene

styrene
100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6

styrene

naphthalene
91-20-3,71998-51-1,72931-45-4

naphthalene

benzocyclobutene
694-87-1

benzocyclobutene

2-ethylnaphthalene
939-27-5

2-ethylnaphthalene

2-naphthylethylene
827-54-3,28406-56-6

2-naphthylethylene

2-Methylnaphthalene
91-57-6,34468-07-0

2-Methylnaphthalene

Conditions
Conditions Yield
at 860 ℃; under 0.1 Torr; Product distribution; other temp.;

827-54-3 Upstream products

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827-54-3 Downstream products

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    143879-48-5

    2-<2-(2-naphthyl)vinyl>acetanilide

  • 939-27-5
    939-27-5

    2-ethylnaphthalene

  • 136415-67-3
    136415-67-3

    3-(naphthalen-2-yl)propanal

  • 159759-69-0
    159759-69-0

    (R)-2-(naphthalen-2-yl)propanal

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