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827-54-3

2-Vinylnaphthalene

2-Vinylnaphthalene

別名:
CasNo.: 827-54-3
分子式: C12H10
分子量: 154.211
儲存條件:
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中文名稱: 2-Vinylnaphthalene
英文名稱: 2-Vinylnaphthalene
CasNo.: 827-54-3
分子式: C12H10
分子量: 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 white powder with a sweet, floral odor; 

2-Vinylnaphthalene is an important organic compound with a wide range of applications in multiple fields:

Synthesis of high-performance polymers: It serves as a monomer for the synthesis of various polymers with excellent properties. For example, by copolymerizing with other monomers, copolymers with special properties can be prepared, and these polymers are widely used in the fields of plastics, rubber, etc. Through polymerization with suitable monomers, materials with good mechanical properties, thermal stability, and chemical corrosion resistance can be obtained, which can be used for manufacturing auto parts, electronic device casings, and so on.
Preparation of special resins: It is a key raw material for the production of vinyl naphthalene resins. Vinyl naphthalene resins have unique physical and chemical properties, such as good solubility, film-forming property, and adhesiveness. These resins can be applied in industries such as coatings and adhesives, which can improve the performance and quality of products. For instance, in coatings, they can enhance the adhesion and durability of the coating.
In the field of photoresists: In the semiconductor lithography process, 2-vinylnaphthalene and its derivatives can be used to prepare photoresists. Photoresists are key materials in semiconductor manufacturing and are crucial for accurately replicating circuit patterns. The introduction of 2-vinylnaphthalene can improve the photosensitive performance, resolution, and corrosion resistance of photoresists, meeting the higher requirements for photoresist performance in the continuous development of the semiconductor industry.
Pharmaceutical intermediates: In drug synthesis, 2-vinylnaphthalene can serve as an important intermediate. Its unique molecular structure provides a basis for the synthesis of drug molecules with specific biological activities. By chemically modifying and reacting 2-vinylnaphthalene, various compounds with potential medicinal values can be prepared for the development of drugs for treating dif

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

  • 939-27-5
    939-27-5

    2-ethylnaphthalene

  • 1485-07-0
    1485-07-0

    naphthalen-2-ethanol

  • 32298-46-7
    32298-46-7

    2,2'-(ethane-1,1-diyl)dinaphthalene

  • 22364-54-1
    22364-54-1

    naphthalen-2-yl(trimethylsilyl)methanone

827-54-3 Downstream products

  • 143879-48-5
    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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