2,5-DIMETHYLSTYRENE

  • Name: 2,5-DIMETHYLSTYRENE
  • CAS: 2039-89-6
  • Purity: 99%
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Details

Factory Sells Best Quality 2,5-DIMETHYLSTYRENE 2039-89-6 with GMP standards

  • Molecular Formula: C10H12
  • Molecular Weight: 132.205
  • Vapor Pressure: 0.628mmHg at 25°C 
  • Melting Point: -35 °C 
  • Refractive Index: n20/D 1.539(lit.)  
  • Boiling Point: 194.1 °C at 760 mmHg 
  • Flash Point: 58.8 °C 
  • PSA： 0.00000 
  • Density: 0.893 g/cm3 
  • LogP: 2.94640 

2,5-DIMETHYLSTYRENE(Cas 2039-89-6) Usage

General Description

2,5-DIMETHYLSTYRENE is a chemical compound with the molecular formula C10H12. It is a colorless liquid with a distinct aromatic odor and is commonly used as a monomer in the production of polymers and plastics. 2,5-DIMETHYLSTYRENE is known for its high refractive index and is used in the production of optical lenses, adhesives, coatings, and sealants. It can also be used as a co-monomer in the production of specialty polymers, offering improved heat resistance and thermal stability. The chemical is considered to be a flammable liquid and should be handled with caution and stored in a well-ventilated area.

InChI:InChI=1/C10H12/c1-4-10-7-8(2)5-6-9(10)3/h4-7H,1H2,2-3H3

2039-89-6 Relevant articles

Nickel-Catalyzed Reductive Cross-Coupling of Aryl Bromides with Vinyl Acetate in Dimethyl Isosorbide as a Sustainable Solvent

Su, Mincong,Huang, Xia,Lei, Chuanhu,Jin, Jian

supporting information, p. 354 - 358 (2022/01/15)

A nickel-catalyzed reductive cross-coupl...

Iron-catalyzed, highly regioselective synthesis of α-aryl carboxylic acids from styrene derivatives and CO2

Greenhalgh, Mark D.,Thomas, Stephen P.

supporting information; experimental part, p. 11900 - 11903 (2012/09/07)

The iron-catalyzed hydrocarboxylation of...

Synthesis and characterization of aryl thioacetyl styrene monomers: towards a new generation of SERS-active polymers

Al-Hourani, Baker Jawabrah,Bravo-Vasquez, Juan P.,Hermann High,Fenniri, Hicham

, p. 9144 - 9147 (2008/09/17)

A new family of thioacetyl styrene deriv...

Pd2(dba)3/P(i-BuNCH2CH2) 3N-catalyzed Stille cross-coupling of aryl chlorides

Su, Weiping,Urgaonkar, Sameer,Verkade, John G.

, p. 1421 - 1424 (2007/10/03)

The Pd2(dba)3/P(i-BuNCH2CH 2)3N (1d) cat...

2039-89-6 Process route

2-chloro-1,4-dimethyl-benzene
95-72-7

2-chloro-1,4-dimethyl-benzene

tri-n-butyl(vinyl)tin
7486-35-3

tri-n-butyl(vinyl)tin

2,5-dimethylstyrene
2039-89-6

2,5-dimethylstyrene

Conditions
Conditions Yield
With tris(dibenzylideneacetone)dipalladium (0); tri-tert-butyl phosphine; cesium fluoride; In 1,4-dioxane; at 100 ℃; for 36h;
73%
With P(i-BuNCH2CH2)3N; tetramethylammonium fluoride; tris(dibenzylideneacetone)dipalladium (0); In 1,4-dioxane; at 100 - 110 ℃;
72%
With tri-tert-butyl phosphine; cesium fluoride; tris(dibenzylideneacetone)dipalladium (0); In 1,4-dioxane; at 100 ℃; for 36h;
71%
2,5-Dimethylphenyl-methyl-carbinol
32917-52-5

2,5-Dimethylphenyl-methyl-carbinol

2,5-dimethylstyrene
2039-89-6

2,5-dimethylstyrene

Conditions
Conditions Yield
With aluminum oxide; at 310 - 320 ℃; under 30 Torr;
With potassium hydrogensulfate; benzene-1,2-diol;

2039-89-6 Upstream products

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    10224-93-8

    1,1-bis-(2,5-dimethyl-phenyl)-ethane

  • 32917-52-5
    32917-52-5

    2,5-Dimethylphenyl-methyl-carbinol

  • 110663-93-9
    110663-93-9

    bis-[1-(2,5-dimethyl-phenyl)-ethyl]-ether

  • 95-72-7
    95-72-7

    2-chloro-1,4-dimethyl-benzene

2039-89-6 Downstream products

  • 1758-88-9
    1758-88-9

    2-ethyl-p-xylene

  • 57821-75-7
    57821-75-7

    5-(2,5-dimethylphenyl)dihydrofuran-2-one

  • 77403-89-5
    77403-89-5

    (E)-β-(2,5-dimethylphenyl)vinyl bromide

  • 6908-41-4
    6908-41-4

    4-(methoxycarbonyl)benzyl alcohol

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