2-Vinyl-1,3-dioxolane

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2-Vinyl-1,3-dioxolane

  • Name 2-Vinyl-1,3-dioxolane
  • CAS 3984-22-3
  • Purity 99%
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Product Details

Manufacturers supply cost-effective and customizable 2-Vinyl-1,3-dioxolane 3984-22-3

  • Molecular Formula: C5H8O2
  • Molecular Weight: 100.117
  • Appearance/Colour: Transparent colorless liquid 
  • Vapor Pressure: 56.5mmHg at 25°C 
  • Melting Point: 117°C 
  • Refractive Index: n20/D 1.431  
  • Boiling Point: 93.3 °C at 760 mmHg 
  • Flash Point: 21°C 
  • PSA: 18.46000 
  • Density: 1.092 g/cm3 
  • LogP: 0.54530 

2-Vinyl-1,3-dioxolane(Cas 3984-22-3) Usage

General Description

2-Vinyl-1,3-dioxolane is a colorless liquid chemical compound. It is commonly used as an intermediate in the production of pharmaceuticals and other organic compounds. This chemical has a sweet odor and is classified as a potential occupational carcinogen. It is considered to be a low hazard chemical with low acute toxicity, but prolonged exposure may cause skin and eye irritation. 2-Vinyl-1,3-dioxolane is primarily utilized in the chemical industry for the synthesis of various other compounds due to its reactivity and versatile properties.

InChI:InChI=1/C5H8O2/c1-2-5-6-3-4-7-5/h2,5H,1,3-4H2

3984-22-3 Relevant articles

Efficient synthesis of α-branched purine-based acyclic nucleosides: Scopes and limitations of the method

Dra?ínsky, Martin,Frydrych, Jan,Janeba, Zlatko,Slavětínská, Lenka Po?tová

, (2020/10/02)

An efficient route to acylated acyclic n...

Facile synthesis of acid-labile polymers with pendent ortho esters

Cheng, Jing,Ji, Ran,Gao, Shi-Juan,Du, Fu-Sheng,Li, Zi-Chen

experimental part, p. 173 - 179 (2012/04/23)

This work presents a facile approach for...

Method of preparing optically active alpha -amino acids and alpha -amino acid derivatives

-

, (2008/06/13)

PCT No. PCT/EP96/03984 Sec. 371 Date Apr...

Acetalization of α,β-unsaturated carbonyl compounds catalyzed by complexes of Pt(II)

Nieddu, Enrico,Cataldo, Maurizio,Pinna, Francesco,Strukul, Giorgio

, p. 6987 - 6990 (2007/10/03)

A class of cationic diphosphine complexe...

3984-22-3 Process route

ethylene glycol
107-21-1

ethylene glycol

acrolein
107-02-8,25068-14-8

acrolein

2-vinyl-1,3-dioxolane
3984-22-3

2-vinyl-1,3-dioxolane

Conditions
Conditions Yield
pyridinium p-toluenesulfonate; In diethyl ether; pentane; for 95h; Heating;
57%
With pyridinium p-toluenesulfonate; In diethyl ether; pentane; at 45 ℃; for 168h;
24%
monoaluminum phosphate; In acetonitrile; at 30 ℃; Thermodynamic data; E(a), ΔH(excit.), ΔS(excit.); var. catalysts and temp.;
[(1,4-bis(diphenylphosphino)butane)Pt(μ-OH)](BF4)2; In 1,2-dichloro-ethane; at 82 ℃; for 5h;
83 % Chromat.
With toluene-4-sulfonic acid; In toluene; at 120 ℃; for 6h;
acrolein
107-02-8,25068-14-8

acrolein

2-vinyl-1,3-dioxolane
3984-22-3

2-vinyl-1,3-dioxolane

Conditions
Conditions Yield
In water; ethylene glycol; benzene;
89%

3984-22-3 Upstream products

  • 107-21-1
    107-21-1

    ethylene glycol

  • 107-02-8
    107-02-8

    acrolein

  • 71-36-3
    71-36-3

    butan-1-ol

3984-22-3 Downstream products

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    146848-99-9

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  • 119124-31-1
    119124-31-1

    4-(2-Hydroxy-ethoxy)-1-phenyl-hex-5-en-3-ol

  • 89709-99-9
    89709-99-9

    5-carbethoxy-2H,3H,5H,6H-1,4-dioxocin

  • 773094-08-9
    773094-08-9

    2-carbethoxy-1-cyclopropanecarboxaldehyde ethylene acetal

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