Vinylimidazole

Basic information

  • Product Name:Vinylimidazole
  • CasNo.:1072-63-5
  • MF:C5H6N2

Physical and Chemical Properties

  • Purity:99%
  • Melting Point:78-79 ºC
  • Appearance:Colorless to faint yellow transparent liquid
Inquiry

Product Details

CasNo: 1072-63-5

MF: C5H6N2

Appearance: Colorless to faint yellow transparent liquid

Factory sells Vinylimidazole 1072-63-5 with sufficient production capacity

  • Molecular Formula:C5H6N2
  • Molecular Weight:94.116
  • Appearance/Colour:Colorless to faint yellow transparent liquid 
  • Vapor Pressure:0.506mmHg at 25°C 
  • Melting Point:78-79 ºC 
  • Refractive Index:n20/D 1.533(lit.)  
  • Boiling Point:191.8 ºC at 760 mmHg 
  • PKA:6.07±0.10(Predicted) 
  • Flash Point:69.8 ºC 
  • PSA:17.82000 
  • Density:1.038 g/cm3 
  • LogP:0.98360 

Vinylimidazole(Cas 1072-63-5) Usage

Description Vinylimidazole is an organic compound belonging to the imidazole family, characterized by a vinyl group attached to the nitrogen-containing imidazole ring.

Flammability and Explosibility

Notclassified

Uses Vinylimidazole is notable for its reactivity, particularly in polymer chemistry, where it serves as a monomer or a co-monomer in the synthesis of polymers and copolymers with specific properties. Its imidazole ring endows it with unique basicity and nucleophilicity, making it useful in various chemical reactions and applications, including as a curing agent for epoxy resins and as a component in adhesives, coatings, and sealants. Vinylimidazole also finds utility in biomedical applications, where its polymers can be tailored for drug delivery systems, hydrogels, and bioadhesives, demonstrating the compound's versatility and importance in both industrial and medical fields.

InChI:InChI=1/C5H6N2/c1-2-7-4-3-6-5-7/h2-5H,1H2

1072-63-5 Relevant articles

Highly Recoverable Pd(II) Catalysts for the Mizoroki-Heck Reaction Based on N-Heterocyclic Carbenes and Poly(benzyl ether) Dendrons

Ortiz, Alba,Gómez-Sal, Pilar,Flores, Juan C.,De Jesús, Ernesto

, p. 3598 - 3610 (2018)

Two series of bis(imidazolylidene)pallad...

Theoretical prediction and electrochemical evaluation of vinylimidazole and allylimidazole as corrosion inhibitors for mild steel in 1 M HCl

I.B. Obot a , S.A. Umoren a , Z.M. Gasem a , Rami Suleiman a , Bassam El Ali b

, Journal of Industrial and Engineering Chemistry Volume 21 , 25 January 2015, Pages 1328-1339

Nyuist plot of steel corrosion in 1 M HCl in the absence and presence of vinylimidazole (VI) and equilibrium adsorption configurations of VI on Fe2O3 (0 1 0) surface using molecular dynamics (MD) simulations.

Solvent-free copper/iron co-catalyzed N-arylation reactions of nitrogen-containing heterocycles with trimethoxysilanes in air

Song, Ren-Jie,Deng, Chen-Liang,Xie, Ye-Xiang,Li, Jin-Heng

, p. 7845 - 7848 (2007)

A solvent-free copper/iron-catalyzed N-a...

1072-63-5 Process route

1-vinylimidazole
1072-63-5,25232-42-2

1-vinylimidazole

propylphosphonic dichloride
4708-04-7

propylphosphonic dichloride

Conditions
Conditions Yield
 
 
1H-imidazole
288-32-4

1H-imidazole

acetylene
74-86-2,25067-58-7

acetylene

1-vinylimidazole
1072-63-5,25232-42-2

1-vinylimidazole

Conditions
Conditions Yield
With potassium hydroxide; In 1,4-dioxane;
70%
With copper dichloride; In various solvent(s); at 180 ℃; for 20h; under 76 - 380 Torr;
65%
With tributylphosphine; In N,N-dimethyl acetamide; at 140 ℃; for 16h; under 1.5 Torr; Glovebox; Sealed tube; Autoclave;
65%
copper(l) chloride; In various solvent(s); for 28h; Product distribution; various time, acetylene sparging, packing diameter,;
89 % Chromat.
With 1,4-dioxane; nitrogen; potassium 1H-imidazolide; unter Zusatz von KOH und ZnO;
 
base; Purification / work up;
 
 
 

1072-63-5 Upstream products

  • 288-32-4
    288-32-4

    1H-imidazole

  • 74-86-2
    74-86-2

    acetylene

  • 107-06-2
    107-06-2

    1,2-dichloro-ethane

  • 106-93-4
    106-93-4

    ethylene dibromide

1072-63-5 Downstream products

  • 45662-46-2
    45662-46-2

    1-vinyl-2-hydroxymethylimidazole

  • 92234-41-8
    92234-41-8

    5-(1-imidazolyl)-3-(4-methoxyphenyl)-2-phenylisoxazolidine

  • 92234-43-0
    92234-43-0

    methyl 5-(1-imidazolyl)-2,3-diphenylisoxazolidine-4-carboxylate

  • 92234-40-7
    92234-40-7

    5-(1-imidazolyl)-3-(4-methylphenyl)-2-phenylisoxazolidine