1-CARBETHOXYIMIDAZOLE

  • CAS:19213-72-0
  • purity:99%
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  • Molecular Formula:C6H8 N2 O2
  • Molecular Weight:140.142
  • Vapor Pressure:9.61E-08mmHg at 25°C 
  • Refractive Index:n20/D1.472 
  • Boiling Point:231.7°Cat760mmHg 
  • PKA:3.73±0.10(Predicted) 
  • Flash Point:90°C 
  • PSA:44.12000 
  • Density:1.17g/cm3 
  • LogP:0.88770 

1-CARBETHOXYIMIDAZOLE(Cas 19213-72-0) Usage

General Description

1-Carbethoxyimidazole, also called Ethyl isocyanimidate, is a chemical compound with the molecular formula C4 H6 N2 O2. It exists as a light yellow to off-white powder with a melting point between 44-48°C. The compound is not known to occur naturally and is predominantly used in the field of organic chemistry, typically as a precursor or intermediate in the synthesis of more complex chemical compounds. Its specific properties, such as reactivity or toxicity, have not been well studied, indicating the need for careful handling and further research.

InChI:InChI=1/C13H9NOS/c14-9-16-8-13(15)12-6-5-10-3-1-2-4-11(10)7-12/h1-7H,8H2

19213-72-0 Relevant articles

A simple method for the functionalization of naked amino hydroxymethylenebisphosphonic acids via a carbamate bond

Lecouvey, Marc,Leroux, Yves

, p. 23 - 30 (2000)

A simple and efficient procedure for the...

Synthesis and properties of polymeric materials prepared by polymerization of epoxy oligomers with N,N′-carbonyldiimidazole transformation products

Fedoseev,Glushkov,Gorbunov,Derzhavinskaya,Oshchepkova

, p. 456 - 459 (2012)

The reaction of N,N′-carbonyldiimidazole...

Palladium-Catalyzed Oxidative C–H Alkoxycarbonylation of Arenes with Alkylcarbazates Directed by N-Heterocyclic Substituents

Yogesh Kumar, Gujjenahalli Ramalingaiah,Begum, Noor Shahina

supporting information, p. 4698 - 4704 (2020/07/04)

With alkyl carbazates as the green ester...

Method for preparing spiro2-diazido-indoline

-

Paragraph 0033; 0034; 0035, (2016/10/09)

The invention provides a method for prep...

Preparation method of spiro-2-azidoindoline

-

Paragraph 0045; 0046; 0047, (2016/10/10)

The invention provides a preparation met...

19213-72-0 Process route

ethanol
64-17-5

ethanol

1,1'-carbonyldiimidazole
530-62-1

1,1'-carbonyldiimidazole

1H-imidazole
288-32-4

1H-imidazole

ethyl 1-imidazolecarboxylate
19213-72-0

ethyl 1-imidazolecarboxylate

Conditions
Conditions Yield
In acetonitrile; at 25 ℃; for 12h;
95%
at 20 ℃;
1H-imidazole
288-32-4

1H-imidazole

ethyl 1-imidazolecarboxylate
19213-72-0

ethyl 1-imidazolecarboxylate

Conditions
Conditions Yield

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