Details
Quality Factory Hot Selling 1-CARBETHOXYIMIDAZOLE 19213-72-0 with Fast Shipping
- 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
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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
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64-17-5
ethanol
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-
530-62-1
1,1'-carbonyldiimidazole
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-
288-32-4
1H-imidazole
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-
19213-72-0
ethyl 1-imidazolecarboxylate
| Conditions | Yield |
|---|---|
|
In
acetonitrile;
at 25 ℃;
for 12h;
|
95% |
|
at 20 ℃;
|
-
-
288-32-4
1H-imidazole
-
-
19213-72-0
ethyl 1-imidazolecarboxylate
| Conditions | Yield |
|---|---|
|
|
19213-72-0 Upstream products
-
288-32-4
1H-imidazole
-
541-41-3
chloroformic acid ethyl ester
-
63436-79-3
carbonic acid ethyl ester-isopropenyl ester
-
74877-64-8
ethyl α-methoxyvinyl carbonate
19213-72-0 Downstream products
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19673-86-0
1,3-dibenzyl-1H-imidazol-3-ium bromide
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86911-07-1
1-ethoxycarbonyl-3-<4-(2-methoxycarbonylvinyl)benzyl>imidazolium bromide
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58704-04-4
N,N'-dicarbethoxy-1,2-diaminoethene
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75144-32-0
N,N'-dicarbethoxy-N-formyl-1,2-diaminoethene
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