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Ethyl carbazate, 97%
CAS: 4114-31-2 | C3H8N2O2 | 104.109 g/mol
$102.90 - $1012.95
Chemical Identifiers
CAS | 4114-31-2 |
---|---|
Molecular Formula | C3H8N2O2 |
Molecular Weight (g/mol) | 104.109 |
MDL Number | MFCD00007595 |
InChI Key | VYSYZMNJHYOXGN-UHFFFAOYSA-N |
Synonym | ethyl carbazate, ethyl hydrazinecarboxylate, ethoxycarbohydrazide, hydrazinecarboxylic acid, ethyl ester, carbethoxyhydrazine, ethylcarbazate, ethyl carbazinate, carboethoxyhydrazine, monocarbethoxyhydrazine, n-carbethoxy hydrazine |
PubChem CID | 20064 |
IUPAC Name | ethyl N-aminocarbamate |
SMILES | CCOC(=O)NN |
Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
AAA1386018
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Thermo Scientific Chemicals
A1386018 |
50 g |
Each for $102.90
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AAA1386030
|
Thermo Scientific Chemicals
A1386030 |
250 g |
Each for $331.08
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AAA138600B
|
Thermo Scientific Chemicals
A138600B |
1000 g |
Each for $1,012.95
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Description
Prepare 4-phenylurazole from ethyl carbazate and then oxidize the urazole with gaseous dinitrogen tetroxide to yield 4-phenyl-1,2,4-tri- azoline-3,5-dione la. Modification of the ethyl carbazate procedure in which analytically pure monoalkylhydrazine hydrochlorides were isolated in greater than 90% yield, starting from a ketone or aldehyde. Treatment of primary amines is with chloroamine or hydroxylamine-0-sulfonic acid and the condensation of a carbonyl compound with ethyl carbazate. The FeCl 3 -catalyzed reaction of ethyl carbazate (2 b) proceeded readily to give β-hydroxyester 3 b in better yield. A new one-pot neat synthesis of some 5-aryl-2,4-dihydro-3H-1,2,4-triazol-3-ones through cyclocondensation of ethyl carbazate with aryl nitriles catalyzed by DMAP as an efficient and basic nucleophilic catalyst is described.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsPrepare 4-phenylurazole from ethyl carbazate and then oxidize the urazole with gaseous dinitrogen tetroxide to yield 4-phenyl-1,2,4-tri- azoline-3,5-dione la. Modification of the ethyl carbazate procedure in which analytically pure monoalkylhydrazine hydrochlorides were isolated in greater than 90% yield, starting from a ketone or aldehyde. Treatment of primary amines is with chloroamine or hydroxylamine-0-sulfonic acid and the condensation of a carbonyl compound with ethyl carbazate. The FeCl 3 -catalyzed reaction of ethyl carbazate (2 b) proceeded readily to give β-hydroxyester 3 b in better yield. A new one-pot neat synthesis of some 5-aryl-2,4-dihydro-3H-1,2,4-triazol-3-ones through cyclocondensation of ethyl carbazate with aryl nitriles catalyzed by DMAP as an efficient and basic nucleophilic catalyst is described.
Solubility
Very soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
Chemical Identifiers
4114-31-2 | |
104.109 | |
VYSYZMNJHYOXGN-UHFFFAOYSA-N | |
20064 | |
CCOC(=O)NN |
C3H8N2O2 | |
MFCD00007595 | |
ethyl carbazate, ethyl hydrazinecarboxylate, ethoxycarbohydrazide, hydrazinecarboxylic acid, ethyl ester, carbethoxyhydrazine, ethylcarbazate, ethyl carbazinate, carboethoxyhydrazine, monocarbethoxyhydrazine, n-carbethoxy hydrazine | |
ethyl N-aminocarbamate |
Specifications
4114-31-2 | |
85°C to 86°C (7 mmHg) | |
C3H8N2O2 | |
50 g | |
878265 | |
ethyl carbazate, ethyl hydrazinecarboxylate, ethoxycarbohydrazide, hydrazinecarboxylic acid, ethyl ester, carbethoxyhydrazine, ethylcarbazate, ethyl carbazinate, carboethoxyhydrazine, monocarbethoxyhydrazine, n-carbethoxy hydrazine | |
VYSYZMNJHYOXGN-UHFFFAOYSA-N | |
ethyl N-aminocarbamate | |
20064 | |
97% |
44°C to 47°C | |
86°C (186°F) | |
MFCD00007595 | |
UN2811 | |
Moisture sensitive | |
Very soluble in water. | |
CCOC(=O)NN | |
104.109 | |
104.11 | |
Ethyl carbazate |
Safety and Handling
GHS H Statement
H300-H315-H319-H335
Fatal if swallowed.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P260-P264b-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P314-P330-P332+P313-P361-P363-P501c
H301+H311-H315-H319-H335-H373
DOTInformation : Transport Hazard Class: 6.1; Packing Group: III; Proper Shipping Name: TOXIC SOLIDS, ORGANIC, N.O.S.
EINECSNumber : 223-903-3
RTECSNumber : FE2545000
TSCA : Yes
Recommended Storage : Ambient temperatures
RUO – Research Use Only