[A13860] CAS 4114-31-2 | Ethyl carbazate, 97% | Alfa

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Brand: Alfa Aesar

4114-31-2 | C3H8N2O2 | hydrazinecarboxylic acid, ethyl ester

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Chemical Identifiers

CAS
4114-31-2
Molecular Weight (g/mol)
104.11
Synonym
hydrazinecarboxylic acid, ethyl ester
SMILES
CCOC(=O)NN
InChI Key
VYSYZMNJHYOXGN-UHFFFAOYSA-N
Molecular Formula
C3H8N2O2
IUPAC Name
ethoxycarbohydrazide

Specifications

Appearance (Color)
White to pink
Identification (FTIR)
Conforms
Form
Crystals or powder or crystalline powder or lumps or chunks or fused solid
Melting Point (clear melt)
41.0-50.0?C
Assay (GC)
≥96.0%

설명

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.

Applications
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.

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.

Other References:

UN Number:UN2811Beilstein:878265

GHS Hazard and Precautionary Statements

Hazard Statements:H301+H311-H315-H319-H335-H373
GHS H StatementH300-H315-H319-H335Fatal if swallowed.Causes skin irritation.Causes serious eye irritation.May cause respiratory irritation.
Precautionary Statements:P260-P264b-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P314-P330-P332+P313-P361-P363-P501c

Risk & Safety

TSCA:YesRTECS Number:FE2545000

경고:RUO – Research Use Only

CAS4114-31-2FORMULAC3H8N2O2HAZARD CLASS6.1EINECS223-903-3MDLMFCD00007595PACKAGING GROUPIII

Pakage

1000g, 250g, 50G

brand

Alfa Aesar

SKU: A13860 Category:  Brand:
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[A13860] CAS 4114-31-2 | Ethyl carbazate, 97% | Alfa

[A13860] CAS 4114-31-2 | Ethyl carbazate, 97% | Alfa

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