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128279

Sigma-Aldrich

Ethyl hydrazinoacetate hydrochloride

97%

Synonym(s):

(Carbethoxymethyl)hydrazine hydrochloride

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About This Item

Linear Formula:
H2NNHCH2CO2C2H5 · HCl
CAS Number:
Molecular Weight:
154.60
Beilstein/REAXYS Number:
3912112
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

powder

mp

152-154 °C (lit.)

functional group

amine

SMILES string

Cl[H].CCOC(=O)CNN

InChI

1S/C4H10N2O2.ClH/c1-2-8-4(7)3-6-5;/h6H,2-3,5H2,1H3;1H

InChI key

HZZRIIPYFPIKHR-UHFFFAOYSA-N

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Application

Ethyl hydrazinoacetate hydrochloride has been used in the preparation of three novel copper(II) complexes as condensation derivatives of 2-pyridinecarboxaldehyde, 2-acetylpyridine and 2-quinolinecarboxaldehyde.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Nenad Filipović et al.
Chemical biology & drug design, 84(3), 333-341 (2014-03-19)
Novel Pd(II) complex with N-heteroaromatic Schiff base ligand, derived from 8-quinolinecarboxaldehyde (q8a) and ethyl hydrazinoacetate (haOEt), was synthesized and characterized by analytical and spectroscopy methods. The structure of novel complex, as well as structures of its quinoline and pyridine analogues
Copper (II) complexes of N heteroaromatic hydrazones: Synthesis, X-ray structure, magnetic behavior, and antibacterial activity.
Inorgorganica Chimica Acta, 362(6), 1996-2000 (2009)

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