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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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Copper (II) complexes of N heteroaromatic hydrazones: Synthesis, X-ray structure, magnetic behavior, and antibacterial activity.
Inorgorganica Chimica Acta, 362(6), 1996-2000 (2009)
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

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