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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:
3912112
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

powder

mp

152-154 °C (lit.)

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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