128279
肼基乙酸乙酯 盐酸盐
97%
别名:
(Carbethoxymethyl)hydrazine hydrochloride
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关于此项目
线性分子式:
H2NNHCH2CO2C2H5 · HCl
化学文摘社编号:
分子量:
154.60
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
230-104-3
Beilstein/REAXYS Number:
3912112
MDL number:
Assay:
97%
Form:
powder
产品名称
肼基乙酸乙酯 盐酸盐, 97%
InChI key
HZZRIIPYFPIKHR-UHFFFAOYSA-N
InChI
1S/C4H10N2O2.ClH/c1-2-8-4(7)3-6-5;/h6H,2-3,5H2,1H3;1H
SMILES string
Cl[H].CCOC(=O)CNN
assay
97%
form
powder
mp
152-154 °C (lit.)
functional group
amine
ester
hydrazine
Quality Level
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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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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