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Merck
CN

04100

Ethylhydrazine oxalate

≥96.0% (T)

Synonym(s):

Ethylhydrazine ethanedioate

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About This Item

Empirical Formula (Hill Notation):
C2H8N2 · C2H2O4
CAS Number:
Molecular Weight:
150.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3697941
Assay:
≥96.0% (T)
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Quality Level

assay

≥96.0% (T)

impurities

~2% hydrazine

mp

170-173 °C (dec.)

functional group

amine, carboxylic acid, hydrazine

SMILES string

CCNN.OC(=O)C(O)=O

InChI

1S/C2H8N2.C2H2O4/c1-2-4-3;3-1(4)2(5)6/h4H,2-3H2,1H3;(H,3,4)(H,5,6)

InChI key

DUMHBFMURBWDPC-UHFFFAOYSA-N

Application

Ethylhydrazine oxalate can be used to synthesize:
  • 1-ethyl-1H-indazoles
  • 3-substituted 1-ethyl-6-methylpyrimido[4,5-c]pyridazine-5,7(1H,6H)-dione derivatives
  • 4-(2-alkyl-5-methyl-2H-pyrazol-3-yl)-piperidines



signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 1B - Skin Sens. 1

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



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Regioselective synthesis of 4-(2-alkyl-5-methyl-2H-pyrazol-3-yl)-piperidines.
Dirat O, et al.
Tetrahedron Letters, 47(11), 1729-1731 (2016)
Parallel Synthesis of Novel 3-Substituted 1-Ethyl-6-methylpyrimido [4, 5-c] pyridazine-5, 7 (1 H, 6 H)-dione Analogs.
Chen Y, et al.
Synthetic Communications, 40(6), 821-832 (2010)
A method for the regioselective synthesis of 1-alkyl-1H-indazoles.
Liu HJ, et al.
Tetrahedron, 69(19), 3907-3912 (2013)



Global Trade Item Number

SKUGTIN
D171301-25G04061831826463
04100-25G04061838629043
04100-5G04061832097558