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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:
6629-60-3
Molecular Weight:
150.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329747878
MDL number:
MFCD00043287
Beilstein/REAXYS Number:
3697941
Assay:
≥96.0% (T)
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Quality Level

200

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

Related Categories

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCG2554
BCBT9376

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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)
Regioselective synthesis of 4-(2-alkyl-5-methyl-2H-pyrazol-3-yl)-piperidines.
Dirat O, et al.
Tetrahedron Letters, 47(11), 1729-1731 (2016)
Giorgio Ramadori et al.
Cell reports, 30(11), 3851-3863 (2020-03-19)
Cancer therapy is limited, in part, by lack of specificity. Thus, identifying molecules that are selectively expressed by, and relevant for, cancer cells is of paramount medical importance. Here, we show that peptidyl-prolyl-cis-trans-isomerase (PPIase) FK506-binding protein 10 (FKBP10)-positive cells are
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
04100-5G04061832097558
04100-25G04061838629043

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