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经验公式(希尔记法):
C2H8N2 · C2H2O4
化学文摘社编号:
分子量:
150.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3697941
Assay:
≥96.0% (T)
产品名称
乙肼 草酸酯, ≥96.0% (T)
InChI
1S/C2H8N2.C2H2O4/c1-2-4-3;3-1(4)2(5)6/h4H,2-3H2,1H3;(H,3,4)(H,5,6)
SMILES string
CCNN.OC(=O)C(O)=O
InChI key
DUMHBFMURBWDPC-UHFFFAOYSA-N
assay
≥96.0% (T)
impurities
~2% hydrazine
mp
170-173 °C (dec.)
functional group
amine
carboxylic acid
hydrazine
Quality Level
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
存储类别
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
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)
A method for the regioselective synthesis of 1-alkyl-1H-indazoles.
Liu HJ, et al.
Tetrahedron, 69(19), 3907-3912 (2013)
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
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