| Weight | 74.083 g/mol |
|---|---|
| Formula | C2H6N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Acethydrazide (1068-57-1)
acetylhydrazine · acetylhydrazide · acetylhydrazine monohydrochloride
Score:
#1818 in Biochemistry
,
#4977 in Chemistry
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- Antituberculosis agentsI : -[5-(2-Furyl)-1,2,4-triazol-3-ylthio] acethydrazide and related compounds (Tetrahedron, 1970)
- Spin-trapping of free radicals formed during microsomal metabolism of ethylhydrazine and acetylhydrazine (Biochemical and Biophysical Research Communications, 1981)
- Acetylhydrazine hepatotoxicity*1 (Toxicology and Applied Pharmacology, 1981)
- The Apparent Ionization Constants of Acethydrazide and Glycylhydrazide (Journal of the American Chemical Society, 1949)
- Hepatic gene expression and lipid homeostasis in C57BL/6 mice exposed to hydrazine or acetylhydrazine (Toxicological Sciences, 2004)
- Factors affecting the metabolism of [14C]acetylhydrazine in rats. (Drug Metabolism and Disposition, 1978)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - acetylhydrazine
- acetylhydrazide
- acetylhydrazine monohydrochloride
- acetylhydrazine, (E)-2-fumarate (1:1)
- acethydrazine
- monoacetylhydrazine
- acetohydrazide
-
SMILESCC(=O)NN
-
InChIKeyOFLXLNCGODUUOT-UHFFFAOYSA-N
- Pubchem - Acethydrazide
- Wikipedia - acetylhydrazine
Acylhydrazines are a class of organic compounds and can be regarded as nitrogen derivatives of carboxylic acids having the general structure R-CO-NR1-NR2R3, where R1, R2 and R3 can be organic radicals or hydrogen. They are analogous to an amide, but the -OH portion of a carboxylic acid is replaced by hydrazine rather than ammonia (one less hydrogen at the point of attachment). Acylhydrazines are a type of hydrazides.
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Acethydrazide
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