Acetamide Oxime - CAS 22059-22-9
Catalog: |
BB017327 |
Product Name: |
Acetamide Oxime |
CAS: |
22059-22-9 |
Synonyms: |
N'-hydroxyethanimidamide; N'-hydroxyethanimidamide |
IUPAC Name: | N'-hydroxyethanimidamide |
Description: | Acetamide Oxime (CAS# 22059-22-9) is a useful research chemical. |
Molecular Weight: | 74.08 |
Molecular Formula: | C2H6N2O |
Canonical SMILES: | CC(=NO)N |
InChI: | InChI=1S/C2H6N2O/c1-2(3)4-5/h5H,1H3,(H2,3,4) |
InChI Key: | AEXITZJSLGALNH-UHFFFAOYSA-N |
Boiling Point: | 197.9 °C at 760 mmHg |
Density: | 1.19 g/cm3 |
LogP: | 0.45300 |
GHS Hazard Statement: | H302 (93.02%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
US-2011275801-A1 | Heteroaryl-cyclohexyl-tetraazabenzo[e]azulenes | 20100510 |
US-2011263613-A1 | Compounds and compositions for cognition-enhancement, methods of making, and methods of treating | 20100111 |
US-2011301161-A1 | Benzimidazole inhibitors of leukotriene production | 20091204 |
US-2011034469-A1 | Heterocyclic Compound | 20090804 |
US-2010305086-A1 | Pharmaceutical Compositions for the Treatment of Pain | 20090529 |
PMID | Publication Date | Title | Journal |
22519538 | 20120601 | Studies of histidine residues in soybean (Glycine max) urease | Protein and peptide letters |
22405591 | 20120501 | The physiological implications of urease inhibitors on N metabolism during germination of Pisum sativum and Spinacea oleracea seeds | Journal of plant physiology |
21708099 | 20110901 | Allosteric effects of sulfonate anions on the rates of iron release from serum transferrin | Journal of inorganic biochemistry |
21489785 | 20110601 | An improved bioprocess for synthesis of acetohydroxamic acid using DTT (dithiothreitol) treated resting cells of Bacillus sp. APB-6 | Bioresource technology |
21425838 | 20110414 | One-electron oxidation of acetohydroxamic acid: the intermediacy of nitroxyl and peroxynitrite | The journal of physical chemistry. A |
Complexity: | 49.6 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 1 |
Exact Mass: | 74.048012819 |
Formal Charge: | 0 |
Heavy Atom Count: | 5 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 74.048012819 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 58.6 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | -0.6 |
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