CAS 3535-75-9
:4-Aminopyridine 1-oxide
Description:
4-Aminopyridine 1-oxide, with the CAS number 3535-75-9, is an organic compound characterized by its pyridine ring structure substituted with an amino group and an oxide functional group. This compound typically appears as a white to light yellow crystalline solid and is soluble in polar solvents such as water and alcohols. It exhibits basic properties due to the presence of the amino group, which can participate in protonation reactions. 4-Aminopyridine 1-oxide is known for its role as a pharmacological agent, particularly in the field of neuroscience, where it has been studied for its potential to enhance neurotransmission and improve nerve conduction. Additionally, it may exhibit antioxidant properties, making it of interest in various biochemical applications. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 4-Aminopyridine 1-oxide is a compound of significant interest in both research and potential therapeutic contexts.
Formula:C5H6N2O
InChI:InChI=1S/C5H6N2O/c6-5-1-3-7(8)4-2-5/h1-4H,6H2
InChI key:InChIKey=NDMWRWICFFKKDR-UHFFFAOYSA-N
SMILES:NC=1C=CN(=O)=CC1
Synonyms:- 4-Aminopyridine 1-oxide
- 4-Aminopyridine N-oxide
- 4-Pyridinamine, 1-oxide
- 4-Pyrimidinamine 1-oxide
- 4-iminopyridin-1(4H)-ol
- Brn 0107584
- Nsc 351983
- Phillips 1863
- Pyridine, 4-amino-, 1-oxide
- Pyridine, 4-amino-, N-oxide
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Found 5 products.
4-Aminopyridine N-Oxide
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications 4-Aminopyridine N-Oxide (cas# 3535-75-9) is a compound useful in organic synthesis.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>Formula:C5H6N2OColor and Shape:WhiteMolecular weight:110.114-Aminopyridine N-oxide
CAS:<p>4-Aminopyridine N-oxide is a white, crystalline solid that is soluble in water and alcohol. It has a molecular weight of 128.2 and formula weight of 135.2. 4-Aminopyridine N-oxide reacts with acid solutions to produce nitrous acid and ammonia gas. The rate of the reaction depends on the concentration of aminopyridine and aniline, as well as the pH of the solution. The acetylation, diazotisation, and kinetics have also been studied extensively for this compound. Nitrous acid can react with amides to form azulene, which can then react with amines to form a molecule containing nitrogen, oxygen, carbon, hydrogen and one other element or compound from each group (e.g., NHCOCH). This reaction is reversible when solvents are present.br> 4-Aminopyridine N-oxide may be used as a precursor for other organic</p>Formula:C5H6N2OPurity:Min. 95%Color and Shape:Slightly Yellow PowderMolecular weight:110.11 g/molDalfampridine Related Compound A (4-Aminopyridine 1-oxide)
CAS:Compounds containing an unfused pyridine ring in the structure, nesoiFormula:C5H6N2OColor and Shape:White SolidMolecular weight:110.04801





