CAS 10242-36-1
:2-Pyridinemethanol, 1-oxide
Description:
2-Pyridinemethanol, 1-oxide, also known as pyridine-2-methanol N-oxide, is an organic compound characterized by its pyridine ring structure with a hydroxymethyl group and an N-oxide functional group. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its form and purity. It is soluble in polar solvents such as water and alcohols, which is indicative of its polar nature due to the presence of the hydroxymethyl and N-oxide groups. The N-oxide functionality can influence its reactivity, making it a potential candidate for various chemical reactions, including oxidation and nucleophilic substitution. Additionally, 2-Pyridinemethanol, 1-oxide may exhibit biological activity, which could be of interest in medicinal chemistry. Its properties, such as boiling point, melting point, and specific reactivity, can vary based on the conditions and the presence of other functional groups in a given reaction environment. Overall, this compound serves as a useful building block in organic synthesis and pharmaceutical applications.
Formula:C6H7NO2
InChI:InChI=1S/C6H7NO2/c8-5-6-3-1-2-4-7(6)9/h1-4,8H,5H2
InChI key:InChIKey=FNHPXOZSWXLMGI-UHFFFAOYSA-N
SMILES:C(O)C=1N(=O)=CC=CC1
Synonyms:- (1-Oxidopyridin-2-Yl)Methanol
- 2-(Hydroxymethyl)pyridin-1-ium-1-olate
- 2-(Hydroxymethyl)pyridine 1-oxide
- 2-(Hydroxymethyl)pyridine N-oxide
- 2-Picolyl alcohol 1-oxide
- 2-Pyridinemethanol N-oxide
- 2-Pyridinemethanol, 1-oxide
- 2-Pyridylcarbinol N-oxide
- 2-Pyridylmethanol N-oxide
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
2-(Hydroxymethyl)pyridine N-Oxide
CAS:Controlled Product<p>Applications 2-(Hydroxymethyl)pyridine N-Oxide (cas# 10242-36-1) is a compound useful in organic synthesis.<br></p>Formula:C6H7NO2Color and Shape:NeatMolecular weight:125.132-(Hydroxymethyl)pyridine N-oxide
CAS:<p>2-(Hydroxymethyl)pyridine N-oxide is a model system that was originally synthesized to study the mechanism of perchlorate and amine degradation in vivo. It has been shown to be an excellent model for studying the oxidative decomposition of n-oxides with metal ions, as well as their transformation into monomers. 2-(Hydroxymethyl)pyridine N-oxide reacts with chloride ion to form 2-(hydroxymethyl)pyridine N-oxide chloride. The reaction of 2-(hydroxymethyl)pyridine N-oxide with a sulfoxide produces an adduct that can be used to study hydrogen bonding. 2-(Hydroxymethyl)pyridine N-oxide has biological properties and is a potential drug candidate for the treatment of cancer.</p>Formula:C6H7NO2Purity:Min. 95%Molecular weight:125.13 g/mol


