3-Pyridinol, 2-ethyl-6-methyl-


Chemical Name: 3-Pyridinol, 2-ethyl-6-methyl-
CAS Number: 2364-75-2
Product Number: AG002NZY(AGN-PC-0JLJQS)
Synonyms:
MDL No:
Molecular Formula: C8H11NO
Molecular Weight: 137.1790

Identification/Properties


Properties
MP:
169 - 170 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
137.182g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
137.084g/mol
Monoisotopic Mass:
137.084g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
105
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



2-Ethyl-3-hydroxy-6-methylpyridine is a versatile compound that finds extensive application in chemical synthesis. As a multifunctional building block, it is valued for its unique structural properties that enable it to participate in a variety of reactions, leading to the formation of diverse organic compounds. In chemical synthesis, this compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals.Due to its hydroxyl and methyl substituents, 2-Ethyl-3-hydroxy-6-methylpyridine can undergo various chemical transformations, such as oxidation, reduction, alkylation, and acylation reactions. These reactions allow it to be modified and functionalized to tailor its properties for specific applications. Additionally, the heterocyclic nature of the pyridine ring in this compound enhances its reactivity and selectivity in synthetic processes.The presence of the ethyl group provides steric hindrance, which can influence the regioselectivity and stereoselectivity of reactions involving 2-Ethyl-3-hydroxy-6-methylpyridine. This compound can act as a chelating agent due to the hydroxyl group, forming coordination complexes with metal ions and facilitating catalytic processes in organic synthesis.Overall, 2-Ethyl-3-hydroxy-6-methylpyridine plays a crucial role in chemical synthesis by serving as a valuable building block with functional groups that enable a wide range of chemical transformations, making it an essential component in the development of diverse organic compounds.