Atomfair Pyridine, 2-methoxy-5-methyl- C7H9NO

Description 2-Methoxy-5-methylpyridine (CAS No. 13472-60-1) is a high-purity heterocyclic organic compound with the molecular formula C7H9NO . This specialized chemical is a valuable intermediate in pharmaceutical and agrochemical synthesis, featuring a pyridine core substituted with a methoxy group at the 2-position and a methyl group at the 5-position. Its unique structure makes it a versatile building block for the development of active pharmaceutical ingredients (APIs) and fine chemicals. Our product is rigorously tested to ensure exceptional quality, with ??98% purity (GC), and is supplied in sealed containers under inert gas to maintain stability. Ideal for researchers in medicinal chemistry, catalysis,…

Description

2-Methoxy-5-methylpyridine (CAS No. 13472-60-1) is a high-purity heterocyclic organic compound with the molecular formula C₇H₉NO. This specialized chemical is a valuable intermediate in pharmaceutical and agrochemical synthesis, featuring a pyridine core substituted with a methoxy group at the 2-position and a methyl group at the 5-position. Its unique structure makes it a versatile building block for the development of active pharmaceutical ingredients (APIs) and fine chemicals. Our product is rigorously tested to ensure exceptional quality, with ??98% purity (GC), and is supplied in sealed containers under inert gas to maintain stability. Ideal for researchers in medicinal chemistry, catalysis, and material science, this compound is available in quantities ranging from grams to kilograms to meet both lab-scale and industrial needs.

CAS No: 13472-60-1
Molecular Formula: C7H9NO
Molecular Weight: 123.15
Exact Mass: 123.068413911
Monoisotopic Mass: 123.068413911
IUPAC Name: 2-methoxy-5-methylpyridine
SMILES: CC1=CN=C(C=C1)OC
Synonyms: 2-Methoxy-5-methylpyridine, 13472-56-5, Pyridine, 2-methoxy-5-methyl-, 6-Methoxy-3-picoline, 3-Picoline, 6-methoxy-

Application

2-Methoxy-5-methylpyridine serves as a key synthon in the preparation of pharmaceuticals, particularly in the synthesis of antihypertensive and antiviral agents. It is also employed as a ligand in transition metal-catalyzed reactions due to its electron-donating methoxy group. Additionally, this compound finds use in agrochemical research for the development of novel pesticides and herbicides. Its stability and reactivity make it suitable for functionalization via cross-coupling or nucleophilic substitution reactions.

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