Description

Methyl 2-amino-4,6-dichloronicotinate (CAS No. 1044872-40-3) is a high-purity chemical compound with the molecular formula C₇H₆Cl₂N₂O₂. This compound, also known by its IUPAC name methyl 2-amino-4,6-dichloropyridine-3-carboxylate, is a versatile intermediate in organic synthesis and pharmaceutical research. It features a dichlorinated pyridine core with an amino and ester functional group, making it a valuable building block for heterocyclic chemistry applications. Our product is rigorously tested to ensure ≥95% purity (HPLC) and is supplied as a fine white to off-white crystalline powder. Suitable for research and development purposes, it is packaged under inert conditions to guarantee stability and long shelf life. Available in quantities ranging from milligrams to kilograms to meet both lab-scale and bulk requirements.

Properties

• CAS Number: 1044872-40-3
• Complexity: 203
• IUPAC Name: methyl 2-amino-4,6-dichloro-pyridine-3-carboxylate
• InChI: InChI=1S/C7H6Cl2N2O2/c1-13-7(12)5-3(8)2-4(9)11-6(5)10/h2H,1H3,(H2,10,11)
• InChI Key: HJZKXHRUERDKKA-UHFFFAOYSA-N
• Exact Mass: 219.9806328
• Molecular Formula: C7H6Cl2N2O2
• Molecular Weight: 221.04
• SMILES: COC(=O)C1=C(N=C(C=C1Cl)Cl)N
• Topological: 65.2
• Monoisotopic Mass: 219.9806328
• Synonyms: methyl 2-amino-4,6-dichloronicotinate, 1044872-40-3, Methyl 2-amino-4,6-dichloropyridine-3-carboxylate, 2-Amino-4,6-dichloro-nicotinic acid methyl ester, MFCD16660199, Methyl 2-Amino-4,6-dichloro-nicotinate, Methyl2-amino-4,6-dichloronicotinate, SCHEMBL145259, DTXSID90676773, HJZKXHRUERDKKA-UHFFFAOYSA-N, AKOS015891735, CS-W022799, SB80141, AC-22322, DS-11952, FM146286, SY101929, DB-024738, EN300-2008361, methyl 2-amino-4.6-dichloropyridine-3-carboxylate

Application

Methyl 2-amino-4,6-dichloronicotinate serves as a key intermediate in the synthesis of agrochemicals, pharmaceuticals, and specialty chemicals. Its reactive sites enable further functionalization, making it useful in the development of pyridine-based drug candidates. Researchers utilize this compound in cross-coupling reactions, nucleophilic substitutions, and as a precursor for fused heterocycles. It is particularly valuable in medicinal chemistry for constructing bioactive molecules targeting various therapeutic areas.

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