Description

Methyl 5-fluoropyridine-2-carboxylate (CAS No. 107504-07-4) is a high-purity fluorinated pyridine derivative with the molecular formula C₇H₆FNO₂. This compound is a valuable intermediate in pharmaceutical and agrochemical synthesis, offering exceptional reactivity due to its electron-withdrawing fluorine substituent and ester functionality. Its crystalline form ensures consistent batch-to-batch performance, with purity typically exceeding 98% (HPLC). Ideal for nucleophilic substitution, cross-coupling, and hydrolysis reactions, this reagent is packaged under inert gas to maintain stability. Available in quantities from 1g to 1kg, it includes comprehensive NMR, MS, and HPLC analytical data for quality assurance.

Properties

• CAS Number: 107504-07-4
• Complexity: 151
• IUPAC Name: methyl 5-fluoropyridine-2-carboxylate
• InChI: InChI=1S/C7H6FNO2/c1-11-7(10)6-3-2-5(8)4-9-6/h2-4H,1H3
• InChI Key: KCMBKUFSDZMQEM-UHFFFAOYSA-N
• Exact Mass: 155.03825660
• Molecular Formula: C7H6FNO2
• Molecular Weight: 155.13
• SMILES: COC(=O)C1=NC=C(C=C1)F
• Topological: 39.2
• Monoisotopic Mass: 155.03825660
• Synonyms: 107504-07-4, Methyl 5-Fluoropyridine-2-carboxylate, DTXSID00630088, DTXCID90580841, 813-296-9, Methyl 5-fluoropicolinate, MFCD11845630, 2-Pyridinecarboxylicacid,5-fluoro-,methylester(9ci), 2-Pyridinecarboxylic acid, 5-fluoro-, methyl ester, Methyl5-fluoropicolinate, 5-fluoro-pyridine-2-carboxylic acid methyl ester, SCHEMBL424744, SCHEMBL20969977, KCMBKUFSDZMQEM-UHFFFAOYSA-N, BBL103209, STL557019, AKOS006344034, SB13519, SY096916, TS-02065, DB-083253, CS-0018830, 2-Pyridinecarboxylicacid,5-fluoro-,methylester

Application

Methyl 5-fluoropyridine-2-carboxylate serves as a key building block in the synthesis of fluorinated pharmaceuticals, particularly kinase inhibitors and antiviral agents. Its ester group enables facile derivatization into amides or acids, while the fluorine enhances metabolic stability in drug candidates. Researchers also utilize it in material science for constructing fluorinated ligands in catalysis. Strictly for laboratory use under controlled conditions.

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