Description

Methyl 2-(3-amino-2,6-difluorophenyl)acetate (CAS No. 361336-80-3) is a high-purity fluorinated aromatic compound with the molecular formula C₉H₉F₂NO₂. This specialized ester is designed for advanced research applications, particularly in pharmaceutical and agrochemical synthesis. Its unique structure, featuring an amino group and fluorine substituents on the phenyl ring, makes it a valuable intermediate for the development of novel bioactive molecules. Our product is rigorously tested to ensure ≥95% purity (HPLC) and is supplied in sealed, light-resistant packaging to maintain stability. Ideal for medicinal chemistry, this compound offers excellent reactivity for further functionalization, including amidation, reduction, or cross-coupling reactions. Storage recommendation: -20°C under inert atmosphere.

Properties

• CAS Number: 361336-80-3
• Complexity: 213
• IUPAC Name: methyl 2-(3-amino-2,6-difluoro-phenyl)acetate
• InChI: InChI=1S/C9H9F2NO2/c1-14-8(13)4-5-6(10)2-3-7(12)9(5)11/h2-3H,4,12H2,1H3
• InChI Key: ROSSYYRWJGVZJB-UHFFFAOYSA-N
• Exact Mass: 201.06013485
• Molecular Formula: C9H9F2NO2
• Molecular Weight: 201.17
• SMILES: COC(=O)CC1=C(C=CC(=C1F)N)F
• Topological: 52.3
• Monoisotopic Mass: 201.06013485
• Synonyms: Methyl 2-(3-amino-2,6-difluorophenyl)acetate, 361336-80-3, DTXSID20450068, DTXCID40400888, methyl 3-amino-2,6-difluorophenylacetate, (3-AMINO-2,6-DIFLUORO-PHENYL)-ACETIC ACID METHYL ESTER, MFCD06658469, BENZENEACETIC ACID, 3-AMINO-2,6-DIFLUORO-, METHYL ESTER, Methyl (3-amino-2,6-difluorophenyl)acetate, 3-Amino-2,6-difluorobenzeneacetic acid methyl ester, SCHEMBL6286616, ROSSYYRWJGVZJB-UHFFFAOYSA-N, CL8809, AKOS015851541, AB25811, CS-W006855, DS-2311, SB36824, SY113238, DB-007639, Methyl2-(3-amino-2,6-difluorophenyl)acetate, (3-Amino-2,6-difluorophenyl)acetic acid methyl ester, Methyl 2-(3-amino-2 pound not6-difluorophenyl)acetate

Application

Methyl 2-(3-amino-2,6-difluorophenyl)acetate serves as a key building block in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of protease inhibitors and kinase modulators. The compound’s difluorophenyl moiety enhances metabolic stability in drug candidates, while the ester group allows for versatile downstream transformations. Researchers utilize this intermediate in structure-activity relationship (SAR) studies to optimize drug potency and selectivity.

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