3,4-Difluoro-2-methoxyphenylacetic acid (CAS 1558274-26-2) is a specialized phenylacetic acid derivative featuring a distinctive substitution pattern on the aromatic ring. Structurally, 3,4-Difluoro-2-methoxyphenylacetic acid consists of a phenylacetic acid core with a methoxy group at the 2-position and fluorine atoms at the 3- and 4-positions of the benzene ring.
3,4-Difluoro-2-methoxyphenylacetic acid is a key synthetic intermediate and building block in pharmaceutical research and development, particularly valuable for the construction of drug candidates requiring enhanced metabolic stability and lipophilicity. As a fluorinated phenylacetic acid derivative, 3,4-Difluoro-2-methoxyphenylacetic acid enables medicinal chemists to introduce critical physicochemical properties into target molecules. In analytical development contexts, 3,4-Difluoro-2-methoxyphenylacetic acid serves as a reference standard for monitoring synthetic processes. The unique electronic profile of 3,4-Difluoro-2-methoxyphenylacetic acid makes it a valuable tool for structure-activity relationship (SAR) studies exploring the impact of aromatic substitution on biological activity.
Product Parameters
Parameter
Specification
Product Name
3,4-Difluoro-2-methoxyphenylacetic acid
CAS Number
1558274-26-2
Molecular Formula
C₉H₈F₂O₃
Molecular Weight
202.15 g/mol
Appearance
White powder
Boiling Point
286.5 ± 35.0 °C
Density
1.354 ± 0.06 g/cm3
Storage Condition
2–8°C
Application
3,4-Difluoro-2-methoxyphenylacetic acid is an important fluorinated phenylacetic acid derivative that can serve as a key intermediate in inhibiting overactive or overexpressed signal transduction pathways in cancer tissues.
Product Advantages
Strategic Fluorination for Drug Optimization
3,4-Difluoro-2-methoxyphenylacetic acid provides a strategic fluorination pattern that enhances metabolic stability and lipophilicity — key considerations in modern drug design.
Versatile Synthetic Building Block
3,4-Difluoro-2-methoxyphenylacetic acid offers multiple functional handles for chemical derivatization, enabling the synthesis of diverse compound libraries through amidation, esterification, and other common transformations.
Electronic Property Tuning
The electron-withdrawing fluorine atoms at the 3- and 4-positions significantly alter the electronic properties of the aromatic ring, providing a distinct profile compared to non-fluorinated or singly fluorinated analogs.
High-Purity Reference Standard
Cosperpharm supplies 3,4-Difluoro-2-methoxyphenylacetic acid at ≥97% purity with full characterization data, suitable for medicinal chemistry, process development, and analytical applications.
FAQ
Q1: How should this compound be stored?
A: Store 3,4-Difluoro-2-methoxyphenylacetic acid in a tightly sealed container at 2–8°C or –20°C, protected from light .
Q2: Is 3,4-Difluoro-2-methoxyphenylacetic acid hazardous?
A: 3,4-Difluoro-2-methoxyphenylacetic acid is classified with hazard statements H302 (Harmful if swallowed), H315 (Causes skin irritation), H319 (Causes serious eye irritation), and H335 (May cause respiratory irritation) .
Contact Us
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