2 4-Difluoroanisole CAS 452-10-8

1. Acts as a key intermediate for synthesizing fluorinated pharmaceutical compounds targeting inflammatory diseases.
2. Serves 2 4-Difluoroanisole CAS 452-10-8 as a core building block for manufacturing selective agrochemicals including herbicides and fungicides.
3. Functions as a reagent for preparing methoxy-substituted aromatic derivatives in fine organic synthesis.
4. Serves 2 4-Difluoroanisole CAS 452-10-8 as a precursor for producing specialty materials used in optoelectronic device manufacturing.

1. Store in sealed amber glass containers at 10–25℃ in a cool, well-ventilated storage area.
2. Keep 2 4-Difluoroanisole CAS 452-10-8 the chemical away from heat, open flames, sparks and other potential ignition sources.
3. Wear chemical-resistant gloves, safety goggles and a vapor respirator during all handling processes.
4. Avoid 2 4-Difluoroanisole CAS 452-10-8 mixing with strong oxidants, strong acids and Lewis acids; dispose of waste via licensed handlers.

1. Features 2,4-disubstituted fluoro groups that enhance the bioactivity of target pharmaceutical products.
2. Provides 2 4-Difluoroanisole CAS 452-10-8 a stable methoxy group for further functionalization reactions like demethylation and substitution.
3. Exhibits excellent solubility in non-protic organic solvents, ensuring homogeneous reaction systems.
4. Delivers 2 4-Difluoroanisole CAS 452-10-8 consistent chemical reactivity suitable for both lab-scale and industrial-scale synthesis.

2 4-Difluoroanisole CAS 452-10-8 is classified as a Class 3 flammable liquid (H226), and its vapors can form explosive mixtures with air. It is irritating to the skin (H315), eyes (H319) and respiratory tract (H335), causing redness, tearing or coughing upon contact or inhalation. It is incompatible with strong oxidants, strong acids and Lewis acids; improper mixing may trigger decomposition and release of irritating fumes. The UN transport number is 1993, and it requires Group III hazardous packaging for transportation.