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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Diphenylmethanes

Comprehensive Overview of (4-Fluorophenyl)-phenyl-methanamine (CAS No. 55095-26-6): Properties, Applications, and Industry Insights

(4-Fluorophenyl)-phenyl-methanamine (CAS No. 55095-26-6) is a fluorinated aromatic amine compound that has garnered significant attention in pharmaceutical and chemical research due to its unique structural properties. The presence of a fluorine substituent on the phenyl ring enhances its electronic characteristics, making it a valuable intermediate in organic synthesis. Researchers and industry professionals often search for terms like "fluorinated aromatic amines applications" or "55095-26-6 synthesis methods", reflecting the growing interest in this compound's versatility.

The molecular structure of (4-fluorophenyl)-phenyl-methanamine combines a phenylmethanamine backbone with a 4-fluorophenyl group, which contributes to its stability and reactivity. This structural feature is particularly relevant in the design of bioactive molecules, as highlighted by recent studies on fluorinated drug intermediates. The compound's CAS registry number, 55095-26-6, serves as a critical identifier in regulatory and safety documentation, ensuring precise communication across global supply chains.

In the context of current industry trends, (4-fluorophenyl)-phenyl-methanamine aligns with the demand for high-performance chemical intermediates in agrochemicals and pharmaceuticals. Searches for "fluorine in medicinal chemistry" or "aromatic amines in drug discovery" underscore its relevance. The compound's potential as a building block for PET imaging agents or small-molecule therapeutics further amplifies its appeal in cutting-edge research.

From a synthetic chemistry perspective, the introduction of fluorine into organic frameworks—often referred to as "fluorination strategies"—has become a hotspot in modern chemistry. (4-Fluorophenyl)-phenyl-methanamine exemplifies this trend, with its synthesis involving selective amine protection and cross-coupling reactions. Researchers frequently explore "CAS 55095-26-6 purity standards" or "scalable synthesis of fluorinated amines" to optimize production processes.

Quality control and analytical characterization of 55095-26-6 are critical for ensuring reproducibility in downstream applications. Techniques such as HPLC, NMR spectroscopy, and mass spectrometry are routinely employed to verify the compound's identity and purity. These methods address common queries like "how to analyze fluorinated aromatic amines" or "55095-26-6 spectroscopic data", which are frequently encountered in academic and industrial forums.

Environmental and regulatory considerations also play a pivotal role in the use of (4-fluorophenyl)-phenyl-methanamine. With increasing focus on green chemistry and sustainable synthesis, efforts to minimize waste and improve atom economy in its production are gaining traction. Searches related to "eco-friendly fluorination techniques" or "REACH compliance for aromatic amines" reflect these evolving priorities.

In summary, (4-Fluorophenyl)-phenyl-methanamine (CAS No. 55095-26-6) represents a compelling case study in the intersection of fluorine chemistry and functional material design. Its applications span pharmaceuticals, agrochemicals, and advanced materials, driven by the persistent demand for high-value chemical intermediates. As research continues to uncover new uses for this compound, its role in innovation remains firmly established.

• 321318-29-0(1-(3,5-Difluorophenyl)ethanamine)
• 66399-30-2((1S)-1-(4-fluorophenyl)ethan-1-amine)
• 321429-49-6((1R)-1-(3-fluorophenyl)ethanamine;hydrochloride)
• 444643-09-8((S)-1-(3-Fluorophenyl)ethanamine)
• 403-40-7(1-(4-Fluorophenyl)ethanamine)
• 444643-16-7((αS)-3,5-Difluoro-α-methylbenzenemethanamine)
• 321318-42-7((R)-1-(4-Fluorophenyl)ethanamine Hydrochloride)
• 321429-48-5((1S)-1-(3-fluorophenyl)ethanamine;hydrochloride)
• 374898-01-8((R)-1-(4-Fluorophenyl)ethanamine)
• 761390-58-3((R)-1-(3-Fluorophenyl)ethanamine)