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

Comprehensive Guide to 2-4-(Ethoxycarbonyl)-3-fluorophenylphenol (CAS No. 1261975-80-7): Properties, Applications, and Market Insights

2-4-(Ethoxycarbonyl)-3-fluorophenylphenol (CAS No. 1261975-80-7) is a specialized organic compound gaining attention in pharmaceutical and agrochemical research. This fluorinated phenolic derivative features a unique molecular structure combining an ethoxycarbonyl group and fluorophenyl moiety, making it valuable for various synthetic applications. Researchers particularly value its role as a building block in drug discovery and material science.

The compound's chemical properties include moderate solubility in organic solvents like DMSO and ethanol, with limited water solubility. Its molecular weight of 274.28 g/mol and specific fluorine substitution pattern contribute to its reactivity profile. The presence of both phenolic OH and ester functionalities allows for diverse chemical modifications, making 2-4-(Ethoxycarbonyl)-3-fluorophenylphenol a versatile intermediate in organic synthesis.

Recent studies highlight the compound's potential in developing new-generation pharmaceuticals, particularly in areas addressing current global health challenges. Its structural features show promise for creating targeted therapies with improved efficacy and reduced side effects. The fluorine atom in the molecule enhances metabolic stability, a property highly sought after in modern drug design.

In material science applications, 2-4-(Ethoxycarbonyl)-3-fluorophenylphenol serves as a precursor for advanced polymers with unique thermal and optical properties. Researchers are exploring its use in developing specialty coatings and electronic materials, responding to growing demands in renewable energy and sustainable technology sectors.

The global market for fluorinated fine chemicals like 2-4-(Ethoxycarbonyl)-3-fluorophenylphenol is experiencing steady growth, driven by pharmaceutical innovation and material science advancements. Current market analysis suggests increasing demand from research institutions and specialty chemical manufacturers, particularly in North America and Asia-Pacific regions.

Quality control measures for CAS 1261975-80-7 typically involve HPLC analysis with UV detection, ensuring high purity levels (>98%) required for research applications. Proper storage conditions recommend protection from moisture and light at controlled temperatures to maintain stability.

Environmental and safety considerations for handling 2-4-(Ethoxycarbonyl)-3-fluorophenylphenol follow standard laboratory protocols for organic compounds. While not classified as hazardous under current regulations, appropriate personal protective equipment is recommended during handling, reflecting the growing emphasis on laboratory safety standards in chemical research.

Future research directions for this compound include exploring its potential in green chemistry applications and developing more efficient synthetic routes. The compound's unique structure positions it as a candidate for catalysis research and bioconjugation chemistry, addressing current scientific challenges in these fields.

For researchers seeking high-purity 2-4-(Ethoxycarbonyl)-3-fluorophenylphenol, several specialty chemical suppliers offer the compound in various quantities. The current pricing reflects its status as a research-grade chemical, with costs varying based on purity levels and order volume.

Recent patent literature reveals growing interest in 1261975-80-7 derivatives for various applications, particularly in medicinal chemistry. This trend aligns with the pharmaceutical industry's focus on fluorinated compounds as privileged structures in drug development.

Analytical characterization of 2-4-(Ethoxycarbonyl)-3-fluorophenylphenol typically includes NMR spectroscopy (1H and 13C), mass spectrometry, and IR spectroscopy. These techniques confirm structural identity and purity, essential for research applications where precise molecular characteristics are crucial.

The synthesis of CAS 1261975-80-7 generally involves multi-step organic reactions starting from commercially available fluorinated precursors. Recent improvements in synthetic methodologies have enhanced yields and reduced environmental impact, responding to the chemical industry's push toward sustainable synthesis practices.

In formulation development, the ethoxycarbonyl-fluorophenylphenol structure offers interesting possibilities due to its balanced lipophilicity and hydrogen bonding capacity. These properties make it valuable for optimizing drug delivery systems and improving bioavailability in pharmaceutical applications.

Regulatory status of 2-4-(Ethoxycarbonyl)-3-fluorophenylphenol varies by region, but it generally falls under standard laboratory chemical classifications. Researchers should consult local regulations when planning studies involving this compound, especially considering increasing global attention to chemical safety assessment protocols.

Emerging applications for this compound include its use in molecular imaging probes and diagnostic agents, leveraging its fluorine atom for potential PET imaging applications. This aligns with current medical research trends toward precision medicine and theranostic approaches.

For those working with 1261975-80-7, proper documentation of experimental procedures and results is essential. The scientific community benefits from shared data on this compound's behavior in various reactions, contributing to the collective knowledge of fluorinated building blocks in synthetic chemistry.

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