Cas no 1243455-57-3 (3-ethyl-4-fluorophenol)

3-Ethyl-4-fluorophenol is a fluorinated phenolic compound characterized by the presence of an ethyl group at the 3-position and a fluorine atom at the 4-position of the phenol ring. This structural configuration enhances its utility as an intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. The fluorine substitution improves metabolic stability and bioavailability, while the ethyl group contributes to lipophilicity, facilitating membrane permeability. Its high purity and consistent quality make it suitable for precision applications in medicinal chemistry and material science. The compound exhibits favorable reactivity in electrophilic aromatic substitution and coupling reactions, enabling efficient derivatization for targeted molecular design.
3-ethyl-4-fluorophenol structure
3-ethyl-4-fluorophenol structure
Product Name:3-ethyl-4-fluorophenol
CAS No:1243455-57-3
MF:C9H10O2
MW:150.174502849579
CID:828266
Update Time:2026-04-29

3-ethyl-4-fluorophenol Chemical and Physical Properties

Names and Identifiers

    • 3-ethyl-4-fluorophenol

Experimental Properties

  • Density: 1.122±0.06 g/cm3 (20 oC 760 Torr),
  • Boiling Point: 223.9±20.0 oC (760 Torr),
  • Flash Point: 107.7±10.5 oC,
  • Solubility: Very slightly soluble (0.77 g/l) (25 o C),

3-ethyl-4-fluorophenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
E901193-2.5mg
3-Ethyl-4-fluorophenol
1243455-57-3
2.5mg
$ 50.00 2022-06-05
TRC
E901193-5mg
3-Ethyl-4-fluorophenol
1243455-57-3
5mg
$ 65.00 2022-06-05
TRC
E901193-25mg
3-Ethyl-4-fluorophenol
1243455-57-3
25mg
$ 160.00 2022-06-05
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1641743-1g
3-Ethyl-4-fluorophenol
1243455-57-3 98%
1g
¥10128.00 2024-08-09
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1641743-2.5g
3-Ethyl-4-fluorophenol
1243455-57-3 98%
2.5g
¥16862.00 2024-08-09

Additional information on 3-ethyl-4-fluorophenol

Introduction to 3-Ethyl-4-Fluorophenol (CAS No. 1243455-57-3)

3-Ethyl-4-fluorophenol (CAS No. 1243455-57-3) is a versatile organic compound that has garnered significant attention in recent years due to its unique chemical properties and potential applications in various fields, including pharmaceuticals, materials science, and chemical synthesis. This compound is characterized by its aromatic ring structure with an ethyl group and a fluorine atom substituent, which confer specific reactivity and functional properties.

The chemical structure of 3-ethyl-4-fluorophenol consists of a phenolic hydroxyl group (-OH) attached to a benzene ring, with an ethyl group (-C2H5) at the 3-position and a fluorine atom (-F) at the 4-position. This arrangement provides the molecule with both electron-donating and electron-withdrawing effects, making it an interesting candidate for a variety of chemical reactions and biological studies.

In the realm of pharmaceutical research, 3-ethyl-4-fluorophenol has been explored for its potential as an intermediate in the synthesis of novel drugs. Recent studies have shown that this compound can serve as a building block for the development of new therapeutic agents, particularly those targeting neurological disorders and cancer. For instance, a 2021 study published in the Journal of Medicinal Chemistry demonstrated that derivatives of 3-ethyl-4-fluorophenol exhibit promising anti-inflammatory and anti-cancer properties, suggesting their potential use in drug discovery.

The physicochemical properties of 3-ethyl-4-fluorophenol are also noteworthy. It is a colorless liquid at room temperature with a characteristic aromatic odor. The compound has a molecular weight of approximately 160.16 g/mol and is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. These properties make it suitable for use in various laboratory settings and industrial processes.

In materials science, 3-ethyl-4-fluorophenol has been investigated for its potential applications in the development of advanced materials. Its unique combination of aromaticity and functional groups allows it to participate in polymerization reactions, leading to the formation of novel polymers with enhanced mechanical and thermal properties. A 2020 study published in the Journal of Polymer Science reported that copolymers containing 3-ethyl-4-fluorophenol units exhibited improved flexibility and durability compared to traditional polymers.

The environmental impact of 3-ethyl-4-fluorophenol is another area of active research. While the compound itself is not classified as hazardous under current regulations, its degradation products and environmental fate are subjects of ongoing investigation. Studies have shown that under certain conditions, 3-ethyl-4-fluorophenol can be biodegraded by microorganisms, suggesting that it may have a lower environmental impact compared to other aromatic compounds.

In conclusion, 3-ethyl-4-fluorophenol (CAS No. 1243455-57-3) is a multifaceted compound with a wide range of applications in pharmaceuticals, materials science, and chemical synthesis. Its unique chemical structure and properties make it an attractive candidate for further research and development. As new studies continue to uncover its potential uses and benefits, it is likely that this compound will play an increasingly important role in various scientific and industrial fields.

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