Key Properties and Applications of 4-(Trifluoromethoxy)benzyl Alcohol
In the realm of chemical synthesis and material science, specific intermediates play a pivotal role in enabling innovation. 4-(Trifluoromethoxy)benzyl Alcohol, identified by CAS number 1736-74-9, is one such compound, valued for its unique trifluoromethoxy group and its utility as a versatile building block. For professionals in R&D, formulation, and procurement, understanding its properties and applications is key to leveraging its full potential.
Chemical Profile of 4-(Trifluoromethoxy)benzyl Alcohol
This organic compound, with the molecular formula C8H7F3O2 and a molecular weight of 192.135, is a derivative of benzyl alcohol. Its key characteristics include:
- Purity: Typically offered at a minimum purity of 97%, ensuring reliability in sensitive chemical processes.
- Physical State: Commonly found as a clear, colorless oil.
- Boiling Point: Approximately 203.4±35.0 °C at 760 mmHg, indicating its thermal stability under moderate conditions.
- Density: Around 1.3±0.1 g/cm³, a standard parameter for chemical identification and formulation.
- Solubility: Soluble in common organic solvents like methanol and chloroform, facilitating its use in various reaction media.
The trifluoromethoxy (-OCF3) group imparts distinct electronic and lipophilic properties, making this benzyl alcohol derivative a valuable moiety in the design of new molecules.
Applications in Chemical and Pharmaceutical Industries
The versatility of 4-(Trifluoromethoxy)benzyl Alcohol makes it indispensable in several sectors:
- Pharmaceutical Intermediates: Its structure serves as a foundational element for synthesizing active pharmaceutical ingredients (APIs). The trifluoromethoxy group can enhance metabolic stability, lipophilicity, and binding affinity of drug candidates, making it a sought-after component in medicinal chemistry. Researchers actively seek suppliers to buy this compound for drug discovery pipelines.
- Organic Synthesis: As a functionalized benzyl alcohol, it participates in a wide array of organic reactions, including esterification, etherification, oxidation, and nucleophilic substitutions. It acts as a key building block for constructing more complex organic molecules used in agrochemicals, dyes, and specialty polymers.
- Material Science: The unique properties conferred by the fluorinated group can also be beneficial in developing advanced materials, such as functional polymers or electronic chemicals.
Procuring 4-(Trifluoromethoxy)benzyl Alcohol from China
For industries requiring a consistent and high-quality supply of 4-(Trifluoromethoxy)benzyl Alcohol (CAS 1736-74-9), partnering with established Chinese manufacturers like NINGBO INNO PHARMCHEM CO.,LTD is a strategic choice. They offer competitive pricing and ensure product integrity through professional packaging and reliable logistics, enabling seamless procurement for global R&D and manufacturing operations. If you are looking to purchase this chemical intermediate, engaging with a trusted manufacturer will guarantee product quality and supply chain stability.
Perspectives & Insights
Nano Explorer 01
“Organic Synthesis: As a functionalized benzyl alcohol, it participates in a wide array of organic reactions, including esterification, etherification, oxidation, and nucleophilic substitutions.”
Data Catalyst One
“It acts as a key building block for constructing more complex organic molecules used in agrochemicals, dyes, and specialty polymers.”
Chem Thinker Labs
“Material Science: The unique properties conferred by the fluorinated group can also be beneficial in developing advanced materials, such as functional polymers or electronic chemicals.”