4 - Benzyloxyphenol, recognized chemically for its distinct structure, manifests as a fine, white to off - white powder. Under a microscope, the powder's particles are relatively uniform in size, with a granular yet smooth appearance, allowing for easy handling and flow, which is beneficial for its applications in diverse scientific and industrial processes.
This compound emits a faintly aromatic, phenolic odor. Although the smell is not overpowering, it is characteristic enough to help identify the substance. When it comes to solubility, 4 - Benzyloxyphenol shows poor solubility in polar solvents like water. However, it readily dissolves in many organic solvents such as ethanol, and toluene. This solubility profile is crucial in its processing, extraction, and use in various chemical reactions.
| Name | 4-Benzyloxyphenol |
| Appearance | White To Off-white Powder |
| Shipping Method | Air(UPS, FedEx, TNT, EMS) Or Sea |
| Solubility | Soluble In Water |
| Shelf life | 2 Year |
| Purity | 99.5% |
| Storage Temperature | 2-8°C |
| CAS | 103-16-2 |
| Stability | Stable Under Normal Temperatures And Pressures |
1. Protecting Function
The benzyloxy group in 4 - Benzyloxyphenol serves as an excellent protecting group for the phenolic hydroxyl group. Phenolic hydroxyl groups are highly reactive and can easily undergo oxidation, esterification, and other reactions under various conditions. By introducing the benzyloxy protecting group, the reactivity of the phenolic hydroxyl group is masked, preventing it from participating in unwanted side reactions during complex organic synthesis. This allows chemists to selectively carry out reactions at other functional groups on the molecule, increasing the efficiency and selectivity of the synthesis process.
2. Reaction Intermediate Function
4 - Benzyloxyphenol is a key intermediate in organic synthesis. Its phenolic structure and the presence of the benzyloxy group enable it to participate in a variety of chemical reactions. For example, the phenolic hydroxyl group can undergo acylation reactions with acyl chlorides or anhydrides to form esters. The benzyloxy group can also be involved in reactions such as hydrogenolysis, where it can be selectively removed under specific conditions to regenerate the phenolic hydroxyl group. These reaction capabilities make 4 - Benzyloxyphenol a crucial building block for the synthesis of a wide range of organic compounds, including pharmaceuticals, natural products, and other bioactive molecules.
3. Modification and Functionalization Function
In materials science and other fields, 4 - Benzyloxyphenol can be used to modify and functionalize materials. For example, by reacting with polymers or other materials, it can introduce phenolic - containing functional groups into the material structure. These functional groups can improve the material's properties, such as enhancing the thermal stability, mechanical strength, or chemical resistance of polymers. In addition, the phenolic group can participate in further chemical modifications to introduce other functional moieties, enabling the development of materials with specific properties and applications, such as in the preparation of sensors, coatings, and electronic materials.
