Understanding the precise chemical properties of a compound is fundamental to its effective utilization in any field. (4-Vinylphenyl)methanol, bearing the CAS number 1074-61-9, is no exception. This light yellow liquid is a bifunctional organic molecule, featuring a styrene derivative structure with a hydroxymethyl group. Its chemical formula is C9H10O, and it has a molecular weight of approximately 134.18 g/mol. These basic attributes provide a foundation for its reactivity and application as a versatile organic intermediate.

The molecular structure of (4-Vinylphenyl)methanol is key to its chemical behavior. The presence of the vinyl group (CH=CH2) attached to the phenyl ring makes it susceptible to addition reactions, most notably polymerization. This makes it a valuable monomer for creating vinyl-based polymers and copolymers. The vinyl group can also undergo other electrophilic addition reactions. Complementing this is the hydroxymethyl group (-CH2OH), which behaves as a typical primary alcohol. It can be easily oxidized to an aldehyde or carboxylic acid, esterified, or converted into halides or ethers. These reactions allow chemists to further modify the molecule, creating a broader spectrum of derivatives. When considering the price of (4-Vinylphenyl)methanol, these inherent chemical reactivities are significant factors.

The synthesis of (4-Vinylphenyl)methanol commonly involves routes that are well-established in organic chemistry. One prevalent method is the reduction of 4-vinylbenzoic acid or its esters. For instance, using reducing agents like lithium aluminum hydride (LiAlH4) can effectively convert the carboxyl group to a primary alcohol. The process requires careful control of reaction conditions, including temperature and solvent, to maximize yield and purity. Another approach might involve the functionalization of related styrene derivatives. Ensuring a stable supply of this crucial chemical intermediate is vital for many downstream applications.

Purification of (4-Vinylphenyl)methanol after synthesis is often achieved through techniques such as distillation or column chromatography to remove byproducts and unreacted starting materials. Stabilizers, like p-tert-butylcatechol (TBC), are frequently added to prevent spontaneous polymerization of the vinyl group during storage and handling, especially at elevated temperatures. Manufacturers like NINGBO INNO PHARMCHEM CO.,LTD. pay close attention to these details to deliver a reliable product. If you are looking to buy (4-Vinylphenyl)methanol, understanding its synthesis and stabilization practices will help in making an informed decision.

In essence, (4-Vinylphenyl)methanol is a compound of significant chemical interest due to its dual reactive sites. Its well-defined properties and accessible synthesis routes position it as an indispensable organic intermediate for numerous industrial applications. NINGBO INNO PHARMCHEM CO.,LTD. is committed to supplying this high-quality chemical building block to facilitate advancements in various sectors.