4hydroxy35dimethoxystyrene

The term "4hydroxy35dime..." appears truncated and does not correspond to a well-established chemical name. A plausible reconstruction is 4-hydroxy-3,5-dimethylphenol, a substituted phenol in which a benzene ring bears two methyl groups at positions 3 and 5 and two hydroxyl groups at positions 1 and 4 (counting the phenolic OH as position 1). The formula for this kind of structure is commonly given as C8H10O2, and it belongs to the class of dihydroxy, dimethyl-substituted phenols.

Chemical identity and structure: As a phenolic compound with two hydroxyl groups, it is more polar than many simple alkylbenzenes and can form hydrogen bonds. The two methyl substituents increase hydrophobic character relative to the parent dihydroxybenzene, giving mixed solubility properties: limited water solubility but appreciable solubility in many organic solvents. The exact physical properties, such as melting and boiling points, depend on isomeric arrangement and purity.

Occurrence and potential uses: This class of compounds is widely studied as intermediates in organic synthesis. Related dihydroxy, dimethylphenols can serve as precursors to dyes, fragrances, and polymer stabilizers, or as building blocks for more complex aromatic molecules.

Synthesis and reactions: Possible routes include selective methylation of a suitable phenol core followed by controlled hydroxylation, or modification of a pre-existing dihydroxyphenol. Phenolic compounds undergo typical reactions such as O-alkylation, ether formation, and oxidative transformations, with reactivity influenced by the two directing hydroxy groups.

Safety: Phenols can be corrosive and irritants. Handle with appropriate PPE, work in a ventilated area, and avoid skin contact. Store away from oxidizers and heat.