3-(Prop-2-yn-1-yloxy)phenol, also known by its CAS number 3692-88-4, is an organic compound characterized by its phenolic structure, which includes a hydroxyl group (-OH) attached to a benzene ring. The compound features a prop-2-yn-1-yloxy group, indicating the presence of an alkyne functional group linked through an ether bond to the phenolic moiety. This structure imparts unique chemical properties, including potential reactivity in various organic synthesis reactions, such as nucleophilic substitutions or coupling reactions. The presence of the alkyne group may also allow for further functionalization, making it a valuable intermediate in the synthesis of more complex organic molecules. Additionally, the compound may exhibit specific physical properties such as solubility in organic solvents and varying melting or boiling points, depending on the molecular interactions. Its applications could span across fields such as pharmaceuticals, materials science, and organic chemistry, where it may serve as a building block for more complex compounds or as a reagent in chemical reactions.

3-(prop-2-yn-1-yloxy)phenol

3692-88-4: 3-(Prop-2-yn-1-yloxy)phenol, also known by its CAS number 3692-88-4, is an organic compound characterized by its phenolic structure, which includes a hydroxyl group (-OH) attached to a benzene ring. The compound features a prop-2-yn-1-yloxy group, indicating the presence of an alkyne functional group linked through an ether bond to the phenolic moiety. This structure imparts unique chemical properties, including potential reactivity in various organic synthesis reactions, such as nucleophilic substitutions or coupling reactions. The presence of the alkyne group may also allow for further functionalization, making it a valuable intermediate in the synthesis of more complex organic molecules. Additionally, the compound may exhibit specific physical properties such as solubility in organic solvents and varying melting or boiling points, depending on the molecular interactions. Its applications could span across fields such as pharmaceuticals, materials science, and organic chemistry, where it may serve as a building block for more complex compounds or as a reagent in chemical reactions.

<p>3-(Prop-2-yn-1-yloxy)phenol is a low molecular weight, azide-containing compound. It is synthesized by the reaction of propargyl alcohol with sodium azide in the presence of magnesium as a catalyst. 3-(Prop-2-yn-1-yloxy)phenol can be used as an activating agent for Grignard reagents, and it has been shown to be effective in bulk polymerization reactions. The terminal alkynes react with 1,3-dipolar cycloaddition to form two new carbon atoms that are bound to the original carbon atom. This process is known as transfer. 3-(Prop-2-yn-1-yloxy)phenol has also been shown to have low molecular weight, which makes it useful for reactions at lower temperatures.</p>

CAS 3692-88-4

3-(prop-2-yn-1-yloxy)phenol

3-(Prop-2-yn-1-yloxy)phenol

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