Phenol, 3-(2-propenyl)-, also known as allylphenol, is an organic compound characterized by a phenolic structure with an allyl group attached to the aromatic ring. It is a colorless to pale yellow liquid with a distinctive odor. This compound is soluble in organic solvents and exhibits limited solubility in water due to the hydrophobic nature of the allyl group. Allylphenol is known for its antimicrobial properties and is often used in the synthesis of various chemical intermediates, including fragrances and pharmaceuticals. It can undergo typical electrophilic aromatic substitution reactions, making it a versatile building block in organic synthesis. Additionally, it may participate in polymerization reactions due to the presence of the allyl group, which can lead to the formation of larger, more complex molecules. Safety considerations include its potential irritant effects on skin and mucous membranes, necessitating appropriate handling precautions in laboratory and industrial settings.

Phenol, 3-(2-propenyl)-

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3-(3-Hydroxyphenyl)-1-propene

3-Allylphenol

Phenol, 3-(2-propen-1-yl)-

3-Allylphenol is a methoxy substituted phenolic compound. It is used as a model compound to study the mechanisms of hydrophobic interactions in lignocellulosic biomass. 3-Allylphenol has been shown to have water absorption properties, which may be due to its ability to form hydrogen bonds with water molecules. It also has an affinity for lignin, a polymeric material that makes up the bulk of plant cell walls, and can be converted into bio-oil through thermogravimetric analysis. 3-Allylphenol also undergoes gas phase reactions when heated at high temperatures, leading to the formation of methane and carbon dioxide.

3-Allylphenol is an inhibitor of dopamine β-hydroxylase (DBH; Ki = 12 mM).

CAS 1446-24-8: Phenol, 3-(2-propenyl)-

3-(3-Hydroxyphenyl)-1-propene

Ref: 10-F392626

3-Allylphenol

Ref: 54-OR19551

Phenol, 3-(2-propen-1-yl)-

Ref: IN-DA001JTR

3-Allylphenol

Ref: 3D-BAA44624

3-Allylphenol

Ref: TM-T71942