CAS 22320-10-1

methyl 4-(4-hydroxyphenyl)butanoate

Description:

Methyl 4-(4-hydroxyphenyl)butanoate, also known as methyl 4-(p-hydroxyphenyl)butanoate, is an organic compound characterized by its ester functional group and a phenolic moiety. It features a butanoate backbone with a hydroxyl group attached to a para-positioned phenyl ring, contributing to its potential biological activity. This compound is typically a colorless to pale yellow liquid with a pleasant odor, indicating its volatility and potential for use in fragrance applications. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic characteristics. Methyl 4-(4-hydroxyphenyl)butanoate may exhibit antioxidant properties, making it of interest in various fields, including pharmaceuticals and cosmetics. Its structure allows for potential interactions with biological systems, which could be explored for therapeutic applications. As with many organic compounds, safety data should be consulted to understand its handling and potential hazards. Overall, this compound represents a unique blend of structural features that may confer specific functional properties in chemical and biological contexts.

Formula: C₁₁H₁₄O₃

InChI: InChI=1/C11H14O3/c1-14-11(13)4-2-3-9-5-7-10(12)8-6-9/h5-8,12H,2-4H2,1H3

SMILES: COC(=O)CCCc1ccc(cc1)O

Synonyms:

• 4-(4-Hydroxyphenyl)butanoic acid methyl ester
• Benzenebutanoic acid, 4-hydroxy-, methyl ester
• Butyric acid, 4-(p-hydroxyphenyl)-, methyl ester

4-​Hydroxy-​benzenebutanoic Acid Methyl Ester

Controlled Product

CAS: 22320-10-1

Applications 4-​Hydroxy-​benzenebutanoic Acid Methyl Ester is an intermediate in synthesizing Arbutamine (A766300). It is a cardiac stimulant. Arbutamine stimulates adrenergic receptors.
References Sinusas, A., et al.: J. Nucl. Med., 35, 664 (1994); Sansoy, V., et al.: Circulation, 92, 994 (1995); Elhendy, A., et al.: Eur. J. Nucl. Med., 23, 1354 (1996);

Formula: C₁₁H₁₄O₃

Color and Shape: Neat

Molecular weight: 194.23

Ref: TR-B185298