5-Methoxysalicylic acid

From WikiMD's Wellness Encyclopedia

5-Methoxysalicylic acid


5-Methoxysalicylic acid is an organic compound that belongs to the class of phenols. It is a derivative of salicylic acid, with a methoxy group attached to the fifth carbon atom of the benzene ring.

Chemical Structure[edit | edit source]

The chemical structure of 5-Methoxysalicylic acid consists of a six-membered benzene ring, which is substituted by a carboxylic acid group at the second carbon atom and a methoxy group at the fifth carbon atom. The presence of these functional groups gives the compound its unique chemical properties.

Synthesis[edit | edit source]

5-Methoxysalicylic acid can be synthesized through the Friedel-Crafts alkylation of salicylic acid with dimethyl sulfate. This reaction involves the substitution of a hydrogen atom on the benzene ring with a methoxy group.

Properties[edit | edit source]

5-Methoxysalicylic acid is a white crystalline solid at room temperature. It is soluble in water, ethanol, and diethyl ether. The compound exhibits acidic properties due to the presence of the carboxylic acid group.

Applications[edit | edit source]

5-Methoxysalicylic acid is used in the synthesis of various pharmaceuticals and dyes. It is also used as a laboratory reagent in various chemical reactions.

Safety[edit | edit source]

As with all chemicals, 5-Methoxysalicylic acid should be handled with care. It can cause irritation to the skin and eyes, and may be harmful if swallowed or inhaled.

See Also[edit | edit source]

WikiMD
Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD

Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

WikiMD is not a substitute for professional medical advice. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD