Oxazole

From WikiMD's medical encyclopedia

Oxazole is an organic compound with the formula C_3H_3NO. It is a five-membered heterocyclic compound containing an oxygen atom and a nitrogen atom at non-adjacent positions. As one of the azole compounds, oxazole is aromatic, with electron delocalization occurring over the ring, allowing it to exhibit resonance stability. The structure of oxazole is similar to that of imidazole and thiazole, with the oxygen atom replacing the nitrogen or sulfur atom respectively.

Structure and Bonding

Oxazole's aromaticity is derived from the sextet of π-electrons, similar to the aromaticity observed in benzene. The heteroatoms (oxygen and nitrogen) contribute to the ring's electron density through p-orbital overlap, creating a stable, delocalized π-electron system. The presence of heteroatoms also affects the compound's electronic properties, making oxazole a site for potential chemical reactions, particularly at positions 2, 4, and 5 of the ring.

Synthesis

Several methods exist for the synthesis of oxazoles, including the cyclodehydration of amide derivatives and the condensation of aldehydes with amides or ureas in the presence of dehydrating agents. The Robinson-Gabriel synthesis is a well-known procedure for producing oxazoles, involving the cyclization of α-acylamino ketones.

Reactivity and Applications

Oxazoles are known for their reactivity, particularly in electrophilic substitution reactions at the 2 and 4 positions of the ring. They serve as key intermediates in the synthesis of more complex molecules, including pharmaceuticals and agrochemicals. Oxazole derivatives exhibit a wide range of biological activities, making them valuable in drug discovery and medicinal chemistry.

Biological Significance

Compounds containing the oxazole ring are found in a variety of biologically active molecules. For example, oxazolidinones are a class of antibiotics that target bacterial ribosomes to inhibit protein synthesis. Natural products, such as the marine toxin palytoxin, also contain oxazole rings, indicating the structural diversity and biological relevance of this heterocycle.

Safety and Toxicology

The safety and toxicity of oxazole and its derivatives depend on the specific compound and its concentration. While some oxazole derivatives are used in pharmaceuticals, others may be toxic or hazardous. Proper handling, storage, and disposal of these compounds are essential to minimize environmental and health risks.

See Also

References


Chemistry icon li.svg
This article is a stub related to chemistry. You can help WikiMD by expanding it!


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

Transform your life with W8MD's budget GLP-1 injections from $125.

W8mdlogo.png
W8MD weight loss doctors team

W8MD offers a medical weight loss program to lose weight in Philadelphia. Our physician-supervised medical weight loss provides:

NYC weight loss doctor appointments

Start your NYC weight loss journey today at our NYC medical weight loss and Philadelphia medical weight loss clinics.

Linkedin_Shiny_Icon Facebook_Shiny_Icon YouTube_icon_(2011-2013) Google plus


Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD