104516-57-6

Basic information

• Product Name: 2-(5-ISOXAZOLYL)-4-METHYLPHENOL
• Synonyms: 2-(5-ISOXAZOLYL)-4-METHYLPHENOL;2-(ISOXAZOL-5-YL)-4-METHYLPHENOL;5-(2'-HYDROXY-5'-METHYLPHENYL)-ISOXAZOLE;5-(2Hydroxyl-5methylphenyl)-isoxazole
• CAS NO: 104516-57-6
• Molecular Formula: C₁₀H₉NO₂
• Molecular Weight: 175.18
• Mol File: 104516-57-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 319.5 °C at 760 mmHg
• Flash Point: 147 °C
• Appearance: /
• Density: 1.204 g/cm³
• CAS DataBase Reference: 2-(5-ISOXAZOLYL)-4-METHYLPHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(5-ISOXAZOLYL)-4-METHYLPHENOL(104516-57-6)
• EPA Substance Registry System: 2-(5-ISOXAZOLYL)-4-METHYLPHENOL(104516-57-6)

Safety Data

• Hazardous Substances Data: 104516-57-6(Hazardous Substances Data)

Usage

General Description

2-(5-ISOXAZOLYL)-4-METHYLPHENOL, also known as teclozan, is a chemical compound with the molecular formula C10H9NO2. It is a synthetic organic compound that belongs to the class of phenols and isoxazoles. Teclozan is commonly used as an anti-infective agent, particularly as an antimicrobial agent against protozoa and helminths. It has been used to treat infections caused by parasites, including giardiasis and trichomoniasis. Additionally, teclozan has been studied for its potential use in the treatment of tuberculosis. The compound is commercially available in the form of tablets and is primarily used in the field of veterinary medicine.

Upstream product

• 90843-41-7 3-(2-hydroxy-5-methyl-phenyl)-3-oxo-propionaldehyde 
• 38445-23-7 6-methyl-chromen-4-one 
• 213689-90-8 (E)-3-Diethylamino-1-(2-hydroxy-5-methyl-phenyl)-propenone 
• 89807-39-6 (2E)-3-(dimethylamino)-1-(2-hydroxy-5-methylphenyl)-2-propen-1-one 
• 1450-72-2 5-methyl-2-hydroxyacetophenone 
• 89807-39-6 1-(2-hydroxy-5-methylphenyl)-3-(N,N-dimethylamino)propenone 

Downstream Products

• 164171-61-3 3-(2-hydroxy-5-methylphenyl)-3-oxopropanenitrile 

Relevant articles and documents

Zn(OTf)2-Catalyzed Formal [3 + 3] Cascade Annulation of Propargylic Alcohols with 2-Aminochromones: Accessing the Chromeno[2,3- b]pyridines

A Zn(OTf)2-catalyzed formal [3 + 3] cascade annulation strategy for the synthesis of functionalized chromeno[2,3-b]pyridines has been developed using propargylic alcohols and 2-aminochromones as the substrates. The protocol provides a convenien

Synthesis of substituted isoxazoles and 1,3,4-oxadiazoles

A few novel 5-(2'-hydroxyaryl)-isoxazoles 3 and 2-(aryloxymethyl)-3-mercapto-1,3,4-oxadiazoles 8 have been synthesized from the intermediate enamino ketones 2, and tested for their herbicidal activity

The Reaction of S,S-Diphenylsulphilimine with Benzopyran-4-ones and Benzopyran-4-thiones

Benzopyran-4-ones unsubstituted at carbons 2 and 3 yield aziridines, amines and isoxazoles on treatment with diphenylsulphilimine.The product composition is temperature dependent, aziridines being the major products at room temperature and amines at highe