51110-60-2

Usage

Uses

Used in Chemical Industry:
2-Methyl-1,3-benzoxazol-4-ol is used as an intermediate in organic synthesis for various applications in the chemical industry. Its aromatic nature and stability make it a valuable compound for the synthesis of other organic compounds.
Used in Pharmaceutical Industry:
2-Methyl-1,3-benzoxazol-4-ol is used as a building block in the development of pharmaceutical compounds. Its unique structure and properties can be exploited to create new drugs with potential therapeutic applications.
Used in Research and Development:
2-Methyl-1,3-benzoxazol-4-ol is used as a research compound in academic and industrial laboratories. Its properties and reactivity can be studied to gain insights into the behavior of similar aromatic compounds and to develop new synthetic methods and applications.
Used in Material Science:
2-Methyl-1,3-benzoxazol-4-ol is used as a component in the development of new materials with specific properties, such as electronic, optical, or mechanical characteristics. Its incorporation into materials can lead to the creation of novel materials with potential applications in various industries.

Upstream product

• 22233-82-5 1-(2,6-dihydroxyphenyl)ethan-1-one oxime 
• 60-35-5 acetamide 
• 699-83-2 2,6-dihydroxylacetophenone 
• 601-89-8 2-nitroresorcinol 
• 3163-15-3 2-aminoresorcinol 
• 123-54-6 acetylacetone 

Downstream Products

• 1190841-30-5 C₂₃H₂₅N₃O₄ 

Relevant academic research and scientific papers

ALPHA, BETA-UNSATURATED AMIDE COMPOUND

An object of the present invention is to provide an α,β-unsaturated amide compound or a pharmaceutically acceptable salt or the like thereof having anticancer activity and the like. The α,β-unsaturated amide compound represented by the following formula (I) or a pharmaceutically acceptable salt or the like thereof has anticancer activity and the like: [wherein, "A" represents optionally substituted heterocyclic diyl, R1 represents hydrogen atom or optionally substituted lower alkyl, R2 represents optionally substituted aryl, optionally substituted cycloalkyl, optionally substituted aliphatic heterocyclic group or optionally substituted aromatic heterocyclic group, X represents -O-, -S-, -SO2-, -NRX1- (wherein, RX1 represents hydrogen atom or lower alkyl), -CHRX2- (wherein, RX2 represents hydrogen atom or hydroxy), -CH=CH-, -CO- or -NH-CO-, and n1 and n2 are the same or different, and each represents 0 or 1].

Utility of Nitrogen Extrusion of Azido Complexes for the Synthesis of Nitriles, Benzoxazoles, and Benzisoxazoles

The utility of the nitrogen extrusion reaction of azido complexes, generated in situ from the corresponding aldehydes or ketones with TMSN3 in the presence of ZrCl4 or TfOH, has been described. These azido complexes could undergo three different pathways, depending on the substrates. First, azido methanolate complexes or imine diazonium ions could lead to benzisoxazole products via an intramolecular nucleophilic substitution. Second, imine diazonium ions could also undergo either the elimination of proton to provide nitrile products in good to excellent yields or an aryl migration, followed by an intramolecular nucleophilic addition, to give benzoxazole products in good yields.

DISULFONAMIDES USEFUL IN THE TREATMENT OF INFLAMMATION

There is provided compounds of formula (I), wherein the A ring, X1, X2, R1, R2, Cx, Qy, T1 and T2 have meanings given in the description, and pharmaceutically-acceptab