102074-68-0

Usage

Structure

A derivative of catechol with a methoxy group at the 5-position and an amino group at the 2-position

Usage

Commonly used in the synthesis of various pharmaceuticals and organic compounds

Potential properties

Studied for its antioxidant and antimicrobial properties

Significance

Valuable building block for the production of biologically active substances and research into potential therapeutic uses

Upstream product

• 16600-93-4 1,3-Dihydroxy-5-methoxy-2-nitrobenzene 
• 2174-64-3 5-methoxyresorcinol 

Downstream Products

• 848564-77-2 2-(3-bromo-phenyl)-6-methoxy-benzooxazol-4-ol 
• 460048-04-8 acetamino-5-methoxyresorcinol 
• 848564-78-3 2-(3-bromo-phenyl)-6-methoxy-benzooxazole-4,7-dione 

Relevant academic research and scientific papers

COMPOUNDS HAVING ACTIVITY IN CORRECTING MUTANT CFTR CELLULAR PROCESSING

The present invention relates to a compound which is characterized by the formula (I) or a pharmaceutically acceptable salt, solvate, hydrate thereof, wherein the ring systems A and B are independently selected from a monosaccharide, aryl (preferably phen

Benzothiazole-4,7-diones and benzoxazole-4,7-diones with substituents in position 5 or 6 and method for production thereof

A subject of the invention is a selective process for the preparation of derivatives of benzothiazole-4,7-diones and benzoxazole-4,7-diones monosubstituted in position 5 or in position 6 by an amino group itself optionally substituted. Said derivatives ar

Regioselective preparation of 5-amino- and 6-amino-1,3-benzoxazole-4,7- diones from symmetrical diaminophenol and aminoresorcinol

Regioisomeric 5-amino- and 6-amino- 1,3-benzoxazole-4,7-diones were prepared from 2,6-diamino-4-methoxyphenol and 2-amino-5-methoxyresorcinol, respectively. These symmetrical precursors have the property to be antisymmetrical to each other with respect to