53107-36-1

Usage

Type of compound

Aromatic ketone derivative

Structure

The compound contains a bromine atom and two chlorine atoms on the phenyl ring, a methoxy group, and a methyl group at specific positions.

Uses

It is used in various chemical and pharmaceutical applications, including as an intermediate for the synthesis of other organic compounds. It may also have potential uses in research and development for its unique structure and properties.

Safety precautions

It is important to handle and use this chemical with caution due to its potential health and safety hazards.

Upstream product

• 53107-35-0 2',3',-Dichloro-4'-methoxyisobutyrophenone 
• 1984-59-4 2,3-dichloroanisole 

Downstream Products

• 66015-59-6 [1-Oxo-2-(4-chlorosulfonylphenyl)-2-methyl-6,7-dichloro-5-indanyloxy]acetic acid 
• 66015-32-5 [1-oxo-2-methyl-2-(4-sulfamoylphenyl)-6,7-dichloro-5-indanyloxy]acetic acid 
• 66015-31-4 [1-Oxo-2-(4-aminomethylphenyl)-2-methyl-6,7-dichloro-5-indanyloxy]acetic acid 
• 66015-27-8 [1-oxo-2-(4-methoxyphenyl)-2-methyl-6,7-dichloro-5-indanyloxy]acetic acid 
• 56049-88-8 (+/-)-Indacrinone 
• 66015-52-9 2-(4-methoxyphenyl)-2-methyl-5-hydroxy-6,7-dichloro-1-indanone 
• 57713-17-4 2-methyl-2-phenyl-5-methoxy-6,7-dichloro-1-indanone 
• 57509-50-9 6,7-dichloro-2,3-dihydro-5-hydroxy-2-methyl-2-phenyl-1H-inden-1-one 
• 67976-23-2 2-(4-methoxyphenyl)-2-methyl-5-benzyloxy-6,7-dichloro-1-indanone 
• 61016-62-4 [1-Oxo-2-(4-hydroxyphenyl)-2-methyl-6,7-dichloro-5-indanyloxy]acetic acid 
• 66015-25-6 (+/-)-<<6,7-dichloro-2-(4-fluorophenyl)-2-methyl-1-oxo-5-indanyl>oxy>acetic acid 
• 66015-60-9 (1-oxo-2-methyl-2-phenyl-6,7-dichloro-5-indanyloxy)acetonitrile 
• 58489-84-2 2-(4-chlorophenyl)-2-methyl-5-methoxy-6,7-dichloro-1-indanone 
• 66015-50-7 6,7-dichloro-2-p-fluorophenyl-2,3-dihydro-5-hydroxy-2-methyl-1H-inden-1-one 

Relevant academic research and scientific papers

(1-Oxo-2-aryl or thienyl-2-substituted-5-indanyloxy (or thio) alkanoic acids, and derivatives thereof

[1-Oxo-2-aryl or thienyl-2-substituted-5-indanyloxy (or thio)]aklanoic acid, derivatives thereof, their salts, esters and amides are disclosed. The products display a dual pharmaceutical utility in that they exhibit diuretic, saluretic and uricosuric activity. Also disclosed are processes for the preparation of such [1-oxo-2-aryl or thienyl-2-substituted-5-indanyloxy (or thio)]alkanoic acids, pharmaceutical compositions comprising therapeutically effective amounts of such compounds and methods of treatment comprising administering such compounds and compositions.

[1-Hydroxy-5-indanyloxy (or thio)]-alkanoic acids

[1-Hydroxy-5-indanyloxy (or thio)]alkanoic acids and their salts, esters and amides are disclosed. The products display a dual pharmaceutical utility in that they exhibit diuretic, saluretic and hypouricemic activity. The acid products are prepared by several synthetic methods.

[1-Hydroximino-2,2-disubstituted-5-indanyloxy-(or thio)]alkanoic acids

[1-Hydroximino-2,2-disubstituted-5-indanyloxy-(or thio)]alkanoic acids and their salt, ester, anhydride, amide and 5-tetrazolyl derivatives are disclosed. The products display a dual pharmaceutical utility in that they exhibit diuretic, saluretic and uricosuric activity. The acid products are prepared by treating a 1-oxo-2,2-disubstituted-5-indanyloxy(or thio)alkanoic acids or derivatives thereof with hydroxylamine in the presence of a base.