56759-33-2

Usage

Uses

Used in Organic Synthesis:
3'-Bromo-4'-nitroacetophenone is used as a key intermediate in organic synthesis for the production of a variety of complex organic molecules. Its unique structure allows for multiple reaction pathways, facilitating the creation of diverse chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3'-Bromo-4'-nitroacetophenone is utilized as a starting material for the development of new pharmaceuticals. Its potential as a building block enables the synthesis of novel drug candidates with potential therapeutic applications.
Used in Agrochemical Production:
3'-Bromo-4'-nitroacetophenone is also employed in the agrochemical sector as a precursor for the synthesis of various agrochemicals. Its reactivity and structural features contribute to the development of effective compounds for agricultural use.
Used in Medicinal Chemistry:
3'-Bromo-4'-nitroacetophenone has been studied for its potential biological activities, which may have implications in medicinal chemistry. Its exploration in this field could lead to the discovery of new therapeutic agents with significant medical applications.

Upstream product

• 56759-32-1 1-(4-amino-3-bromophenyl)-ethanone 
• 99-92-3 p-aminobenzophenone 
• 89978-51-8 4-Nitro-3-brom-ethylbenzol 

Downstream Products

• 56759-34-3 2-bromo-1-(4-nitro-3-bromophenyl)ethanone 

Relevant academic research and scientific papers

PAN-GENOMIC INHIBITORS OF NS5A PROTEIN ENCODED BY HCV, PHARMACEUTICAL COMPOSITIONS, INTERMEDIATES FOR INHIBITOR SYNTHESIS, AND THEIR SYNTHESIS AND APPLICATION METHODS.

Compound represented by formula 1 : or a pharmaceutically acceptable salt, a hydrate, a crystalline form, or a stereoisomer thereof, wherein: where R11 is an optionally substituted C1-C6 alkyl, an optionally substituted C3-C6 cycloalkyl, or an optionally substituted C1-C6 alkyloxy, and arrows (1-C4alkyl; R3 is an optionally substituted aryl, an optionally substituted aryloxy, an optionally substituted arylsulfanyl, an optionally substituted arylamino, or an optionally substituted nitrogen hetaryl; where R41 is an optionally substituted C1-C6 alkyl, an optionally substituted C3-C6 cycloalkyl, or an optionally substituted C1-C6 alkyloxy; X is buta-1,3-diynylene or 1,4-phenylene; arrows (— ) indicate the position of substituents attachment.

FUSED INDOLE COMPOUNDS AND METHODS OF USING SAME

The invention relates to fused indole compounds of formula (I) that can be used for treating microbial infections, in particular, fungal infections, and selectively kill cancer cells.

CARBAZOLE COMPOUNDS AND METHODS OF USING SAME

The invention relates to carbazole compounds of formula (I) that can be used for treating microbial infections, in particular, fungal infections, and selectively kill cancer cells.

CARBAZOLE COMPOUNDS AND METHODS OF USING SAME

The present invention provides carbazole compounds of the formula (I), which can be used for treating microbial, protozoan, viral infections and cancer. ?