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Usage

Uses

Used in Pharmaceutical Industry:
1-(2-fluoro-3-nitrophenyl)ethanone is used as a starting material for the synthesis of pharmaceuticals, due to its versatile chemical properties and reactivity. The presence of the fluorine and nitro groups allows for the creation of various biologically active molecules, making it a valuable component in the development of new drugs.
Used in Dye Industry:
1-(2-fluoro-3-nitrophenyl)ethanone is used as a starting material for the preparation of dyes, as its chemical structure can be modified to produce a wide range of colors and properties. This makes it a valuable component in the creation of new dyes for various applications.
Used in Organic Synthesis:
1-(2-fluoro-3-nitrophenyl)ethanone is used as an intermediate in organic synthesis, as its reactivity and chemical properties allow for the production of a wide range of chemical products. This makes it a valuable building block for the synthesis of various organic compounds.

Upstream product

• 58534-94-4 2-fluoro-3-bromonitrobenzene 
• 97674-02-7 tributyl(1-ethoxyvinyl)stannane 
• 943769-01-5 C₁₀H₁₀FNO₃ 

Downstream Products

• 1336804-14-8 2-bromo-1-(2-fluoro-3-nitrophenyl)ethanone 
• 1262098-06-5 3-amino-2-fluoroacetophenone 

Relevant academic research and scientific papers

IMINOTETRAHYDROPYRIMIDINONE DERIVATIVES AS PLASMEPSIN V INHIBITORS

A series of 2-imino-6-methyltetrahydropyrimidin-4(lH)-one derivatives, substituted in the 6-position by a phenyl moiety which in turn is meta-substituted by an optionally substituted unsaturated fused bicyclic ring system containing at least one nitrogen atom, being selective inhibitors of plasmepsin V activity, are beneficial as pharmaceutical agents, especially in the treatment of malaria.

Compounds for kinase modulation, and indications therefor

Compounds active on protein kinases and methods for regulating protein kinase pathways are described, as well as methods of using such compounds to treat diseases and conditions associated with aberrant activity of protein kinases.

Compounds, Compositions and Methods

Certain substituted urea derivatives modulate the cardiac sarcomere, for example by potentiating cardiac myosin, and are useful in the treatment of systolic heart failure including congestive heart failure.

CERTAIN CHEMICAL ENTITIES, COMPOSITIONS AND METHODS

Certain substituted urea derivatives modulate diskeletal myosin, skeletal actin, skeletal tropomyosin, skeletal troponin C, skeletal troponin I, skeletal troponin T, and skeletal muscle, including fragments and isoforms thereof, as well as the skeletal sarcomere, and are useful in the treatment of obesity, sarcopenia, wasting syndrome, frailty, muscle spasm, cachexia, neuromuscular diseases (e.g., amyotrophic lateral sclerosis, spinal muscular atrophy, familial or acquired myopathies or muscular dystrophies), post-surgical and post-traumatic muscle weakness, and other conditions.

CERTAIN CHEMICAL ENTITIES, COMPOSITIONS AND METHODS

Certain substituted urea derivatives selectively modulate the cardiac sarcomere, for example by potentiating cardiac myosin, and are useful in the treatment of systolic heart failure including congestive heart failure.

CERTAIN CHEMICAL ENTITIES, COMPOSITIONS AND METHODS

Certain substituted urea derivatives selectively modulate the cardiac sarcomere, for example by potentiating cardiac myosin, and are useful in the treatment of systolic heart failure including congestive heart failure.

COMPOUNDS, COMPOSITIONS AND METHODS

Certain substituted urea derivatives selectively modulate the cardiac sarcomere, for example by potentiating cardiac myosin, and are useful in the treatment of systolic heart failure including congestive heart failure.

Compounds, compositions and methods

Certain substituted urea derivatives selectively modulate the cardiac sarcomere, for example by potentiating cardiac myosin, and are useful in the treatment of systolic heart failure including congestive heart failure.

Substituted alkylaryl ketones and methods of use as herbicides

Ring and side chain substituted alkylaryl ketones are useful in controlling the growth of germinating and seedling weed grasses and germinating and seedling broadleaf weeds.