101209-08-9

Usage

Uses

Used in Pharmaceutical Synthesis:
4-Acetamido-3-bromoacetophenone is used as a key intermediate in the production of various pharmaceuticals. Its unique structure and reactivity allow for the creation of a wide range of molecules with different therapeutic properties.
Used in Organic Synthesis:
As a versatile building block, 4-Acetamido-3-bromoacetophenone is utilized in the synthesis of a diverse array of organic compounds. Its structural features enable the development of molecules with specific functions and applications in various fields.
Used in Medicinal Chemistry:
4-Acetamido-3-bromoacetophenone is employed as a valuable component in medicinal chemistry, where its reactivity and structural attributes contribute to the design and synthesis of new molecules with potential therapeutic applications.
Used in Drug Discovery:
4-Acetamido-3-bromoacetophenone plays a significant role in drug discovery, where its unique properties can be leveraged to identify and develop new drugs with improved efficacy and selectivity.

InChI:InChI=1/C10H10BrNO2/c1-6(13)8-3-4-10(9(11)5-8)12-7(2)14/h3-5H,1-2H3,(H,12,14)

Upstream product

• 103-89-9 4-Methylacetanilide 
• 7726-95-6 bromine 
• 64-19-7 acetic acid 
• 2719-21-3 4-(N-acetylamino)acetophenone 

Downstream Products

• 56759-32-1 1-(4-amino-3-bromophenyl)-ethanone 
• 74103-28-9 3-bromo-4-acetamidobenzoic acid 
• 89250-35-1 N-[2-Bromo-4-(2-bromo-acetyl)-phenyl]-acetamide 
• 20077-92-3 2-methylbenzothiazol-5-yl methyl ketone 
• 130623-32-4 N-[2-Bromo-4-(5,6-dihydro-imidazo[2,1-b]thiazol-3-yl)-phenyl]-acetamide; hydrobromide 
• 130623-09-5 N-{2-Bromo-4-[2-(4,5-dihydro-1H-imidazol-2-ylsulfanyl)-acetyl]-phenyl}-acetamide; hydrobromide 
• 1352873-05-2 N-{5-acetyl-4'-[3-(2-chloro-benzyl)-2-imino-2,3-dihydro-benzoimidazol-1-yl]-biphenyl-2-yl}-acetamide 
• 93273-64-4 4-acetyl-2-bromobenzoic acid 
• 93273-63-3 4-acetyl-2-bromobenzonitrile 
• 1100768-15-7 N-(1-{3-bromo-4-[(piperidine-4-carbonyl)-amino]-phenyl}-ethyl)-N'-(4-carbamimidoyl-phenyl)-malonamide trifluoroacetate 
• 1100768-32-8 N-{1-[3-bromo-4-(morpholine-4-carbonyl)-phenyl]-ethyl}-N'-(4-carbamimidoyl-phenyl)-malonamide trifluoroacetate 
• 1100768-17-9 4-[4-(1-amino-ethyl)-2-bromo-phenylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester 
• 1100768-33-9 1-[3-bromo-4-(morpholine-4-carbonyl)-phenyl]-ethanone 
• 1100768-34-0 [4-(1-amino-ethyl)-2-bromo-phenyl]-morpholin-4-yl-methanone 

Relevant academic research and scientific papers

Palladium-catalyzed ortho-halogenations of acetanilides with N-halosuccinimides via direct sp2 C–H bond activation in ball mills

A solvent-free palladium-catalyzed ortho-iodination of acetanilides using N-iodosuccinimide as the iodine source has been developed under ball-milling conditions. This present method avoids the use of hazardous organic solvents, high reaction temperature,