1037586-23-4

Basic information

• Product Name: 2-bromo-N-(2-bromophenyl)-butyramide
• Synonyms: 2-bromo-N-(2-bromophenyl)-butyramide
• CAS NO: 1037586-23-4
• Molecular Weight: 321.011
• Mol File: 1037586-23-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-bromo-N-(2-bromophenyl)-butyramide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-N-(2-bromophenyl)-butyramide(1037586-23-4)
• EPA Substance Registry System: 2-bromo-N-(2-bromophenyl)-butyramide(1037586-23-4)

Safety Data

• Hazardous Substances Data: 1037586-23-4(Hazardous Substances Data)

Upstream product

• 26074-52-2 2-bromo-butyryl bromide 
• 615-36-1 2-bromoaniline 

Downstream Products

• 1037586-68-7 C₁₄H₁₉BrN₂O 
• 1037586-70-1 C₁₄H₁₉BrN₂O₂ 
• 1037586-84-7 C₁₈H₁₇BrN₂O 
• 1037586-74-5 C₁₈H₁₉BrN₂O 
• 1037586-69-8 C₁₄H₂₁BrN₂O 
• 1037586-71-2 C₁₉H₂₈BrN₃O₃ 

Relevant articles and documents

Facile and general synthesis of quaternary 3-aminooxindoles

(Chemical Equation Presented) A novel approach to the valuable quaternary 3-aminooxindole skeleton is reported on the basis of intramolecular arylation of enolates of substituted amino acids. The reaction tolerates dialkyl- and arylalkylamines as well as a range of carbon substituents (primary and secondary alkyl, aryl). The cyclization of N-indolyl-substituted substrates is accompanied by direct C-H arylation of the indole, leading to indolo-fused benzodiazepines.