13533-23-8

Basic information

• Product Name: Benzenamine, 4-bromo-N-(2-furanylmethylene)-
• CAS NO: 13533-23-8
• Molecular Formula: C11H8BrNO
• Molecular Weight: 250.095
• Mol File: 13533-23-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-bromo-N-(2-furanylmethylene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-bromo-N-(2-furanylmethylene)-(13533-23-8)
• EPA Substance Registry System: Benzenamine, 4-bromo-N-(2-furanylmethylene)-(13533-23-8)

Safety Data

• Hazardous Substances Data: 13533-23-8(Hazardous Substances Data)

Upstream product

• 98-01-1 furfural 
• 106-40-1 4-bromo-aniline 

Downstream Products

• 31136-77-3 (4-bromo-anilino)-furan-2-yl-acetonitrile 
• 33829-88-8 4-bromo-N-furfuryl-aniline 
• 865353-68-0 (4-bromo-phenyl)-(1-furan-2-yl-3-methyl-but-3-enyl)-amine 
• 865353-80-6 (4-bromo-phenyl)-(1-furan-2-yl-but-3-enyl)-amine 

Relevant articles and documents

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Sulfonic acid supported on hydroxyapatite-encapsulated-γ-Fe 2O3 nanocrystallites as a magnetically separable catalyst for one-pot reductive amination of carbonyl compounds

A novel, environmentally friendly procedure has been developed for the preparation of secondary or tertiary amines by one-pot reductive amination of carbonyl compounds using sodium borohydride in the presence of a magnetically recoverable sulfonic acid supported on hydroxyapatite-encapsulated-γ- Fe2O3 [γ-Fe2O3@HAP-SO 3H] at room temperature. The catalyst was easily separated from the reaction mixture by applying an external magnet and reused for six cycles without significant loss of catalytic activity.

An efficient synthesis of isoindolo[2,1-a]quinoline derivatives via imino Diels-Alder and intramolecular Diels-Alder reactions with furan

The straightforward synthesis of new isoindolo[2,1-a]quinoline derivatives from 2,4-disubstituted 1,2,3,4-tetrahydroquinolines bearing a furan fragment via the intramolecular Diels-Alder reaction is reported. The synthesis of key precursors was realized w