17543-99-6

Basic information

• Product Name: 2-[(1E)-2-aza-2-(2-pyridyl)ethenyl]-4-bromobenzen-1-ol
• Synonyms: 2-[(1E)-2-aza-2-(2-pyridyl)ethenyl]-4-bromobenzen-1-ol
• CAS NO: 17543-99-6
• Molecular Weight: 277.12
• Mol File: 17543-99-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-[(1E)-2-aza-2-(2-pyridyl)ethenyl]-4-bromobenzen-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(1E)-2-aza-2-(2-pyridyl)ethenyl]-4-bromobenzen-1-ol(17543-99-6)
• EPA Substance Registry System: 2-[(1E)-2-aza-2-(2-pyridyl)ethenyl]-4-bromobenzen-1-ol(17543-99-6)

Safety Data

• Hazardous Substances Data: 17543-99-6(Hazardous Substances Data)

Upstream product

• 504-29-0 2-aminopyridine 
• 1761-61-1 5-bromosalicyclaldehyde 

Relevant articles and documents

C-H?Br-C: Vs. C-Br?Br-C vs. C-Br?N bonding in molecular self-assembly of pyridine-containing dyes

We have studied a series of closely related N-(5-bromosalicylidene)-x-aminopyridine compounds (x = 2, 1; 3, 2; 4, 3), obtained by condensation of 5-bromosalicylaldehyde with the corresponding aminopyridine. 1H NMR spectroscopy in solution revea

Synthesis, spectral studies of salicylidine-pyridines: Crystal and molecular structure of 2-[(1E)-2-aza-2-(5-methyl(2-pyridyl)ethenyl)]-4-bromobenzen-1-ol

Schiff bases derived from different meta-substituted salicylaldehyde and 5-methylaminopyridine have been synthesized and characterized by elemental analysis, FT-IR, NMR and UV-vis techniques. NMR assignments were made using 1H, 13C N

Hydrogen Bonding and Tautomeric Equilibria in Schiff Bases Derived from 2-Aminopyridines: Electronic Spectral Evidence for Substituent Effects

Schiff bases of the type C6H3(R)(OH)CH=NC5H3N(Y) have now been synthesised and evidence sought for th