41498-06-0

Basic information

• Product Name: 5-BROMO-1-NAPHTHALDEHYDE
• Synonyms: 5-BROMO-1-NAPHTHALDEHYDE;5-bromonaphthalene-1-carbaldehyde
• CAS NO: 41498-06-0
• Molecular Formula: C₁₁H₇BrO
• Molecular Weight: 235.08
• Mol File: 41498-06-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-BROMO-1-NAPHTHALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMO-1-NAPHTHALDEHYDE(41498-06-0)
• EPA Substance Registry System: 5-BROMO-1-NAPHTHALDEHYDE(41498-06-0)

Safety Data

• Hazardous Substances Data: 41498-06-0(Hazardous Substances Data)

Upstream product

• 20366-57-8 (5-bromo-naphthalen-1-yl)-methanol 
• 16726-67-3 5-bromo-1-naphthalenecarboxylic acid 
• 86-52-2 1-Chloromethylnaphthalene 
• 91-20-3 naphthalene 
• 64-17-5 ethanol 
• 129278-20-2 5-Bromo-1-cyanonaphthalene 
• 7732-18-5 water 
• 141-78-6 ethyl acetate 
• 56-23-5 tetrachloromethane 
• 84532-82-1 5-bromo-1-naphthoyl chloride 
• 67-66-3 chloroform 
• 7726-95-6 bromine 
• 66-77-3 1-naphthaldehyde 

Downstream Products

• 702707-14-0 5-phenyl-1-naphthaldehyde 
• 1353554-85-4 C₂₂H₂₅N₃ 
• 1353555-96-0 1,3-di-Boc-2-((5-(4-(t-butyl)phenyl)naphthalen-1-yl)methyl)guanidine 
• 1426170-84-4 C₁₉H₁₆F₃NO 
• 1353554-98-9 C₂₀H₁₈F₃N₃ 
• 1353556-19-0 1,3-di-Boc-2-(2-(5-(4-(trifluoromethyl)phenyl)naphthalen-1-yl)ethyl)guanidine 
• 1353554-96-7 C₁₉H₁₆F₃N₃ 
• 1353556-17-8 1,3-di-Boc-2-((5-(4-(trifluoromethyl)phenyl)naphthalen-1-yl)methyl)guanidine 
• 1353554-94-5 C₁₈H₁₆BrN₃ 
• 1353556-11-2 1,3-di-Boc-2-((5-(4-bromophenyl)naphthalen-1-yl)methyl)guanidine 
• 1353554-95-6 C₁₈H₁₆ClN₃ 

Relevant articles and documents

Palladium-Catalyzed Regiospecific peri- And ortho-C-H Oxygenations of Polyaromatic Rings Mediated by Tunable Directing Groups

An efficient divergent approach of Pd-catalyzed C-H oxygenation of polyaromatic rings is described. Reversible directing groups enable regiospecific peri- and ortho-oxygenation to readily access a wide array of polyaromatic phenols without pre- and postmanipulation of directing groups. The systematic mechanistic investigation, including deuterium-labeling experiments, palladacycle trapping, and DFT calculations, reveals that the tunable ligand-assisted C-H bond cleavage played a crucial role during the reaction process.