24451-64-7

Upstream product

• 60-29-7 diethyl ether 
• 16603-23-9 10-benzyl-9(10H)-anthracenone 
• 860208-16-8 10-Phenyl-9-benzyl-9.10-dihydro-anthranol-⁽⁹⁾ 
• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 
• 72948-69-7 9-Benzyliden-10-phenyl-9,10-dihydro-anthracen 
• 7664-93-9 sulfuric acid 
• 10034-85-2 hydrogen iodide 
• 87223-05-0 1-Benzyl-8,9,12-triphenyl-9,12-diaza-tricyclo[6.2.2.0^2,7]dodeca-2⁽⁷⁾,3,5-triene-10,11-dione 
• 98-88-4 benzoyl chloride 
• 602-55-1 9-phenylanthracene 
• 4159-04-0 10-Methylene-10H-anthracen-9-one 
• 87223-10-7 4-Benzyl-1,2-diphenyl-2H-isoquinolin-3-one 
• 87223-11-8 C₃₄H₂₅NO 

Downstream Products

• 7467-97-2 9-(α-bromo-benzyl)-10-phenyl-anthracene 

Relevant academic research and scientific papers

MESOIONIC SIX-MEMBERED HETEROCYCLES, XVII. CYCLOADDITION OF BENZYNE TO MESOIONIC PYRIMIDINES

Benzyne (1) reacts with mesoionic pyrimidines (2a-e) yielding below 40 deg C the primary cycloadducts 3a-e.At higher temperatures the isoquinolin-3-ones 4a-e are formed under the loss of phenyl isocyanate.Further adition of 1 to 4e yields the adduct 5, wh

Reactions of (9-Anthryl)arylmethyl Chloride and Its Homologues with Nucleophiles under Solvolytic Conditions. Notable Effects of Reaction Conditions and Substituents on the Reaction Sites

The reactions of (9-anthryl)arylmethyl chlorides 2a-e (the substituents are p-MeO, p-Me, H, p-Cl, and m-Cl), the corresponding bromides 3b-d (the substituents are p-Me, H, and p-Cl), and the antimonate salts 4b-e (the substituents are p-Me, H, p-Cl, and m