1718-54-3

Basic information

• Product Name: 9-Anthracenamine, 10-phenyl-
• CAS NO: 1718-54-3
• Molecular Formula: C20H15N
• Molecular Weight: 0.00000
• Mol File: 1718-54-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 9-Anthracenamine, 10-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 9-Anthracenamine, 10-phenyl-(1718-54-3)
• EPA Substance Registry System: 9-Anthracenamine, 10-phenyl-(1718-54-3)

Safety Data

• Hazardous Substances Data: 1718-54-3(Hazardous Substances Data)

Upstream product

• 591-50-4 iodobenzene 
• 6393-50-6 α-lithiophenylacetonitrile 
• 108-86-1 bromobenzene 
• 71104-10-4 C₄₀H₂₇NO 
• 90292-76-5 2-benzhydryl-benzonitrile 
• 134450-66-1 9-phenyl-10-nitroanthracene 

Downstream Products

• 96176-28-2 Imid des 10-Benzoyloxy-10-phenyl-anthrons-⁽⁹⁾ 
• 96176-05-5 10-Benzoyloxy-10-phenyl-anthron-⁽⁹⁾ 
• 77130-72-4 10,10'-diphenyl-10,10'-peroxy-di-anthrone 
• 4708-42-3 <10-Phenyl-anthryl-(9)>-<10-imino-9-phenyl-9,10-dihydro-anthryl-(9)>-amin 
• 58848-25-2 10-hydroperoxy-10-phenyl-anthrone-imine 

Relevant articles and documents

Iodine ate complexes and N-lithiobenzocyclobutenamine intermediates in the reactions of α-lithionitriles with benzyne

α-Lithionitriles add to benzynes to give N-lithiobenzocyclobutenamines in a two-step process. The intermediate aryllithiums can be trapped prior to cyclization with iodobenzene or 2,6-dimethoxyiodobenzene to form iodine-ate complex intermediates which fragment preferentially to 2-(α-cyanobenzyl)-iodobenzenes. The N-lithiobenzocyclobutenamines undergo ring opening to yield either 2-substituted benzonitriles or α-substituted benzylcyanides depending on the substitution pattern on the aryl and cyclobutene rings. (C) 2000 Published by Elsevier Science Ltd.