121787-54-0

Basic information

• Product Name: phenyl(10-phenylphenanthren-9-yl)methanonephenyl(10-phenylphenanthren-9-yl)methanone
• CAS NO: 121787-54-0
• Molecular Weight: 358.439
• Mol File: 121787-54-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: phenyl(10-phenylphenanthren-9-yl)methanonephenyl(10-phenylphenanthren-9-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl(10-phenylphenanthren-9-yl)methanonephenyl(10-phenylphenanthren-9-yl)methanone(121787-54-0)
• EPA Substance Registry System: phenyl(10-phenylphenanthren-9-yl)methanonephenyl(10-phenylphenanthren-9-yl)methanone(121787-54-0)

Safety Data

• Hazardous Substances Data: 121787-54-0(Hazardous Substances Data)

Upstream product

• 122335-90-4 phenyl-(10-phenyl-9,10-dihydro-[9]phenanthryl)-ketone 
• 876499-26-2 1,2,3,3-tetraphenylprop-2-en-1-ol 
• 16331-54-7 phenanthrene-9-carbonyl chloride 
• 102184-00-9 phenyl phenanthrene-9-carboxylate 
• 98-80-6 phenylboronic acid 
• 90-41-5 2-phenylaniline 
• 536-74-3 phenylacetylene 
• 21375-88-2 1-bromo-2-(phenylethenyl)benzene 

Downstream Products

• 67961-32-4 phenylindenophenanthrene 

Relevant articles and documents

Iron-catalyzed tandem carbon-carbon/carbon-oxygen bond formation/aromatization of 2′-alkynyl-biphenyl-2-carbinols: A new approach to the synthesis of substituted phenanthrenes

An iron-catalyzed efficient synthesis of substituted phenanthrenes through tandem intramolecular C-C/C-O bond formations/aromatization of 2′-alkynyl-biphenyl-2-carbinols is reported. This method provides a novel, highly efficient, and straightforward rout

Sequential multiple-photon photochemistry of sterically congested enones

The photochemistry of sterically hindered enones 1 and 2 is described. A novel photorearrangement occurs in both systems which involves carbonyl attack on the adjacent phenyl ring, expansion of that ring to a cycloheptatriene and subsequent photochemically induced 1,7-phenyl migration.