13355-65-2

Basic information

• Product Name: 5-phenylphenanthridin-6(5H)-one
• CAS NO: 13355-65-2
• Molecular Formula: C₁₉H₁₃NO
• Molecular Weight: 271.3126
• Mol File: 13355-65-2.mol
• Article Data: 21

Chemical Properties

• Boiling Point: 468.9°C at 760 mmHg
• Flash Point: 226.7°C
• Density: 1.245g/cm³
• Vapor Pressure: 5.74E-09mmHg at 25°C
• Refractive Index: 1.676
• CAS DataBase Reference: 5-phenylphenanthridin-6(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-phenylphenanthridin-6(5H)-one(13355-65-2)
• EPA Substance Registry System: 5-phenylphenanthridin-6(5H)-one(13355-65-2)

Safety Data

• Hazardous Substances Data: 13355-65-2(Hazardous Substances Data)

Upstream product

• 13355-64-1 5-phenyl-5,6-dihydrophenanthridine 
• 609-67-6 2-Iodobenzoyl chloride 
• 62-53-3 aniline 
• 88-65-3 2-bromobenzoic-acid 
• 118-91-2 ortho-chlorobenzoic acid 
• 93-98-1 N-phenyl benzoyl amide 
• 583-55-1 1-Bromo-2-iodobenzene 
• 98-88-4 benzoyl chloride 
• 947-84-2 2-Biphenylcarboxylic acid 
• 110490-31-8 2-(3-phenyl-triazenyl)-benzoic acid methyl ester 
• 19263-30-0 3-phenyl-1,2,3-benzotriazin-4(3H)-one 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 134-20-3 2-carbomethoxyaniline 
• 13234-80-5 N-phenyl-[1,1′-biphenyl]-2-carboxamide 

Relevant articles and documents

TBAB-Mediated Radical 5-exo-trig ipso-Cyclization of 2-Arylbenzamide for the Synthesis of Spiro[cyclohexane-1,1′-isoindoline]-2,5-diene-3′,4-dione

A TBAB-mediated radical 5-exo-trig ipso-cyclization of N-aryl-2-arylbenzamide is described herein for the synthesis of spiro[cyclohexane-1,1′-isoindoline]-2,5-diene-3′,4-dione. The transformation proceeds regioselectively and provides the final products w

Phenanthrapyridones derivatives, synthetic method thereof and electronic device containing phenanthrapyridones derivatives (by machine translation)

The phenanthrapyridones derivatives of, the present invention can be used for the synthesis of the phenanthones derivatives of the present invention. as the, electron blocking layers (1) or: electron ,L1 transport L2 layers of the electron blocking, layer

NIS-mediated oxidative arene C(sp2)-H amidation toward 3,4-dihydro-2(1H)-quinolinone, phenanthridone, and N-fused spirolactam derivatives

A new radical-mediated intramolecular arene C(sp2)-H amidation of 3-phenylpropanamides or [1,1′-biphenyl]-2-carboxamides was developed to prepare a series of 3,4-dihydro-2(1H)-quinolinone and phenanthridone derivatives in moderate to excellent yields (33-94%). Spirolactams could also be obtained using this protocol.