130850-74-7

Basic information

• Product Name: 7-(2-Chloro-phenyl)-7,14-dihydro-5-oxa-14-aza-dibenzo[a,h]anthracen-6-one
• Synonyms: 7-(2-Chloro-phenyl)-7,14-dihydro-5-oxa-14-aza-dibenzo[a,h]anthracen-6-one
• CAS NO: 130850-74-7
• Molecular Weight: 409.872
• Mol File: 130850-74-7.mol

Chemical Properties

• CAS DataBase Reference: 7-(2-Chloro-phenyl)-7,14-dihydro-5-oxa-14-aza-dibenzo[a,h]anthracen-6-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-(2-Chloro-phenyl)-7,14-dihydro-5-oxa-14-aza-dibenzo[a,h]anthracen-6-one(130850-74-7)
• EPA Substance Registry System: 7-(2-Chloro-phenyl)-7,14-dihydro-5-oxa-14-aza-dibenzo[a,h]anthracen-6-one(130850-74-7)

Safety Data

• Hazardous Substances Data: 130850-74-7(Hazardous Substances Data)

Upstream product

• 1076-38-6 4-hydroxy[1]benzopyran-2-one 
• 27587-15-1 2-(2-chlorobenzylideneamino)naphthalene 

Downstream Products

• 130850-83-8 7-(2-Chloro-phenyl)-5-oxa-14-aza-dibenzo[a,h]anthracen-6-one 

Relevant articles and documents

Clean procedure for synthesis of chromeno[4,3-b]benzo [f]quinolin-6-one derivatives: Reaction of N-arylidenenaphthalen-2-amine with 4-hydroxycoumarin in aqueous media

A short and simple synthesis of chromeno[4,3- b ]benzo[ f ]quinolin-6-one derivatives was accomplished in good to high yields via the reaction of N -arylidenenaphthalen-2-amine with 4-hydroxycoumarin in aqueous media catalyzed by TEBAC. The structures wer

A clean procedure for the synthesis of chromeno[4,3-b]benzo[f]quinoline and quinolino[4,3-b]benzo[f]quinoline derivatives in aqueous media

A short and simple synthesis of chromeno[4,3-b]benzo[f]-quinoline and quinolino[4,3-b]benzo[f]quinoline derivatives were accomplished in high yields via the reaction of N-benzilidenenaphthalen-2-amine and 4-hydroxycoumarin or 4-hydroxyquinolin-2-one in aq

Reaction of β-Arylidennaphthylamines with 4-Hydroxycoumarin. A Correction in Structural Assignment of the Product. III.

The reaction of 4-hydroxycoumarin with β-arylidennaphthylamines constitutes a convenient synthetic route to the hitherto unknown 2H-benzobenzopyranoquinolin-2-one, VI.The X-ray crystallography data conform with the present benzopyranoq