7115-13-1

Basic information

• Product Name: 3-Phenylisocarbostyril
• CAS NO: 7115-13-1
• Molecular Weight: 221.258
• Mol File: 7115-13-1.mol
• Article Data: 51

Chemical Properties

• CAS DataBase Reference: 3-Phenylisocarbostyril(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Phenylisocarbostyril(7115-13-1)
• EPA Substance Registry System: 3-Phenylisocarbostyril(7115-13-1)

Safety Data

• Hazardous Substances Data: 7115-13-1(Hazardous Substances Data)

Upstream product

• 23994-23-2 3-phenyl-isoquinoline-1,4-dione 
• 4809-08-9 3-phenyl-isocoumarin 
• 855623-26-6 4-hydroxy-3-phenyl-3,4-dihydro-2H-isoquinolin-1-one 
• 245122-81-0 1-ethoxy-3-phenylisoquinoline 
• 80221-08-5 2-(2-phenylethynyl)benzamide 
• 2728-04-3 N,N-diethyl-ortho-toluamide 
• 158109-78-5 (R,E)-N-benzylidene-4-methylbenzenesulfinamide 
• 3930-83-4 o-iodobenzamide 
• 98-86-2 acetophenone 
• 167558-57-8 1,1-Dibromo-2-(o-carboxamidophenyl)ethene 
• 98-80-6 phenylboronic acid 
• 6302-55-2 1-(4'-chlorophenyl)-1,3-butanedione 
• 99-91-2 para-chloroacetophenone 
• 93-91-4 1-phenylbutan-1,3-dione 

Downstream Products

• 181371-82-4 4-Nitro-3-phenyl-2H-isoquinolin-1-one 
• 55150-54-4 1-chloro-3-phenylisoquinoline 
• 26060-10-6 3-phenyl-2-(prop-2-ynyl)-isoquinolin-1-(2H)-one 
• 181371-86-8 ICC₁08-L-006-C₀₅- 
• 181372-12-3 N-(1-Oxo-3-phenyl-1,2-dihydro-isoquinolin-4-yl)-acetamide 
• 181372-02-1 (3-Phenyl-isoquinolin-4-yl)-carbamic acid ethyl ester 
• 181371-90-4 (1-Oxo-3-phenyl-1,2-dihydro-isoquinolin-4-yl)-carbamic acid ethyl ester 
• 181371-99-3 (1-Chloro-3-phenyl-isoquinolin-4-yl)-carbamic acid ethyl ester 
• 78318-00-0 3-phenyl-1,2,3,4-tetrahydroisoquinoline 
• 85741-16-8 2-Nitroso-3-phenyl-1,2,3,4-tetrahydroisoquinoline 
• 85741-19-1 [1-(4-Nitro-phenyl)-meth-(E)-ylidene]-(3-phenyl-3,4-dihydro-1H-isoquinolin-2-yl)-amine 
• 85741-17-9 2-amino-3-phenyl-1,2,3,4-tetrahydroisoquinoline hydrochloride 
• 34497-10-4 2-methyl-3-phenylisoquinolin-1(2H)-one 
• 1352288-06-2 3-(2-methyl-1-oxo-3-phenyl-1,2-dihydro-isoquinolin-4-yl)-2-phenyl-acrylonitrile 

Relevant articles and documents

One-pot synthesis of 3-substituted isoquinolin-1-(2H)-ones and fused isoquinolin-1-(2H)-ones by SRN1 reactions in DMSO

3-Substituted isoquinolin-1-(2H)-ones and fused isoquinolin-1-(2H)-ones have been obtained by the photostimulated SRN1 reactions of 2-iodobenzamide with the enolates of aromatic (acetophenone, 1-(benzo[d][1,3]dioxol-5-yl)ethanone, 1- and 2-naph

Synthesis and Application of Heterocyclic Germatranes via Rhodium-Catalyzed Directed C?H Activation/Annulation with Alkynyl Germatranes and Palladium-Catalyzed Cross-Coupling

Rhodium-catalyzed C?H activation and annulation with alkynyl germatranes for the synthesis of heterocyclic germatranes is described. Various heterocyclic germatranes were constructed by this protocol and applied in multiple derivatizations such as palladi

Triflic acid mediated sequential cyclization of ortho-alkynylarylesters with ammonium acetate

A triflic acid (TfOH) mediated sequential cyclization of ortho-alkynylarylesters and ammonium acetate (NH4OAc) was reported. The reaction took place via a Br?nsted acid-mediated intramolecular cyclization of ortho-alkynylarylesters followed by an ammonium acetate participated substitution reaction, forming isoquinolin-1-ones as the major products. Different from most of the known synthetic methods of isoquinolin-1-ones, no metal catalyst was required in the reported reaction. The regioisomers – isoindolin-1-ones were obtained together with isoquinolin-1-ones in a few cases. The intermediate compounds – isochromen-1-ones and isobenzofuran-1-ones were also isolated. The interconversion experiments showed that the regioisomers formed during the Br?nsted acid induced intramolecular cyclization of ortho-alkynylarylesters. A natural product – ruprechstyril was prepared in a moderate yield employing the new method.