1225462-92-9

Basic information

• Product Name: 6-bromo-3,4-diphenylisoquinolin-1(2H)-one
• Synonyms: 6-bromo-3,4-diphenylisoquinolin-1(2H)-one
• CAS NO: 1225462-92-9
• Molecular Weight: 376.252
• Mol File: 1225462-92-9.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 6-bromo-3,4-diphenylisoquinolin-1(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-bromo-3,4-diphenylisoquinolin-1(2H)-one(1225462-92-9)
• EPA Substance Registry System: 6-bromo-3,4-diphenylisoquinolin-1(2H)-one(1225462-92-9)

Safety Data

• Hazardous Substances Data: 1225462-92-9(Hazardous Substances Data)

Upstream product

• 623-00-7 4-bromobenzenecarbonitrile 
• 501-65-5 diphenyl acetylene 
• 1836-27-7 4-bromo-N-hydroxybenzamide 
• 69673-99-0 4-bromo-N’-(4-bromobenzoyl)benzohydrazide 
• 33341-65-0 4-bromo-N-chlorobenzamide 
• 698-67-9 p-bromobenzamide 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 5933-32-4 4-bromobenzoic acid hydrazide 
• 63295-61-4 4-bromo-benzoic acid-[1]naphthylamide 
• 14917-59-0 p-bromobenzoyl azide 
• 586-75-4 4-chlorobenzoyl chloride 
• 586-76-5 4-Bromobenzoic acid 
• 72755-10-3 4-bromo-N-methoxybenzamide 
• 1328746-00-4 N-methoxy-4-(trifluoromethyl)benzamide 

Downstream Products

• 1280681-87-9 C₃₁H₂₂BrNO₃ 

Relevant articles and documents

2-(1-Methylhydrazinyl)pyridine as a reductively removable directing group in a cobalt-catalyzed C(sp2)-H bond alkenylation/annulation cascade

We describe a new application of 2-(1-methylhydrazinyl)pyridine as a bidentate directing group to directing cobalt-catalyzed C(sp2)-H alkenylation/annulation of the corresponding benzoic hydrazides to form an isoquinoline backbone, via reacting

Synthesis of isoquinolone via rhodium(III)-catalyzed C-H activation with 1,4,2-dioxazol-5-ones as oxidizing directing group

An efficient rhodium-catalyzed direct C-H activation for the synthesis of isoquinolone with 1,4,2-dioxazol-5-ones as oxidizing directing groups have been developed, which featured mild reaction conditions, short reaction time and satisfactory yield.

Direct access to cobaltacycles via C-H activation: N-chloroamide- enabled room-temperature synthesis of heterocycles

Cobaltacycle synthesis via C-H activation has been achieved for the first time, providing key mechanistic insight into cobalt catalytic chemistry. NChloroamides are used as a directing synthon for cobalt-catalyzed roomtemperature C-H activation and construction of heterocycles. Alkynes as coupling partners allow convenient access to isoquinolones, a class of synthetically and pharmaceutically important compounds. The broad substrate scope enables a diverse range of substitution patterns to be incorporated into the heterocyclic scaffold.