74625-87-9

Basic information

• Product Name: 3H-Indol-3-one, 6-chloro-2-phenyl-, 1-oxide
• CAS NO: 74625-87-9
• Molecular Formula: C14H8ClNO2
• Molecular Weight: 257.676
• Mol File: 74625-87-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3H-Indol-3-one, 6-chloro-2-phenyl-, 1-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: 3H-Indol-3-one, 6-chloro-2-phenyl-, 1-oxide(74625-87-9)
• EPA Substance Registry System: 3H-Indol-3-one, 6-chloro-2-phenyl-, 1-oxide(74625-87-9)

Safety Data

• Hazardous Substances Data: 74625-87-9(Hazardous Substances Data)

Upstream product

• 74599-01-2 3-(4-Chloro-2-nitro-phenyl)-3-oxo-2-phenyl-propionaldehyde 
• 536-74-3 phenylacetylene 
• 74599-12-5 (4-chloro-2-nitrophenyl)(3-phenyloxiran-2-yl)methanone 
• 74599-26-1 (E)-1-(4-Chloro-2-nitro-phenyl)-3-phenyl-propenone 
• 23082-51-1 4'-chloro-2'-nitroacetophenone 

Downstream Products

• 1402730-71-5 C₂₃H₁₇ClN₂O₂ 
• 1402730-69-1 C₂₂H₁₅ClN₂O₂ 

Relevant articles and documents

Catalytic asymmetric formal [3+2] cycloaddition of isatogens with azlactones to construct indolin-3-one derivatives

The chiral amide-guanidine-catalyzed asymmetric formal [3+2] cycloaddition of isatogens with azlactones is presented. This strategy provided a facile and feasible route to chiral indolin-3-one derivatives bearing two contiguous tetrasubstituted stereocent

AuBr3-catalyzed cyclization of o-(alkynyl)nitrobenzenes. Efficient synthesis of isatogens and anthranils

The cyclization of o-(arylalkynyl)nitrobenzenes was catalyzed by AuBr3 to produce the corresponding isatogens in good to high yields together with small amounts of anthranils. On the other hand, anthranils were obtained selectively when the AuB