1312417-53-0

Basic information

• Product Name: 3-allyl-5-methoxy-1-methyl-3-phenylindolin-2-one
• Synonyms: 3-allyl-5-methoxy-1-methyl-3-phenylindolin-2-one
• CAS NO: 1312417-53-0
• Molecular Weight: 293.365
• Mol File: 1312417-53-0.mol

Chemical Properties

• CAS DataBase Reference: 3-allyl-5-methoxy-1-methyl-3-phenylindolin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-allyl-5-methoxy-1-methyl-3-phenylindolin-2-one(1312417-53-0)
• EPA Substance Registry System: 3-allyl-5-methoxy-1-methyl-3-phenylindolin-2-one(1312417-53-0)

Safety Data

• Hazardous Substances Data: 1312417-53-0(Hazardous Substances Data)

Upstream product

• 20423-72-7 1,3-dihydro-5-methoxy-1-methyl-3-phenyl-2H-indol-2-one 
• 51479-73-3 allyl trichloroacetimidate 
• 591-87-7 Allyl acetate 
• 1312417-60-9 C₁₆H₁₆BrNO₂ 

Relevant articles and documents

BF3·Et2O catalyzed allylation of oxindoles with allyl trichloroacetimidate

An efficient Lewis acid catalyzed allylation of 3-substituted oxindoles has been developed for the first time using allyl trichloroacetimidate as an electrophile under mild reaction conditions.

Efficient synthesis of esermethole and its analogues

In this work, a general and flexible synthetic route towards the synthesis of pyrroloindoline alkaloids was developed. This new strategy features with a palladium mediated sequential arylation-allylation of o-bromoanilides and leads to the construction of oxindoles bearing a full carbon quaternary center. The cheap triphenylphosphine was proved to be a highly effective ligand for this one pot transformation. On the basis of this new method, esermethole and its analogues were synthesized.