1439377-39-5

Basic information

• Product Name: 5-bromo-3-(pyridin-2-ylmethyl)-3-(4-(3-(pyridin-4-yl)propyl)phenyl)indolin-2-one
• Synonyms: 5-bromo-3-(pyridin-2-ylmethyl)-3-(4-(3-(pyridin-4-yl)propyl)phenyl)indolin-2-one
• CAS NO: 1439377-39-5
• Molecular Weight: 498.422
• Mol File: 1439377-39-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-bromo-3-(pyridin-2-ylmethyl)-3-(4-(3-(pyridin-4-yl)propyl)phenyl)indolin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-bromo-3-(pyridin-2-ylmethyl)-3-(4-(3-(pyridin-4-yl)propyl)phenyl)indolin-2-one(1439377-39-5)
• EPA Substance Registry System: 5-bromo-3-(pyridin-2-ylmethyl)-3-(4-(3-(pyridin-4-yl)propyl)phenyl)indolin-2-one(1439377-39-5)

Safety Data

• Hazardous Substances Data: 1439377-39-5(Hazardous Substances Data)

Upstream product

• 109-06-8 α-picoline 
• 2057-49-0 4-(3-phenylpropyl)pyridine 
• 99304-31-1 α-(2-oxo-3-hydroxy-(5-bromo)indolinyl<3>)-2-methylpyridine 
• 87-48-9 5-Bromo-1H-indole-2,3-dione 

Relevant articles and documents

Preparation of aryl-substituted 2-oxyindoles by superelectrophilic chemistry

A series of pyridyl-substituted 3-hydroxy-2-oxyindoles have been prepared and reacted with arenes in superacid promoted Friedel-Crafts reactions. The product aryl-substituted 2-oxyindoles are formed in generally good yields. With substituted arenes such as toluene, bromobenzene, or ethyl salicylate, the Friedel-Crafts reactions occur with excellent regioselectivity. A mechanism is proposed involving dicationic, superelectrophilic species leading to the electrophilic aromatic substitution chemistry.