1318251-47-6

Basic information

• Product Name: 3-ethyl-5-(4-fluorophenyl)-1,3-dimethylindolin-2-one
• Synonyms: 3-ethyl-5-(4-fluorophenyl)-1,3-dimethylindolin-2-one
• CAS NO: 1318251-47-6
• Molecular Weight: 283.345
• Mol File: 1318251-47-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-ethyl-5-(4-fluorophenyl)-1,3-dimethylindolin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ethyl-5-(4-fluorophenyl)-1,3-dimethylindolin-2-one(1318251-47-6)
• EPA Substance Registry System: 3-ethyl-5-(4-fluorophenyl)-1,3-dimethylindolin-2-one(1318251-47-6)

Safety Data

• Hazardous Substances Data: 1318251-47-6(Hazardous Substances Data)

Upstream product

• 4411-99-8 2-ethyl-2-butenoic acid 
• 4390-96-9 2-ethylacryloyl chloride 
• 110-05-4 di-tert-butyl peroxide 
• 1582285-74-2 C₁₇H₁₆FNO 
• 22326-72-3 3-ethyl-1,3-dimethylindolin-2-one 
• 1318251-50-1 5-bromo-3-ethyl-1,3-dimethylindolin-2-one 
• 1765-93-1 4-fluoroboronic acid 

Relevant articles and documents

A tethering directing group strategy for ruthenium-catalyzed intramolecular alkene hydroarylation

We report a new catalyst design for N-heterocycle synthesis that utilizes an alkene-tethered amide moiety as a directing group for aromatic C-H activation. This tethering directing group strategy is demonstrated in a ruthenium-catalyzed intramolecular alk

A convenient enantioselective synthesis of 3-asymmetrically substituted oxindoles as progesterone receptor antagonists

A convenient enantioselective synthesis of 3-asymmetrically substituted oxindoles is reported. Compound (2) prepared by radical cyclisation of (1) was used for the synthesis of racemic and enantiomerically pure 3-asymmetrically substituted oxindoles. Desu