1240659-41-9

Basic information

• Product Name: 6-(tert-butyldimethylsilyloxy)-3-(4-fluorophenyl)hexan-2-one
• Synonyms: 6-(tert-butyldimethylsilyloxy)-3-(4-fluorophenyl)hexan-2-one
• CAS NO: 1240659-41-9
• Molecular Weight: 324.511
• Mol File: 1240659-41-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-(tert-butyldimethylsilyloxy)-3-(4-fluorophenyl)hexan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(tert-butyldimethylsilyloxy)-3-(4-fluorophenyl)hexan-2-one(1240659-41-9)
• EPA Substance Registry System: 6-(tert-butyldimethylsilyloxy)-3-(4-fluorophenyl)hexan-2-one(1240659-41-9)

Safety Data

• Hazardous Substances Data: 1240659-41-9(Hazardous Substances Data)

Upstream product

• 459-03-0 4-fluorophenyl acetone 
• 78878-05-4 1-iodo-3-(tert-butyldimethylsilyloxy)propane 

Downstream Products

• 1240659-42-0 2-(6-(tert-butyldimethylsilyloxy)-3-(4-fluorophenyl)hexan-2-ylidene)-1,1-dimethylhydrazine 

Relevant articles and documents

Fe(II)-catalyzed amination of aromatic C-H bonds via ring opening of 2 H-azirines: Synthesis of 2,3-disubstituted indoles

A general method for the synthesis of 2,3-disubstituted indoles is described. The key feature of this method is the amination of aromatic C-H bonds via FeCl2-catalyzed ring opening of 2H-azirines. The method tolerates a variety of functional groups such as Br, F, NO2, OMe, CF3, OTBS, alkenes, and OPiv. The method can also be extended to synthesize azaindoles.