188296-54-0

Basic information

• Product Name: N,N-diallyl-N-(3-fluoro)aniline
• Synonyms: N,N-diallyl-N-(3-fluoro)aniline
• CAS NO: 188296-54-0
• Molecular Weight: 191.248
• Mol File: 188296-54-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N,N-diallyl-N-(3-fluoro)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-diallyl-N-(3-fluoro)aniline(188296-54-0)
• EPA Substance Registry System: N,N-diallyl-N-(3-fluoro)aniline(188296-54-0)

Safety Data

• Hazardous Substances Data: 188296-54-0(Hazardous Substances Data)

Upstream product

• 372-19-0 meta-fluoroaniline 
• 107-05-1 3-chloroprop-1-ene 
• 106-95-6 allyl bromide 

Downstream Products

• 53871-27-5 1-(3-fluorophenyl)-1H-pyrrole 

Relevant articles and documents

A general approach to substituted diphenyldiazenes

A general and practical synthetic method for the construction of unsymmetrically substituted diphenyldiazenes based on classical azo coupling reaction has been developed. A key feature of this method is the use of N,N-diallyl protected aniline derivatives

Assisted tandem catalytic RCM-aromatization in the synthesis of pyrroles and furans

An assisted tandem catalytic transformation of diallyl amines and diallyl ethers into N-aryl pyrroles and furans, respectively, is described. The sequence relies on ring closing metathesis followed by dehydrogenation of the initially formed dihydropyrroles and dihydrofurans. Both steps are Ru-catalyzed, but the sequence requires only one precatalyst, because conversion of the metathesis catalyst into the dehydrogenation catalyst is achieved in situ, triggered by the oxidant tert-butyl hydroperoxide.