1044507-64-3

Basic information

• Product Name: tert-butyl-3-(4-fluorophenyl)azetidine-1-carboxylate
• Synonyms: tert-butyl-3-(4-fluorophenyl)azetidine-1-carboxylate
• CAS NO: 1044507-64-3
• Molecular Weight: 251.301
• Mol File: 1044507-64-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: tert-butyl-3-(4-fluorophenyl)azetidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl-3-(4-fluorophenyl)azetidine-1-carboxylate(1044507-64-3)
• EPA Substance Registry System: tert-butyl-3-(4-fluorophenyl)azetidine-1-carboxylate(1044507-64-3)

Safety Data

• Hazardous Substances Data: 1044507-64-3(Hazardous Substances Data)

Upstream product

• 1765-93-1 4-fluoroboronic acid 
• 254454-54-1 tert-butyl-3-iodoazetidine-1-carboxylate 
• 352-13-6 4-flourophenylmagnesium bromide 
• 141699-55-0 tert-butyl 3-hydroxyazetidine-1-carboxylate 
• 214360-58-4 2-(4-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Downstream Products

• 1203796-58-0 3-(4-fluorophenyl)azetidine 

Relevant articles and documents

Merging Halogen-Atom Transfer (XAT) and Copper Catalysis for the Modular Suzuki-Miyaura-Type Cross-Coupling of Alkyl Iodides and Organoborons

We report here a mechanistically distinct approach to achieve Suzuki-Miyaura-type cross-couplings between alkyl iodides and aryl organoborons. This process requires a copper catalyst but, in contrast with previous approaches based on palladium and nickel

Iron- and cobalt-catalyzed arylation of azetidines, pyrrolidines, and piperidines with grignard reagents

Iron- and cobalt-catalyzed cross-couplings between iodo-azetidines, -pyrrolidines, -piperidines, and Grignard reagents are disclosed. The reaction is efficient, cheap, chemoselective and tolerates a large variety of (hetero)aryl Grignard reagents.