398489-51-5

Basic information

• Product Name: tert-butyl 3-hydroxy-3-vinylazetidine-1-carboxylate
• Synonyms: tert-butyl 3-hydroxy-3-vinylazetidine-1-carboxylate
• CAS NO: 398489-51-5
• Molecular Formula: C₁₀H₁₇NO₃
• Molecular Weight: 199.24688
• EINECS: -0
• Mol File: 398489-51-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: tert-butyl 3-hydroxy-3-vinylazetidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 3-hydroxy-3-vinylazetidine-1-carboxylate(398489-51-5)
• EPA Substance Registry System: tert-butyl 3-hydroxy-3-vinylazetidine-1-carboxylate(398489-51-5)

Safety Data

• Hazardous Substances Data: 398489-51-5(Hazardous Substances Data)

Upstream product

• 398489-26-4 tert-butyl 3-oxoazetidine-1-carboxylate 
• 1826-67-1 vinyl magnesium bromide 

Downstream Products

• 1453315-91-7 C₁₈H₂₄BrN₃O₄ 

Relevant articles and documents

THERAPEUTIC COMPOUNDS AND COMPOSITIONS AND THEIR USE AS PKM2 MODULATORS

Compositions comprising compounds of general formula (I) that modulate pyruvate kinase are described herein. Also described herein are methods of using the compounds that modulate pyruvate kinase in the treatment of diseases.

Cobalt-catalyzed coupling of alkyl iodides with alkenes: Deprotonation of hydridocobalt enables turnover

Completing the cycle: Cobalt complexes I and II were found to catalyze intramolecular alkyl Heck-type coupling reactions of alkyl iodides to alkenes upon irradiation with visible light in the presence of a tertiary amine base. The use of base is key to the catalytic turnover. The compatibility of the method with a broad range of functional groups opens opportunities for synthesis. Copyright