335200-15-2

Basic information

• Product Name: 2H-Cycloheptoxazol-2-one,octahydro-8a-methyl-,(3aR,8aS)-rel-(9CI)
• Synonyms: 2H-Cycloheptoxazol-2-one,octahydro-8a-methyl-,(3aR,8aS)-rel-(9CI)
• CAS NO: 335200-15-2
• Molecular Formula: C9H15NO2
• Molecular Weight: 169.2209
• Product Categories: N-BOC
• Mol File: 335200-15-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2H-Cycloheptoxazol-2-one,octahydro-8a-methyl-,(3aR,8aS)-rel-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Cycloheptoxazol-2-one,octahydro-8a-methyl-,(3aR,8aS)-rel-(9CI)(335200-15-2)
• EPA Substance Registry System: 2H-Cycloheptoxazol-2-one,octahydro-8a-methyl-,(3aR,8aS)-rel-(9CI)(335200-15-2)

Safety Data

• Hazardous Substances Data: 335200-15-2(Hazardous Substances Data)

Usage

Structure

Cyclic compound with a seven-membered ring containing a nitrogen and an oxygen atom

Stereochemistry

(3aR,8aS)-rel configuration indicating a specific 3D arrangement of atoms

Potential applications

Drug discovery and development, research in organic chemistry

Further studies needed

To fully understand properties and potential uses

Upstream product

• 502-42-1 cycloheptanone 
• 3761-94-2 1-methylcycloheptanol 

Relevant articles and documents

Controllable Intramolecular Unactivated C(sp3)-H Amination and Oxygenation of Carbamates

Dual catalyst-controlled intramolecular unactivated C(sp3)-H amination and oxygenation of carbamates merging visible-light photocatalysis and earth-abundant transition metal catalysis have been reported. Useful amino alcohol and diol derivatives could be selectively obtained from readily available tertiary alcohol derivatives. The possible mechanisms have been proposed via a 1,5-HAT process followed by Lewis acid-controlled cyclization. The nickel and zinc catalysts inhibit the formation of oxygenation and amination products, respectively. An interesting phenomenon of chirality transfer is also observed.