1161819-40-4

Basic information

• Product Name: (R)-2-(2-tolylaminooxy)cyclohexanone
• Synonyms: (R)-2-(2-tolylaminooxy)cyclohexanone
• CAS NO: 1161819-40-4
• Molecular Weight: 219.283
• Mol File: 1161819-40-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (R)-2-(2-tolylaminooxy)cyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-(2-tolylaminooxy)cyclohexanone(1161819-40-4)
• EPA Substance Registry System: (R)-2-(2-tolylaminooxy)cyclohexanone(1161819-40-4)

Safety Data

• Hazardous Substances Data: 1161819-40-4(Hazardous Substances Data)

Upstream product

• 611-23-4 2-nitrosotoluene 
• 108-94-1 cyclohexanone 

Downstream Products

• 533-60-8 (R)-α-hydroxycyclohexanone 
• 1001025-62-2 (1R,2R)-1-isopropyl-1,2-cyclohexanediol 
• 108392-44-5 (1S,2R)-1-methylcyclohexane-1,2-diol 
• 1161819-44-8 (1R,2R)-1-vinyl-1,2-cyclohexanediol 
• 1161819-42-6 (1R,2R)-1-(t-butyl)-1,2-cyclohexanediol 
• 210101-10-3 (1R,2R)-1-allyl-1,2-cyclohexanediol 
• 4912-59-8 (1R,2R)-1-phenyl-1,2-cyclohexanediol 
• 1001025-63-3 (1R,2R)-1-benzyl-1,2-cyclohexanediol 

Relevant articles and documents

Process Catalyst Mass Efficiency by Using Proline Tetrazole Column-Flow System

Generally, organocatalysts are not decomposed during chemical transformation, which is different from traditional metal catalysts. To improve catalytic processes efficiency, various studies have been applied to flow synthesis for organocatalysis. Furtherm

Asymmetric α-aminoxylations of stoichiometric ketones using 2-nitrosotoluene

Asymmetric aminoxylations of a stoichiometric amount of ketones were accomplished through O-nitrosoaldol reactions of 2-nitrosotoluene catalyzed by a proline-based tetrazole. The advantages of 2-nitrosotoluene and the tetrazole over nitrosobenzene and pro