92041-11-7

Basic information

• Product Name: 2-Piperidinemethanol, 1-benzoyl-
• CAS NO: 92041-11-7
• Molecular Formula: C13H17NO2
• Molecular Weight: 219.283
• Mol File: 92041-11-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Piperidinemethanol, 1-benzoyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Piperidinemethanol, 1-benzoyl-(92041-11-7)
• EPA Substance Registry System: 2-Piperidinemethanol, 1-benzoyl-(92041-11-7)

Safety Data

• Hazardous Substances Data: 92041-11-7(Hazardous Substances Data)

Upstream product

• 99720-01-1 methyl N-benzoyl-2-piperidine carboxylate 
• 98-88-4 benzoyl chloride 
• 94685-29-7 N-benzoyl-2-<(benzoyloxy)methyl>piperidine 
• 3433-37-2 piperidin-2-ylmethanol 

Downstream Products

• 474011-77-3 methyl (S)-1-benzoylpiperidine-2-carboxylate 
• 1046767-90-1 N-benzoyl-(2R)-(methoxycarbonyl)piperidine 
• 133787-01-6 N-benzoyl-2-piperidinecarboxaldehyde 
• 1154049-83-8 methyl (N-benzoyl-piperidin-2-yl)acetate 

Relevant articles and documents

Cobalt-Catalyzed Aerobic Oxidative Cleavage of Alkyl Aldehydes: Synthesis of Ketones, Esters, Amides, and α-Ketoamides

A widely applicable approach was developed to synthesize ketones, esters, amides via the oxidative C?C bond cleavage of readily available alkyl aldehydes. Green and abundant molecular oxygen (O2) was used as the oxidant, and base metals (cobalt and copper) were used as the catalysts. This strategy can be extended to the one-pot synthesis of ketones from primary alcohols and α-ketoamides from aldehydes.

HETEROALICYCLIC AMINOALKANOL. II. REACTIONS OF DL-2-PIPERIDIME-METHANOL

-