1599-33-3

Basic information

• Product Name: (2-methylpiperidin-1-yl)(phenyl)methanone
• CAS NO: 1599-33-3
• Molecular Weight: 203.284
• Mol File: 1599-33-3.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: (2-methylpiperidin-1-yl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2-methylpiperidin-1-yl)(phenyl)methanone(1599-33-3)
• EPA Substance Registry System: (2-methylpiperidin-1-yl)(phenyl)methanone(1599-33-3)

Safety Data

• Hazardous Substances Data: 1599-33-3(Hazardous Substances Data)

Upstream product

• 109-06-8 α-picoline 
• 98-88-4 benzoyl chloride 
• 3197-42-0 (S)-2-methylpiperidine 
• 100-52-7 benzaldehyde 
• 109-05-7 2-Methylpiperidin 
• 65-85-0 benzoic acid 
• 1000789-28-5 C₁₂H₁₆ClNS 
• 120986-91-6 B(OC₂H₅)2(CH₂)4CH(N₃)CH₃ 
• 5119-88-0 2-methylpiperidine hydrochloride 

Downstream Products

• 627-96-3 1,5-dibromohexane 
• 100-47-0 benzonitrile 
• 13729-76-5 N-Benzoyl-2-methyl-4-piperidon 
• 54305-90-7 1,5-dichloro-hexane 
• 92041-66-2 6-benzoylamino-5-methylpentanoic acid 
• 1019351-96-2 (2-hydroxy-phenyl)-(2-methyl-piperidin-1-yl)-methanone 

Relevant articles and documents

Diboron-Catalyzed Dehydrative Amidation of Aromatic Carboxylic Acids with Amines

Tetrakis(dimethylamido)diboron and tetrahydroxydiboron are herein reported as new catalysts for the synthesis of aryl amides by catalytic condensation of aromatic carboxylic acids with amines. The developed protocol is both simple and highly efficient over a broad range of substrates. This method thus represents an attractive approach for the use of diboron catalysts in the synthesis of amides without having to resort to stoichiometric or additional dehydrating agents.

DECONSTRUCTIVE FUNCTIONALIZATION METHODS AND COMPOUNDS

Disclosed herein, inter alia, are deconstructive functionalization methods and compounds made using the same.

Cross-Dehydrogenating Coupling of Aldehydes with Amines/R-OTBS Ethers by Visible-Light Photoredox Catalysis: Synthesis of Amides, Esters, and Ureas

A straightforward synthesis of amides, ureas, and esters is reported by visible-light cross-dehydrogenating coupling (CDC) of aldehydes (or amine carbaldehydes) and amines/R-OTBS ethers by photoredox catalysis. The reaction is found to be general and high yielding. A plausible mechanistic pathway has been proposed for these transformations and is supported by appropriate controlled experiments.