87768-46-5

Basic information

• Product Name: Benzamide, N-[(1S)-1-(methoxymethyl)-2-methylpropyl]-
• CAS NO: 87768-46-5
• Molecular Formula: C13H19NO2
• Molecular Weight: 221.299
• Mol File: 87768-46-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzamide, N-[(1S)-1-(methoxymethyl)-2-methylpropyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-[(1S)-1-(methoxymethyl)-2-methylpropyl]-(87768-46-5)
• EPA Substance Registry System: Benzamide, N-[(1S)-1-(methoxymethyl)-2-methylpropyl]-(87768-46-5)

Safety Data

• Hazardous Substances Data: 87768-46-5(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 1185294-54-5 1-(1-methylethoxy)-3-phenyl-2-propylamine hydrochloride 
• 64715-88-4 (S)-2-amino-1-methoxy-3-methylbutane 
• 2026-48-4 (S)-valinol 
• 149182-41-2 (S)-N-(1-hydroxy-3-methylbutan-2-yl)benzamide 
• 74-88-4 methyl iodide 

Downstream Products

• 386253-22-1 N-[(1S)-1-(methoxymethyl)-2-methylpropyl]-N-[(1E)-[(2R)-2-methylpyridin-1(2H)-yl](phenyl)methylene]amine 
• 386253-33-4 (E)-N-[(2S)-1-methoxy-3-methylbutan-2-yl]-1-[(2R)-2-ethylpyridin-1(2H)-yl]-1-phenylmethanimine 
• 386253-35-6 (S)-N-(((S)-2-(furan-2-yl)pyridin-1(2H)-yl)(phenyl)methylene)-1-methoxy-3-methylbutan-2-amine 
• 386253-34-5 (S)-1-methoxy-3-methyl-N(phenyl((S)-2-phenylpyridin-1(2H)-yl)methylene)butan-2-amine 
• 777944-33-9 N-(1E)-[(2R)-3-{[3,5-bis(trifluoromethyl)benzyl]oxy}-2-phenyl-2H-pyridin-1-yl]-N-[(S)-2-(1-methoxy-3-methylbutyl)]-benzamidine 
• 849774-32-9 N-[(1S)-1-(methoxymethyl)-2-methylpropyl]-N-{(1E)-phenyl[(2R)-2-phenyl-3-[(triisopropylsilyl)oxy]pyridin-1(2H)-yl]methylene}amine 
• 93-55-0 1-phenyl-propan-1-one 
• 1185294-54-5 1-(1-methylethoxy)-3-phenyl-2-propylamine hydrochloride 

Relevant articles and documents

Tf2O-Mediated Intermolecular Coupling of Secondary Amides with Enamines or Ketones: A Versatile and Direct Access to β-Enaminones

Based on the Tf2O-mediated intermolecular reaction of secondary amides with enamines derived from ketones, a novel approach to β-enaminones has been developed. The reaction is widely functional group tolerant and highly chemoselective. In the presence of 4 ? molecular sieves, the method can be extended to the one-pot condensation of secondary amides with ketones for NH β-enaminones synthesis.

Practical and highly regio- and stereoselective synthesis of 2-substituted dihydropyridines and piperidines: Application to the synthesis of (-)-coniine [17]

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