1341218-06-1

Basic information

• Product Name: tert-butyl (S)-2,6-dioxo-1-phenethylpiperidin-3-ylcarbamate
• Synonyms: tert-butyl (S)-2,6-dioxo-1-phenethylpiperidin-3-ylcarbamate
• CAS NO: 1341218-06-1
• Molecular Weight: 332.4
• Mol File: 1341218-06-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tert-butyl (S)-2,6-dioxo-1-phenethylpiperidin-3-ylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (S)-2,6-dioxo-1-phenethylpiperidin-3-ylcarbamate(1341218-06-1)
• EPA Substance Registry System: tert-butyl (S)-2,6-dioxo-1-phenethylpiperidin-3-ylcarbamate(1341218-06-1)

Safety Data

• Hazardous Substances Data: 1341218-06-1(Hazardous Substances Data)

Upstream product

• 60-12-8 2-phenylethanol 
• 151367-92-9 L-tert-butyl N-[2,6-dioxohexahydro-3-pyridinyl] Carbamate 
• 13726-85-7 Boc-Gln-OH 
• 103-63-9 1-phenyl-2-bromoethane 

Downstream Products

• 1175950-31-8 C₁₃H₁₆N₂O₂ 
• 51870-97-4 (S)-N-(2,6-dioxo-1-phenethylpiperidin-3-yl)isobutyramide 
• 1000974-41-3 (S)-N-(2,6-dioxo-1-phenethylpiperidin-3-yl)propionamide 
• 492-87-5 N-[(3S)-2,6-dioxo-1-(2-phenylethyl)-3-piperidinyl]-(2S)-2-methylbutanamide 

Relevant articles and documents

Enantioselective synthesis of glutarimide alkaloids cordiarimides A, B, crotonimides A, B, and julocrotine

Five glutarimide alkaloids cordiarimide A (5), cordiarimide B (6), crotonimide A (3), crotonimide B (4), and julocrotine (2) have been synthesized starting from Boc-L-glutamine (7). The benzylic alcohol chiral centre of cordiarimides B (6) has been established in 6:1 diastereoselectivity by catalytic asymmetric hydrogenation using Zhou's catalytic system Pd(CF 3CO2)2/(R,R)-Me-DuPhos. Copyright