1542227-80-4

Basic information

• Product Name: (2S)-{1-[2-(3-[1,3]dioxolan-2-yl-pyridin-2-yl)-4,5-dimethoxy-phenylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester
• Synonyms: (2S)-{1-[2-(3-[1,3]dioxolan-2-yl-pyridin-2-yl)-4,5-dimethoxy-phenylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester
• CAS NO: 1542227-80-4
• Molecular Weight: 549.624
• Mol File: 1542227-80-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S)-{1-[2-(3-[1,3]dioxolan-2-yl-pyridin-2-yl)-4,5-dimethoxy-phenylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-{1-[2-(3-[1,3]dioxolan-2-yl-pyridin-2-yl)-4,5-dimethoxy-phenylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester(1542227-80-4)
• EPA Substance Registry System: (2S)-{1-[2-(3-[1,3]dioxolan-2-yl-pyridin-2-yl)-4,5-dimethoxy-phenylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester(1542227-80-4)

Safety Data

• Hazardous Substances Data: 1542227-80-4(Hazardous Substances Data)

Upstream product

• 51072-66-3 1-bromo-4,5-dimethoxy-2-nitro-benzene 
• 2859-78-1 4-Bromoveratrole 
• 128071-75-0 2-bromopyridine-3-carboxaldehyde 
• 865449-15-6 2-bromo-3-(dibromomethyl)-pyridine 
• 1542227-73-5 2-(3-[1,3]dioxolan-2-yl-pyridin-2-yl)-4,5-dimethoxy-phenylamine 
• 85613-64-5 (S)-3-(tert-butoxycarbonyl)amino-4-phenyl-2-butanone 
• 1542227-72-4 2-(4,5-dimethoxy-2-nitro-phenyl)-3-[1,3]dioxolan-2-yl-pyridine 
• 3430-17-9 2-bromo-3-picoline 
• 1542227-71-3 2-(4,5-dimethoxy-2-nitro-phenyl)-pyridine-3-carbaldehyde 
• 1542227-70-2 C₂₀H₃₅NO₄Sn 

Relevant articles and documents

Diastereoselective synthesis of rotationally restricted chiral phenylpyridines via intramolecular cascade cyclization of n-acyliminium ions containing α-amino acid residues

A series of chiral phenylpyridines possessing a fused chiral bridge were synthesized diastereoselectively via cascade cyclizations, where N-acyliminium ions including an enantiopure α-amino acid residue were involved. The absolute configuration of the synthesized phenylpyridines was identified unambiguously by using nuclear Overhauser effect difference and circular dichroism (CD) measurements on the basis of literature methods. Taylor & Francis Group, LLC.