1613244-34-0

Basic information

• Product Name: 1-(3,4-dihydroquinolin-1(2H)-yl)-3-phenyl-2-(piperidin-1-yl)propan-1-one
• CAS NO: 1613244-34-0
• Molecular Weight: 348.488
• Mol File: 1613244-34-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(3,4-dihydroquinolin-1(2H)-yl)-3-phenyl-2-(piperidin-1-yl)propan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,4-dihydroquinolin-1(2H)-yl)-3-phenyl-2-(piperidin-1-yl)propan-1-one(1613244-34-0)
• EPA Substance Registry System: 1-(3,4-dihydroquinolin-1(2H)-yl)-3-phenyl-2-(piperidin-1-yl)propan-1-one(1613244-34-0)

Safety Data

• Hazardous Substances Data: 1613244-34-0(Hazardous Substances Data)

Upstream product

• 1613244-33-9 benzyl (1-(3,4-dihydroquinolin-1(2H)-yl)-1-oxo-3-phenylpropan-2-yl)carbamate 
• 111-24-0 1,5-dibromo-pentane 
• 1104607-83-1 C₁₈H₂₀N₂O 
• 3588-57-6 Z-DL-Phe-OH 

Relevant articles and documents

Double axial chirality promoted asymmetric [2,3] Stevens rearrangement of N-cinnamyl l-alanine amide-derived ammonium ylides

The base-induced asymmetric [2,3] Stevens rearrangement of N-cinnamyl tetraalkylammonium ylides derived from l-alanine amides proceeds via a double axially chiral intermediate to afford the corresponding α-substituted alanine derivatives with high enantio- and diastereoselectivities. the Partner Organisations 2014.