141366-86-1

Basic information

• Product Name: 2,6-Piperidinedione, 3,3,5,5-tetramethyl-1-(phenylmethyl)-
• CAS NO: 141366-86-1
• Molecular Formula: C16H21NO2
• Molecular Weight: 259.348
• Mol File: 141366-86-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,6-Piperidinedione, 3,3,5,5-tetramethyl-1-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Piperidinedione, 3,3,5,5-tetramethyl-1-(phenylmethyl)-(141366-86-1)
• EPA Substance Registry System: 2,6-Piperidinedione, 3,3,5,5-tetramethyl-1-(phenylmethyl)-(141366-86-1)

Safety Data

• Hazardous Substances Data: 141366-86-1(Hazardous Substances Data)

Upstream product

• 96326-44-2 3,3-dimethyl-1-(phenylmethyl)-2,6-piperidinedione 
• 74-88-4 methyl iodide 

Downstream Products

• 1195-56-8 3,3,5,5-tetramethylpiperidine 
• 141366-87-2 1-benzyl-3,3,5,5-tetramethylpiperidine 

Relevant articles and documents

Asymmetric synthesis catalyzed by chiral ferrocenylphosphine transition metal complexes. 10 gold(I)-catalyzed asymmetric aldol reaction of isocyanoacetate

Optically active ferrocenylbisphosphine ligands containing 2-(dialkylamino)ethylamino group on the ferrocenylmethyl position have been prepared and used for the gold(I)-catalyzed asymmetric aldol reaction of isocyanoacetate with aldehydes. Six-membered ring amines, such as morpholino or piperidino group, at the terminal of the side chain were most stereoselective to give optically active trans-4- methoxycarbonyl-5-alkyl-2-oxazolines (up to 97% ee) with high enantio- and diastereoselectivity in a quantitative yield.