1195-56-8

Basic information

• Product Name: 3,3,5,5-TETRAMETHYLPIPERIDINE
• Synonyms: 3,3,5,5-TETRAMETHYLPIPERIDINE;Piperidine, 3,3,5,5-tetraMethyl-
• CAS NO: 1195-56-8
• Molecular Formula: C9H19N
• Molecular Weight: 141.25386
• Product Categories: Miscellaneous Reagents
• Mol File: 1195-56-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3,3,5,5-TETRAMETHYLPIPERIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3,5,5-TETRAMETHYLPIPERIDINE(1195-56-8)
• EPA Substance Registry System: 3,3,5,5-TETRAMETHYLPIPERIDINE(1195-56-8)

Safety Data

• Hazardous Substances Data: 1195-56-8(Hazardous Substances Data)

Usage

Uses

3,3,5,5-Tetramethylpiperidine (cas# 1195-56-8) is a compound useful in organic synthesis.

Upstream product

• 141366-86-1 1-benzyl-3,3,5,5-tetramethylglutarimide 
• 141366-87-2 1-benzyl-3,3,5,5-tetramethylpiperidine 

Downstream Products

• 1622872-33-6 C₃₆H₄₆N₂O₄ 
• 1622872-55-2 C₄₆H₅₅N₃O₅ 
• 1622872-45-0 C₁₆H₂₃NO₂ 
• 1622872-40-5 C₁₇H₂₂F₃NO 

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.