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2,2,6,6-Tetramethylpiperidine, 98+%, Thermo Scientific Chemicals
5g, Each
Thermo Scientific Chemicals
2,2,6,6-Tetramethylpiperidine, 98+%, Thermo Scientific Chemicals
5g, Each
Quantity
Catalog number: A18712.06
also known as A18712-06
Price (USD)
Price: 37.30
Your Price:
Quantity
-
Chemical Identifiers
CAS
768-66-1
IUPAC Name
2,2,6,6-tetramethylpiperidine
Molecular Formula
C9H19N
InChI Key
RKMGAJGJIURJSJ-UHFFFAOYSA-N
SMILES
CC1(C)CCCC(C)(C)N1
Specifications
Specification SheetAssay (GC)
≥98.0%
Appearance (Color)
Clear colorless to pale yellow
Identification (FTIR)
Conforms
Refractive Index
1.4425-1.4465 @ 20?C
Form
Liquid
Description
2,2,6,6-Tetramethylpiperidine is a hindered base used to prepare metallo-amide bases and selective generation of silylketene acetals. It is used in the preparation of hibarimicinone, (Z)-silylketene acetal and 4-substituted quinazoline. It acts as a precursor to Lithium tetramethylpiperidide and (2,2,6,6-Tetramethylpiperidin-1-yl)oxyl radical.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2,2,6,6-Tetramethylpiperidine is a hindered base used to prepare metallo-amide bases and selective generation of silylketene acetals. It is used in the preparation of hibarimicinone, (Z)-silylketene acetal and 4-substituted quinazoline. It acts as a precursor to Lithium tetramethylpiperidide and (2,2,6,6-Tetramethylpiperidin-1-yl)oxyl radical.
Solubility
Miscible with water, ether, ethanol and acetic acid. Slightly miscible with chloroform.
Notes
Incompatible with oxidizing agents, bases, strong acids, acid anhydrides, carbon dioxide and acid chlorides.
2,2,6,6-Tetramethylpiperidine is a hindered base used to prepare metallo-amide bases and selective generation of silylketene acetals. It is used in the preparation of hibarimicinone, (Z)-silylketene acetal and 4-substituted quinazoline. It acts as a precursor to Lithium tetramethylpiperidide and (2,2,6,6-Tetramethylpiperidin-1-yl)oxyl radical.
Solubility
Miscible with water, ether, ethanol and acetic acid. Slightly miscible with chloroform.
Notes
Incompatible with oxidizing agents, bases, strong acids, acid anhydrides, carbon dioxide and acid chlorides.
RUO – Research Use Only