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1-Methylpiperidine, 99%, Thermo Scientific Chemicals
Catalog number: L03398.22
100 g, Each
Thermo Scientific Chemicals
1-Methylpiperidine, 99%, Thermo Scientific Chemicals
Catalog number: L03398.22
100 g, Each
Quantity
Catalog number: L03398.22
also known as L03398-22
Price (USD)
Price: 50.10
Online price: 42.65
Your price:
Quantity
-
Chemical Identifiers
CAS
626-67-5
IUPAC Name
hydrogen 1-methylpiperidine chloride
Molecular Formula
C6H14ClN
InChI Key
QDUXDCXILAPLAG-UHFFFAOYSA-N
SMILES
[H+].[Cl-].CN1CCCCC1
Specifications
Specification SheetAppearance (Color)
Clear colorless to yellow
Form
Liquid
Assay (GC)
>98.5%
Refractive Index
1.4360-1.4390 @ 20?C
Description
1-Methylpiperidine is a reactant for sp3 C-H Bond activation with ruthenium(II) catalysts and C(3)-alkylation of cyclic amines, One-pot synthesis of Z-cinnamic acids. It is used in the synthesis of Unsymmetrical ureas, Antibacterial imidazolium, pyrrolidinium, and piperidinium salts, C1-C16 segment of goniodomin A via palladium-catalyzed organostannane thioester coupling.
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
1-Methylpiperidine is a reactant for sp3 C-H Bond activation with ruthenium(II) catalysts and C(3)-alkylation of cyclic amines, One-pot synthesis of Z-cinnamic acids. It is used in the synthesis of Unsymmetrical ureas, Antibacterial imidazolium, pyrrolidinium, and piperidinium salts, C1-C16 segment of goniodomin A via palladium-catalyzed organostannane thioester coupling.
Solubility
Fully miscible in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with.acids, Acid chlorides, Acid anhydrides, Strong oxidizing agents, Carbon dioxide.
1-Methylpiperidine is a reactant for sp3 C-H Bond activation with ruthenium(II) catalysts and C(3)-alkylation of cyclic amines, One-pot synthesis of Z-cinnamic acids. It is used in the synthesis of Unsymmetrical ureas, Antibacterial imidazolium, pyrrolidinium, and piperidinium salts, C1-C16 segment of goniodomin A via palladium-catalyzed organostannane thioester coupling.
Solubility
Fully miscible in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with.acids, Acid chlorides, Acid anhydrides, Strong oxidizing agents, Carbon dioxide.
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