CAS 626-67-5
:N-Méthylpipéridine
- 1-Methylpiperidin
- 1-Methylpiperidine
- 1-Methylpiperidine Hydrochloride (1:1)
- 1-Methylpiperidinium
- 1-Metilpiperidina
- N-Methylpiperidin
- Piperidine, 1-methyl-
- Piperidine, Methyl
- N-Methylpiperidine
1-Methylpiperidine
CAS :Formule :C6H13NDegré de pureté :>99.0%(GC)(T)Couleur et forme :Colorless to Light yellow clear liquidMasse moléculaire :99.181-Methylpiperidine, 99%
CAS :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
Formule :C6H14ClNDegré de pureté :99%Couleur et forme :Clear colorless to yellow, LiquidMasse moléculaire :135.64N-Methylpiperidine
CAS :Produit contrôléFormule :C6H13NCouleur et forme :NeatMasse moléculaire :99.174N-Methylpiperidine
CAS :Formule :C6H13NDegré de pureté :99.0%Couleur et forme :LiquidMasse moléculaire :99.1771-Methylpiperidine
CAS :Produit contrôléFormule :C6H13NCouleur et forme :ColourlessMasse moléculaire :99.174N-Methylpiperidine
CAS :N-Methylpiperidine is a nitrogenous organic compound that belongs to the group of p2. It has a molecular weight of 82.07 and a melting point of -8 °C. The nmr spectra show that the proton is in the p-hydroxybenzoic acid moiety and not in the piperidinium moiety. N-Methylpiperidine has been shown to have tuberculostatic activity. It may also be carcinogenic, but it has not been proven yet. This chemical substance can be synthesized by reacting hydrochloric acid with carboxylic acids, such as p-hydroxybenzoic acid or amines, or by reacting aniline with methyl halide and potassium hydroxide.
Formule :C6H13NDegré de pureté :Min. 95%Masse moléculaire :99.17 g/mol







