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Methyl 1-methylpiperidine-3-carboxylate

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Products Intro: Product Name:Methyl N-methyl piperidine-3-carboxylate
CAS:1690-72-8
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Products Intro: Product Name:Methyl 1-methylpiperidine-3-carboxylate
CAS:1690-72-8
Purity:98%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:1690-72-8
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CAS:1690-72-8
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Products Intro: Product Name:Methyl N-methyl piperidine-3-carboxylate
CAS:1690-72-8
Purity:0.98 Package:1kg;5kg;25kg

Methyl 1-methylpiperidine-3-carboxylate manufacturers

Methyl 1-methylpiperidine-3-carboxylate Basic information
Product Name:Methyl 1-methylpiperidine-3-carboxylate
Synonyms:1-methyl-3-piperidinecarboxylicacimethylester;1-methylnipecoticacidmethylester;1-methyl-nipecoticacimethylester;dihydroarecoline;methyln-methylnipecotate;n-methyl-3-carbomethoxypiperidine;1-Methyl-3-Piperidinelarboxylate;1-METHYL-PIPERIDINE-3-CARBOXYLIC ACID METHYL ESTER
CAS:1690-72-8
MF:C8H15NO2
MW:157.21
EINECS:210-314-1
Product Categories:Heterocyclic Compounds
Mol File:1690-72-8.mol
Methyl 1-methylpiperidine-3-carboxylate Structure
Methyl 1-methylpiperidine-3-carboxylate Chemical Properties
Boiling point bp12 83-84°
density 1.013±0.06 g/cm3(Predicted)
refractive index nD25 1.4520
storage temp. 2-8°C
pkapKa (20°): 8.66
AppearanceColorless to light yellow Liquid
CAS DataBase Reference1690-72-8(CAS DataBase Reference)
Safety Information
HS Code 2933399990
MSDS Information
Methyl 1-methylpiperidine-3-carboxylate Usage And Synthesis
UsesMethyl 1-methylpiperidine-3-carboxylate belongs to the class of organic compounds known as piperidinecarboxylic acids. Piperidinecarboxylic acids are compounds containing a piperidine ring with a carboxylic acid group. Methyl 1-methylpiperidine-3-carboxylate is a strong basic compound (based on its pKa). It could be used to synthesize (1-methylpiperidin-3-yl)methanol. The specific steps are shown as follows: into a 500 mL round bottom flask containing a solution of methyl 1-methylpiperidine-3- carboxylate (12.0 g, 76 mmol) in tetrahydrofuran (500 mL) was added lithium aluminumhydride (4.3 g, 114 mmol) in portions at 0 °C. The reaction mixture was stirred at room temperature for 1 h. The reaction was quenched with methanol at 0 °C, and the precipitated solid was filtered through celite. The filtrate was concentrated and the crude was purified by flash chromatography eluting with methanol in dichloromethane (5-10percent) to afford (1-methylpiperidin-3-yl)methanol as a solid.
Methyl 1-methylpiperidine-3-carboxylate Preparation Products And Raw materials
Preparation Products1-Methyl-3-piperidinemethanol
Tag:Methyl 1-methylpiperidine-3-carboxylate(1690-72-8) Related Product Information
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