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| | 4-N-Boc-4-N-Methyl-aminopiperidine Basic information |
| Product Name: | 4-N-Boc-4-N-Methyl-aminopiperidine | | Synonyms: | 4-(Methylamino)piperidine, 4-BOC protected;N-Methyl-N-(piperidin-1-yl)(tert-butoxy)forMaMide;tert-Butyl Methyl(4-piperidyl)carbamate;tert-Butyl methyl(piperidin-4-yl)carbamate, 4-[(tert-Butyoxycarbonyl)(methyl)amino]piperidine;4-N-Boc-4-(MethylaMino)piperidine;Carbamic acid, N-methyl-N-4-piperidinyl-, 1,1-dimethylethyl ester;tert-Butyl Methyl(4-piperidyl)carbamate;tert-butyl n-methyl-n-(4-piperidyl)carbamate | | CAS: | 108612-54-0 | | MF: | C11H22N2O2 | | MW: | 214.3 | | EINECS: | 672-392-7 | | Product Categories: | Piperidine | | Mol File: | 108612-54-0.mol |  |
| | 4-N-Boc-4-N-Methyl-aminopiperidine Chemical Properties |
| Melting point | 50°C(lit.) | | Boiling point | 287.9±29.0 °C(Predicted) | | density | 1.01±0.1 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | form | crystalline powder | | pka | 10.05±0.10(Predicted) | | color | White | | CAS DataBase Reference | 108612-54-0(CAS DataBase Reference) |
| | 4-N-Boc-4-N-Methyl-aminopiperidine Usage And Synthesis |
| Uses |
4-N-Boc-4-N-methyl-aminopiperidine, or Tert-butyl methyl(piperidin-4-yl)carbamate (TBMPC) is a derivative of piperidine and is structurally similar to other carbamates. It inhibits the enzyme cyclooxygenase and modulates the activity of the neurotransmitter GABA. This compound has demonstrated anticonvulsant and anti-inflammatory activity. TBMPC has been studied for its potential use in various in vivo and in vitro applications. It has been reported to reduce the frequency and duration of seizures in animal models and reduce the production of pro-inflammatory cytokines in cell culture.
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| | 4-N-Boc-4-N-Methyl-aminopiperidine Preparation Products And Raw materials |
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