![]() 2,2,6,6-Tetramethylpiperidine structure
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Common Name | 2,2,6,6-Tetramethylpiperidine | ||
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CAS Number | 768-66-1 | Molecular Weight | 141.254 | |
Density | 0.8±0.1 g/cm3 | Boiling Point | 157.6±8.0 °C at 760 mmHg | |
Molecular Formula | C9H19N | Melting Point | -59°C | |
MSDS | Chinese USA | Flash Point | 24.4±0.0 °C | |
Symbol |
![]() ![]() GHS02, GHS06 |
Signal Word | Danger |
Nano-Drugs Based on Nano Sterically Stabilized Liposomes for the Treatment of Inflammatory Neurodegenerative Diseases.
PLoS ONE 10 , e0130442, (2015) The present study shows the advantages of liposome-based nano-drugs as a novel strategy of delivering active pharmaceutical ingredients for treatment of neurodegenerative diseases that involve neuroinflammation. We used the most common animal model for multip... |
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Oxidation of primary hydroxyl groups in chitooligomer by a laccase-TEMPO system and physico-chemical characterisation of oxidation products.
Carbohydr. Polym. 135 , 234-8, (2015) The aim of this study was to investigate the oxidation of chitooligomer by a laccase-TEMPO system which had not previously been examined. Chitooligomer was treated with laccase and TEMPO in order to evaluate the potential of a laccase-TEMPO system to improve ... |
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Reactivity of Amine/E(C6F5)3 (E = B, Al) Lewis Pairs toward Linear and Cyclic Acrylic Monomers: Hydrogenation vs. Polymerization.
Molecules 20 , 9575-90, (2015) This work reveals the contrasting reactivity of amine/E(C6F5)3 (E = B, Al) Lewis pairs toward linear and cyclic acrylic monomers, methyl methacrylate (MMA) and biorenewable γ-methyl-α-methylene-γ-butyrolactone (γMMBL). While mixing of 2,2,6,6-tetramethylpiper... |
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One-pot synthesis of 2,3-dihydro-pyrrolopyridinones using in situ generated formimines.
Org. Lett. 8 , 5889, (2006) A novel one-pot methodology is described for the synthesis of functionalized pyrrolopyridinones using in situ generated formimines and an ortho-lithiated pyridinecarboxamide species. Depending on the reaction conditions, this procedure allows versatile access... |
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