n-methylphenothiazine
n-methylphenothiazine structure
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Common Name | n-methylphenothiazine | ||
|---|---|---|---|---|
| CAS Number | 1207-72-3 | Molecular Weight | 213.298 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 341.6±12.0 °C at 760 mmHg | |
| Molecular Formula | C13H11NS | Melting Point | 99-101 °C(lit.) | |
| MSDS | USA | Flash Point | 160.4±19.6 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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[Electrocatalytic oxidation of glutathione at 10-methylphenothiazine modified carbon paste electrode and its practical analytical application].
Yao Xue Xue Bao 43(3) , 291-4, (2008) The electrocatalytic oxidation of glutathione (reduced form GSH) at 10-methylphenothiazine (MPT) modified carbon paste electrode (MPT/CPE) was investigated by cyclic voltammetry (CV). Although GSH itself showed a very poor electrochemical response at carbon p... |
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Phenothiazine as a redox-active DNA base substitute: comparison with phenothiazine-modified uridine.
Org. Biomol. Chem. 6(1) , 48-50, (2008) Phenothiazine can be incorporated as a redox-active probe into DNA in two conceptually different ways: the non-nucleosidic DNA base surrogate exhibits similar properties to 10-methylphenothiazine but with no preferential base-pairing properties, whereas the p... |
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Incorporation of sulphonated cyclodextrins into polypyrrole: an approach for the electro-controlled delivering of neutral drugs.
Biosens. Bioelectron. 10(1-2) , 219-29, (1995) The electro-controlled delivery of drugs based on the doping-dedoping mechanism of Electro-Conducting Polymers is restricted to charged substances acting as dopants. In order to overcome this limitation, this study presents an approach where the trapping/deli... |
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Synthesis and characterization of pi-stacked phenothiazine-labeled oligodeoxynucleotides.
Org. Lett. 4(26) , 4571-4, (2002) [reaction: see text] A facile procedure for the incorporation of N-methyl phenothiazine as the terminal nucleoside in oligodeoxynucleotides is reported. The phenothiazine nucleoside analogue is synthesized and then incorporated into DNA using an automated DNA... |
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[Oxidation of phenothiazine and its N-methyl derivative by the combination of iodobenzene and vanadium acetylacetonate].
Pharmazie 40(3) , 202-3, (1985)
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Experimental and quantum chemical study on the vibrational spectroscopy of N-methylphenothiazines: part 1.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 63(2) , 349-60, (2006) In this work the authors deal with the vibrational spectroscopy of three derivatives of phenothiazine: the 10-methyl-10H-phenothiazine, the 10 methyl-10H-phenothiazine-3-carbaldehyde and the 10-methyl-10H-phenothiazine-3-yl-methanol. The authors investigated ... |