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Wichtige Dokumente
425346
10-Methylphenothiazin
98%
Synonym(e):
10-Methyl-10H -phenothiazine, N -Methylphenothiazine
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About This Item
Empirische Formel (Hill-System):
C13H11NS
CAS-Nummer:
Molekulargewicht:
213.30
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12162002
PubChem Substanz-ID:
NACRES:
NA.23
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Assay
98%
mp (Schmelzpunkt)
99-101 °C (lit.)
SMILES String
CN1c2ccccc2Sc3ccccc13
InChI
1S/C13H11NS/c1-14-10-6-2-4-8-12(10)15-13-9-5-3-7-11(13)14/h2-9H,1H3
InChIKey
QXBUYALKJGBACG-UHFFFAOYSA-N
Verwandte Kategorien
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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Phenothiazine as a redox-active DNA base substitute: comparison with phenothiazine-modified uridine.
Clemens Wagner et al.
Organic & biomolecular chemistry, 6(1), 48-50 (2007-12-14)
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 phenothiazine-modified uridine has different optical and electrochemical
G Bidan et al.
Biosensors & bioelectronics, 10(1-2), 219-229 (1995-01-01)
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/delivering is based on host-guest interaction.
Henrietta Endrédi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 63(2), 349-360 (2005-06-23)
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 the vibrational spectroscopic behaviour of the phenothiazine skeleton and dealt with the aldehyde and
S A Nadeem Hashmi et al.
Organic letters, 4(26), 4571-4574 (2002-12-20)
[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 solid-phase synthesizer. Phenothiazine-labeled oligodeoxynucleotides form
Li Bai et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 43(3), 291-294 (2008-07-17)
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 paste electrode (CPE), the response could be
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