10H-Phenothiazine,10-methyl-

Product Information

Molecular Formula:
C13H11 N S
Molecular Weight:
213.30
Description
Photoinitiator
Synonyms
N-METHYLPHENOTHIAZINE; 10-methyl-10h-phenothiazin; 10-Methyl-10H-phenothiazine; 9,10-Dibenzoisothiazine, 10-methyl-; Phenothiazide methyl derivative; Phenothiazine, 10-methyl-; AKOS 93806; 10-METHYLPHENOTHIAZINE
IUPAC Name
10-methylphenothiazine
Canonical SMILES
CN1C2=CC=CC=C2SC3=CC=CC=C31
InChI
InChI=1S/C13H11NS/c1-14-10-6-2-4-8-12(10)15-13-9-5-3-7-11(13)14/h2-9H,1H3
InChI Key
QXBUYALKJGBACG-UHFFFAOYSA-N
Melting Point
99-101 °C (lit.)
Flash Point
195.8 °F
Purity
98%
Density
1.207g/cm3

Safety Information

Hazards
H315 - H319 - H335
Precautionary Statement
P302 + P352 - P305 + P351 + P338

Computed Properties

XLogP3
4.2
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
0
Exact Mass
213.06122053 g/mol
Monoisotopic Mass
213.06122053 g/mol
Topological Polar Surface Area
28.5Ų
Heavy Atom Count
15
Formal Charge
0
Complexity
209
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113214178-A 3-aryl substituted anthranilic anhydride derivative and preparation method thereof 2021-05-28
CN-112479998-A Dihydroquinoline fluorescent probe and preparation method and application thereof 2020-11-16
CN-112479998-B Dihydroquinoline fluorescent probe and preparation method and application thereof 2020-11-16
CN-111939987-A Photocatalytic CO2Photocatalytic material for preparing synthetic gas by reduction and method thereof 2020-09-09
CN-111939987-B Photocatalytic CO2Photocatalytic material for preparing synthetic gas by reduction and method thereof 2020-09-09
JP-2021009392-A Optically anisotropic film 2020-09-08
WO-2022047394-A1 3d printed composites from phase separated materials 2020-08-31
WO-2022032236-A2 Polymeric composite membranes having oriented nanochannels and methods of making the same 2020-08-07
JP-2022024430-A Photo-curing composition for anticorrosion coating and its cured coating 2020-07-28
JP-2022024431-A Electrode foil for electrolytic capacitors and its manufacturing method 2020-07-28

Literatures

PMID Publication Date Title Journal
22940809 2012-11-01 Self sensitized photooxidation of N-methyl phenothiazine: acidity control of the competition between electron and energy transfer mechanisms Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology
21589550 2010-11-24 10H-Phenothia-zine 5-oxide Acta crystallographica. Section E, Structure reports online
18630266 2008-03-01 [Electrocatalytic oxidation of glutathione at 10-methylphenothiazine modified carbon paste electrode and its practical analytical application] Yao xue xue bao = Acta pharmaceutica Sinica
18075645 2008-01-07 Phenothiazine as a redox-active DNA base substitute: comparison with phenothiazine-modified uridine Organic & biomolecular chemistry
17595138 2007-07-20 The singlet oxygen oxidation of chlorpromazine and some phenothiazine derivatives. Products and reaction mechanisms The Journal of organic chemistry
17212410 2007-01-17 High energy and quantum efficiency in photoinduced charge separation Journal of the American Chemical Society
15970462 2006-02-01 Experimental and quantum chemical study on the vibrational spectroscopy of N-methylphenothiazines: part 1 Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
15962942 2005-06-01 Prediction of genotoxicity of chemical compounds by statistical learning methods Chemical research in toxicology
12929440 2003-01-21 Mechanism of the oxidation of aromatic sulfides catalysed by a water soluble iron porphyrin Organic & biomolecular chemistry
12489932 2002-12-26 Synthesis and characterization of pi-stacked phenothiazine-labeled oligodeoxynucleotides Organic letters
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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