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1637-16-7 | 10H-Phenothiazine, 10-ethyl-
CAS No: 1637-16-7 Catalog No: AG001UBK MDL No:
Product Description
Catalog Number:
AG001UBK
Chemical Name:
10H-Phenothiazine, 10-ethyl-
CAS Number:
1637-16-7
Molecular Formula:
C14H13NS
Molecular Weight:
227.3247
IUPAC Name:
10-ethylphenothiazine
InChI:
InChI=1S/C14H13NS/c1-2-15-11-7-3-5-9-13(11)16-14-10-6-4-8-12(14)15/h3-10H,2H2,1H3
InChI Key:
IQZBMUCMEBSKSS-UHFFFAOYSA-N
SMILES:
CCN1c2ccccc2Sc2c1cccc2
NSC Number:
121
Properties
Complexity:
221
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
227.077g/mol
Formal Charge:
0
Heavy Atom Count:
16
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
227.325g/mol
Monoisotopic Mass:
227.077g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
28.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.5
Literature
| Title | Journal |
|---|---|
| 10-Ethyl-10H-phenothia-zine-3-carbaldehyde. | Acta crystallographica. Section E, Structure reports online 20111201 |
| Synthesis, crystal structures, photophysical properties, and bioimaging of living cells of bis-β-diketonate phenothiazine ligands and its cyclic dinuclear complexes. | Inorganic chemistry 20110905 |
| The singlet oxygen oxidation of chlorpromazine and some phenothiazine derivatives. Products and reaction mechanisms. | The Journal of organic chemistry 20070720 |
| Horseradish peroxidase-catalyzed polymerization of cardanol in the presence of redox mediators. | Biomacromolecules 20040101 |
| Synthesis and biological activity of N-acylphenothiazines. | International journal of antimicrobial agents 20000401 |
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