| Weight | 181.285 g/mol |
|---|---|
| Formula | C8H7NS2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
2-(Methylthio)benzothiazole
64036-43-7, 31621-01-9, 615-22-5
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- A convenient synthesis of 3-cyano-4-imino-2-methylthio-4H-pyrimido [2,1-b] [1,3] benzothiazole and its reactions with selected nucleophiles (Arkivoc, 2006)
- Transition metal-modified polyoxometalates supported on carbon as catalyst in 2-(methylthio)-benzothiazole sulfoxidation (Journal of Chemical Sciences, 2015)
- SYNTHESIS AND IN VITRO ANTICANCER ACTIVITY OF 8-CHLORO-3-CYANO-4-IMINO-2-METHYLTHIO-4H-PYRIMIDO [2, 1-B] [1, 3] BENZOTHIAZOLE AND ITS 2-SUBSTITUTED DERIVATIVES (Asian Journal of Pharmaceutical Research and Health Care, 2010)
- A Convenient Synthesis Of 2-Methyl-5-(Methylthio)Benzothiazole (Synthetic Communications, 1997)
- Bis[4-(methylthio)phenylmethyleneaminophenyl] disulfide, 2-[4-(methylthio)phenyl]-2,3-dihydro-1,3-benzothiazole, and its nickel(II) and cobalt(II) complexes: Synthesis, adsorption on gold surface and electrochemical characterization (Journal of Sulfur Chemistry, 2007)
- Synthesis and in-vitro anticancer activity of 3-cyano-6,9-dimethyl-4-imino 2-methylthio 4H-pyrimido [2,1-b] [1,3] benzothiazole and its 2-substituted derivatives (Journal of Pharmacy Research, 2013)
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SMILESCSC1=NC2=CC=CC=C2S1
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2-(Methylthio)benzothiazole
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