2-Sulfanylphenol
2-Sulfanylphenol structure
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Common Name | 2-Sulfanylphenol | ||
|---|---|---|---|---|
| CAS Number | 1121-24-0 | Molecular Weight | 126.176 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 223.7±23.0 °C at 760 mmHg | |
| Molecular Formula | C6H6OS | Melting Point | 20 °C | |
| MSDS | Chinese USA | Flash Point | 89.1±22.6 °C | |
| Symbol |
GHS05, GHS06 |
Signal Word | Danger | |
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ZEB2 drives immature T-cell lymphoblastic leukaemia development via enhanced tumour-initiating potential and IL-7 receptor signalling.
Nat. Commun. 6 , 5794, (2015) Early T-cell precursor leukaemia (ETP-ALL) is a high-risk subtype of human leukaemia that is poorly understood at the molecular level. Here we report translocations targeting the zinc finger E-box-binding transcription factor ZEB2 as a recurrent genetic lesio... |
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Speciation analysis of mercury in sediments, zoobenthos and river water samples by high-performance liquid chromatography hyphenated to atomic fluorescence spectrometry following preconcentration by solid phase extraction.
Anal. Chim. Acta 615(2) , 115-23, (2008) A high-pressure microwave digestion was applied for microwave-assisted extraction (MAE) of mercury species from sediments and zoobenthos samples. A mixture containing 3molL(-1) HCl, 50% aqueous methanol and 0.2molL(-1) citric acid (for masking co-extracted Fe... |
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Vanadium(IV) Complexes with Mixed O,S Donor Ligands. Syntheses, Structures, and Properties of the Anions Tris(2-mercapto-4-methylphenolato)vanadate(IV) and Bis(2-mercaptophenolato)oxovanadate(IV).
Inorg. Chem. 35(2) , 347-356, (1996) Reaction of VO(acac)(2) with 2-mercaptophenol (mpH(2)) in the presence of triethylamine gives the mononuclear tris complex (Et(3)NH)(2)[V(mp)(3)] (1), in which the vanadyl oxygen has been displaced. An analogous reaction using 2-mercapto-4-methylphenol (mmpH(... |
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Palladium complexes with simultaneous O: S coordination, syntheses, structures and characterization of complexes with 2-mercaptophenol or 2-mercaptopyridine N-oxide. Shi J-C, et al.
Polyhedron 16(3) , 369-75, (1997)
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Benzodiazepine Analogues. Part 15.1 Synthesis of Benzoxathiepine Derivatives. Gelebe AC and Kaye PT.
Synth. Commun. 29 , 4459-4475, (1996)
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