3,5-di(trifluoromethyl)phenyl isothiocyanate
3,5-di(trifluoromethyl)phenyl isothiocyanate structure
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Common Name | 3,5-di(trifluoromethyl)phenyl isothiocyanate | ||
|---|---|---|---|---|
| CAS Number | 23165-29-9 | Molecular Weight | 271.182 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 227.5±40.0 °C at 760 mmHg | |
| Molecular Formula | C9H3F6NS | Melting Point | 160ºC | |
| MSDS | Chinese USA | Flash Point | 91.4±27.3 °C | |
| Symbol |
GHS06 |
Signal Word | Danger | |
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Synthesis of chiral sulfoximine-based thioureas and their application in asymmetric organocatalysis.
Beilstein J. Org. Chem. 8 , 1443-51, (2012) For the first time, chiral sulfoximine derivatives have been applied as asymmetric organocatalysts. In combination with a thiourea-type backbone the sulfonimidoyl moiety leads to organocatalysts showing good reactivity in the catalytic desymmetrization of a c... |
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Self-assembled monolayers of aromatic omega-aminothiols on gold: surface chemistry and reactivity.
Langmuir 26(6) , 3949-54, (2010) Amino-terminated self-assembled monolayers on gold substrates were studied by X-ray photoelectron spectroscopy (XPS), near-edge X-ray absorption fine structure (NEXAFS) measurements, and atomic force microscopy (AFM). Two different omega-amino-4,4'-terphenyl ... |
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Determination of accessible amino groups on surfaces by chemical derivatization with 3,5-bis(trifluoromethyl)phenyl isothiocyanate and XPS/NEXAFS analysis.
Anal. Bioanal. Chem 396(2) , 725-38, (2010) The determination of amino groups on surfaces capable of binding biomolecules is important for the understanding and optimization of technologically relevant coupling processes. In this study, three different types of amino-functionalized model surfaces, amin... |
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Highly diastereo-and enantioselective direct aldol reactions promoted by water-compatible organocatalysts bearing a pyrrolidinyl-camphor structural scaffold. Tzeng Z-H, et al.
Tetrahedron 65(5) , 2879-2888, (2009)
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