Thiophen-2-carbonitril
Thiophen-2-carbonitril structure
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Common Name | Thiophen-2-carbonitril | ||
|---|---|---|---|---|
| CAS Number | 1003-31-2 | Molecular Weight | 109.149 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 193.0±13.0 °C at 760 mmHg | |
| Molecular Formula | C5H3NS | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 53.3±0.0 °C | |
| Symbol |
GHS02, GHS05, GHS07 |
Signal Word | Danger | |
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Synthesis of 2,2'-bipyrroles and 2,2'-thienylpyrroles from donor-acceptor cyclopropanes and 2-cyanoheteroles.
Org. Lett. 6(6) , 1057-9, (2004) [reaction: see text] Two new series of 2,2'-bipyrroles and 2,2'-thienylpyrroles have been prepared by trimethylsilyl trifluoromethanesulfonate (TMSOTf)-mediated reaction of donor-acceptor cyclopropanes with 2-cyanopyrroles and 2-cyanothiophene, respectively. ... |
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Understanding selectivity in the oxidative addition of the carbon-sulfur bonds of 2-cyanothiophene to Pt(0).
Inorg. Chem. 47(11) , 4596-604, (2008) The reaction of 2-cyanothiophene with a zerovalent platinum bisalkylphosphine fragment yields two thiaplatinacycles derived from the cleavage of the substituted and unsubstituted C-S bonds. While cleavage away from the cyano group is preferred kinetically, cl... |
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Introduction of double amidoxime group by double post surface modification on poly(vinylbenzyl chloride) beads for higher amounts of organic dyes, As (V) and Cr (VI) removal.
J. Colloid. Interface Sci. 470 , 39-46, (2016) In this study, the synthesis of micron-sized poly(vinylbenzyl chloride) (p(VBC)) beads and subsequent conversion of the reactive chloromethyl groups to double amidoxime group containing moieties by post modification is reported. The prepared beads were charac... |