Application

Crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites¹

Reactant for synthesis of:
• Platinum chloro tetrazole complexes via azidation²
• Trans-stilbenes and cinnamates via Wittig olefination³
• Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment⁴
• Pentiptycenes for use as light-driven molecular brakes⁵

Reactant for formation of archipelago structures for formation of petroleum asphaltenes⁶

 性质

产品性状：本品溶于水，溶于氯仿,微溶于低分子量的脂肪族醇。热分解温度＞323℃，略带苄基味。与双酚AF配合用于氟橡胶的硫化剂。

1. S. Rooj, et al., Eur. Polymer J. 47, 1746-1755, (2011)

2. E. A. Popova, et al., Inorganica Chim. Acta 375, 242-247, (2011)

3. Amine- and sulfonamide-promoted wittig olefination reactions in water. J. McNulty and D. McLeod, Chem. Eur. J. 17, 8794-8798, (2011)

4. Orally active achiral N-hydroxyformamide inhibitors of ADAM-TS4 (aggrecanase-1) and ADAM-TS5 (aggrecanase-2) for the treatment of osteoarthritis. C. De Savi, et al., Bioorg. Med. Chem. Lett. 21, 3301-3306, (2011)

5. Pentiptycene-derived light-driven molecular brakes: substituent effects of the brake component. W. Sun, et al., Chem. Eur. J. 16, 11594-11604, (2010)

6. A. H. Alshareef, et al., Energy and Fuels 25, 2130-2136, (2011)

Beil. 16,IV,994

Fieser 5,30

Corp MSDS 1 (1), 405:B / FT-IR 2 (2), 3335:A / FT-IR 1 (2), 547:D / FT-NMR 1 (2), 1675:A / IR-Spectra (2), 1031:G / IR-Spectra (3), 1184:G / NMR-Reference 2 (2), 883:D / RegBook 1 (2), 2277:E / Structure Index 1, 356:D:5