3,5-Diiodopyridine
CAS: 53710-18-2
Ref. 3D-FD156929
| 1g | To inquire | ||
| 2g | To inquire | ||
| 5g | To inquire | ||
| 250mg | To inquire | ||
| 500mg | To inquire |
Product Information
- 3,5-Dijod-pyridin
- 3,5-Diiodo-Pyridine
3,5-Diiodopyridine is a chemical compound that is not found in nature. It can be synthesized by the cross-coupling of 3,5-dibromopyridine with an organic halide. The reaction yields are dependent on the type of halide used in the experiment; for example, using bromine yields 3,5-diiodopyridine at a yield of 75%. This chemical was first synthesized and studied experimentally by G. Ciamician and A. Taddei in 1922. The functional theory suggests that this chemical reacts as a singlet due to its electron configuration (2s2p). Catalysis of the reaction occurs because it has been shown to be an effective catalyst for corticotropin-releasing factor receptor activation in pharmacokinetic studies. Cyanoacetylene is a molecule that is activated by 3,5-diiodopyridine during ring opening reactions to form indoles.
Chemical properties
Technical inquiry about: 3D-FD156929 3,5-Diiodopyridine
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