6-IODO-[1,2,4]TRIAZOLO[1,5,A]PYRIDINE
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![6-IODO-[1,2,4]TRIAZOLO[1,5,A]PYRIDINE structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220812/d9786cf58b014222ba0dc3968ba12682.png "6-IODO-[1,2,4]TRIAZOLO[1,5,A]PYRIDINE")
6-IODO-[1,2,4]TRIAZOLO[1,5,A]PYRIDINE
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CAS No:
614750-84-4
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Formula:
C6H4IN3
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Chemical Name:
6-IODO-[1,2,4]TRIAZOLO[1,5,A]PYRIDINE
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Synonyms:
6-Iodo-[1,2,4]triazolo[1,5-a]pyridine;6-Iodo-[1,2,4]Triazolo[1,5,A]Pyridine;6-iodo[1,2,4]triazolo[1,5-a]pyridine;6-Iodo-1,2,4-triazolo[1,5-a]pyridine;[1,2,4]Triazolo[1,5-a]pyridine,6-iodo-;PubChem17710;SCHEMBL1585961;CTK5B3294;DTXSID60590290;BCP26957
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CAS No:
6-IODO-[1,2,4]TRIAZOLO[1,5,A]PYRIDINE Basic Attributes
245.02
244.944977
1308068-626-2
DTXSID60590290
2933990090
6-IODO-[1,2,4]TRIAZOLO[1,5,A]PYRIDINE Use and Manufacturing
To a solution ofN'- (5-iodo-pyridin-2-yl)-N, N-dimethyl-formamidine in 8 ML of methanol was added 0. 84 mL (10. 4 mmol) pyridine and the resulting solution was cooled to 0 OC under nitrogen gas with stirring. To this solution was added 0. 66 gram (5. 9 mmol) HYDROXYLAMINE-O-SULFONIC acid to produce a pale yellow suspension. This suspension was allowed to warm to room temperature, then heated to reflux to give a yellow solution. After 16 hours, the solution was allowed to cool to room temperature, during which time crystals began to form. The mixture was cooled to 0 oC (ice bath) for two hours and the crystals were filtered off. After washing extensively with water, the crystals were air-dried to give 0. 74 g (3. 0 mmol, 67 percent) of the title compound as very fine, off-white needles ; 1H-NMR (300 MHz, CDC13, d) : 8. 88 (1H, s), 8. 28 (1H, s), 7. 71 (1H, dd, 1. 2 Hz, 9. 3 Hz), 7. 57 (1H, d, 9. 3 Hz) ; m/z : 246 [M+H] +.
Computed Properties
Molecular Weight:245.02
XLogP3:1.4
Hydrogen Bond Acceptor Count:2
Exact Mass:244.94499
Monoisotopic Mass:244.94499
Topological Polar Surface Area:30.2
Heavy Atom Count:10
Complexity:130
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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6-IODO-[1,2,4]TRIAZOLO[1,5,A]PYRIDINE
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