5-BROMO-IMIDAZO[1,2-A]PYRIDINE
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![5-BROMO-IMIDAZO[1,2-A]PYRIDINE structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220811/2e49fac00af845bd9772d214ec18a14e.png "5-BROMO-IMIDAZO[1,2-A]PYRIDINE")
5-BROMO-IMIDAZO[1,2-A]PYRIDINE
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CAS No:
69214-09-1
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Formula:
C7H5BrN2
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Chemical Name:
5-BROMO-IMIDAZO[1,2-A]PYRIDINE
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Synonyms:
5-BROMO-IMIDAZO[1,2-A]PYRIDINE;5-BROMOIMIDAZO[1,2-A]PYRIDINE, 95+%;5-bromoH-imidazo[1,2-a]pyridine;5-BROMO-5H-IMIDAZO[2,1-B][1,3]OXAZINE;5-Bromo-1,5-dihydroimidazo[1,2-a]pyridine
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CAS No:
Safety Information
NONH for all modes of transport
3
|Warning|H302 (20%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 5 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
5-BROMO-IMIDAZO[1,2-A]PYRIDINE Use and Manufacturing
PREPARATION 8; 5-Bromoimidazo [1, 2-a] pyridine Add 2-bromo-I, l-diethoxyethane (3.64 g, 18.48 mmol) to a solution of 6- bromopyridin-2-ylamine (l. Og, 5.77 mmol) in n-butanol (40 ml). Reflux overnight and cool. Filtration of the reaction mixture gives 1.3 g (81percent) of 5-bromoimidazo [1, 2- pyridine hydrobromide as a white solid. ESMS (M++1) : 198.9 m/z. Add saturated sodium bicarbonate (300 ml) to a suspension of 5- bromoimidazo [1, 2-a] pyridine hydrobromide (13. 0g, 46.96 mmol) in ethyl acetate. Separate the organic layer, wash with saturated sodium bicarbonate, dry over magnesium sulfate, and concentrate under reduced pressure to give 9.7 g (100percent) of the title compound as a white solid.Method 32
Computed Properties
Molecular Weight:197.03
XLogP3:2.8
Hydrogen Bond Acceptor Count:1
Exact Mass:195.96361
Monoisotopic Mass:195.96361
Topological Polar Surface Area:17.3
Heavy Atom Count:10
Complexity:129
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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