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Quality Level
Assay
97%
mp
88-95 °C (lit.)
functional group
bromo
SMILES string
Cc1cc(Br)cnc1N
InChI
1S/C6H7BrN2/c1-4-2-5(7)3-9-6(4)8/h2-3H,1H3,(H2,8,9)
InChI key
KBLGGRWUEVCNPY-UHFFFAOYSA-N
General description
2-Amino-5-bromo-3-methylpyridine can be prepared from 2-amino-3-methylpyridine, via bromination.
Application
2-Amino-5-bromo-3-methylpyridine may be used to synthesize:
- 5-bromo-2-chloro-3-methylpyridine
- 2-azidopyridine 1-oxide
- 2-amino-5-bromo-3-methylpyridine 1-oxide
- 2,5-dibromo-3-methyl pyridine
- ethyl-3,6-dibromo-8-methylimidazo[1,2-a]pyridine-2-carboxylate
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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2, 5-and 5, 6-Dihalonicotinic acids and their precursors.
Journal of Chemical and Engineering Data, 15(4), 590-591 (1970)
Ring contraction of 2-azidopyridine 1-oxides and related compounds. 2-Cyano-1-hydroxypyrroles and-imidazoles.
Journal of the American Chemical Society, 98(6), 1478-1486 (1976)
Microwave-Assisted One-Pot Synthesis of Substituted 3-Bromoimidazo [1, 2-a] pyridines and Imidazoheterocycles.
Journal of Heterocyclic Chemistry, 51(5), 1509-1515 (2014)
Synthesis of the grass alkaloid perlolidine through a pyridyne cyclisation reaction.
Indian J. Chem. B, 40(11), 1129-1131 (2001)
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