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assay
98%
form
solid
bp
95-96 °C/12.5 mmHg (lit.)
mp
41-43 °C (lit.)
functional group
bromo
SMILES string
Cc1ccc(Br)nc1
InChI
1S/C6H6BrN/c1-5-2-3-6(7)8-4-5/h2-4H,1H3
InChI key
YWNJQQNBJQUKME-UHFFFAOYSA-N
Application
2-Bromo-5-methylpyridine has been used as starting reagent for the synthesis of:
- 5,5′-dimethyl-2,2′-bipyridine
- 5-methyl-2,2′:6′,2″-terpyridine
- 5-bromo-5″-methyl-2,2′:6′,2″-terpyridine
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
217.4 °F - closed cup
flash_point_c
103 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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High yield synthesis of 5, 5'-dimethyl-2, 2'-bipyridine and 5, 5 ?-dimethyl-2, 2': 6', 2 ?-terpyridine and some bisfunctionalization reactions using N-bromosuccinimide.
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A series of air-stable spiro-fused ladder-type boron(III) compounds has been designed, synthesized, and the electrochemistry and photophysical behavior have been characterized. By simply varying the substituents on the pyridine ring and extending the π-conjugation of the spiro framework, the emission
Synthesis of two covalently linked bis (2, 2': 6', 2''-terpyridine)(terpy) chelating ligands with different length spacers, comparison of the crystal structures of their mononuclear nickel (II) complexes, and kinetic and mechanistic studies of the reaction of one ligand with [Fe (terpy) 2] 2+.
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