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Assay
98%
form
solid
bp
95-96 °C/12.5 mmHg (lit.)
mp
41-43 °C (lit.)
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
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)
217.4 °F - closed cup
Flash Point(C)
103 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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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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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+.
J. Chem. Soc., Dalton Trans., 4, 445-449 (2000)
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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
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