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ChemicalBook--->CAS DataBase List--->1211515-68-2

1211515-68-2

1211515-68-2 Structure

1211515-68-2 Structure
IdentificationBack Directory
[Name]

3-Bromo-5-methylpyridine-2-carboxylic acid
[CAS]

1211515-68-2
[Synonyms]

3-Bromo-5-methylpicolinicaci
3-BroMo-5-Methylpicolinic acid
3-broMo-5-Methylpyridin-2-carboxylic acid
3-Bromo-5-methylpyridine-2-carboxylic acid
3-bromo-5-methyl-2-pyridinecarboxylic acid
2-Pyridinecarboxylic acid, 3-bromo-5-methyl-
3-Bromo-5-methylpyridine-2-carboxylic acid 97%
3-Bromo-5-methylpicolinic acid, 3-Bromo-2-carboxy-5-methylpyridine
[Molecular Formula]

C7H6BrNO2
[MDL Number]

MFCD17214206
[MOL File]

1211515-68-2.mol
[Molecular Weight]

216.03
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

solid
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P271-P260-P280
[RIDADR ]

UN2811
[HS Code ]

2933399990
Hazard InformationBack Directory
[Description]

3-Bromo-5-methylpyridine-2-carboxylic acid is an organic compound with the molecular formula C7H6BrNO2. It is a derivative of pyridine, a primary heterocyclic organic compound. This compound is characterized by a bromine atom at the third position, a methyl group at the fifth position, and a carboxylic acid group at the second position of the pyridine ring. 3-Bromo-5-methylpyridine-2-carboxylic acid can be synthesized through several methods. One common method involves the bromination of 5-methylpyridine-2-carboxylic acid using a brominating agent such as N-bromosuccinimide (NBS) in the presence of a catalyst like azobisisobutyronitrile (AIBN). The reaction typically occurs in an organic solvent such as dichloromethane at a controlled temperature.
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