AA51418
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 97% | in stock | $8.00 | $5.00 | - + | |
250mg | 97% | in stock | $13.00 | $9.00 | - + | |
1g | 97% | in stock | $23.00 | $17.00 | - + | |
5g | 97% | in stock | $62.00 | $43.00 | - + | |
10g | 97% | in stock | $115.00 | $80.00 | - + | |
25g | 97% | in stock | $245.00 | $171.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA51418 |
Chemical Name: | 5-Bromo-6-methylpicolinic acid |
CAS Number: | 137778-20-2 |
Molecular Formula: | C7H6BrNO2 |
Molecular Weight: | 216.032 |
MDL Number: | MFCD13181588 |
SMILES: | OC(=O)c1ccc(c(n1)C)Br |
To synthesize 5-Bromo-6-methylpicolinic acid, start with 6-methylpyridine-3-carboxaldehyde as the starting material. Perform a bromination reaction on the 5-position of the pyridine ring using N-bromosuccinimide (NBS) in the presence of a radical initiator like AIBN (azobisisobutyronitrile) under appropriate solvent conditions to obtain 5-bromo-6-methylpyridine-3-carboxaldehyde. Next, perform an oxidation reaction to convert the aldehyde group to a carboxylic acid. This can be achieved by using an oxidizing agent such as potassium permanganate (KMnO_4) in a neutral or slightly alkaline medium. This step transforms the aldehyde group into the corresponding carboxylic acid, yielding 5-bromo-6-methylpicolinic acid. Conditions like temperature and reaction time should be carefully controlled to ensure the selective oxidation of the aldehyde without over-oxidation of the methyl group on the pyridine ring. Ensure purification through recrystallization or chromatography to achieve the desired purity of 5-Bromo-6-methylpicolinic acid.