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AA51418

137778-20-2 | 5-Bromo-6-methylpicolinic acid

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 -   +

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*All prices are in USD.

Description
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

 

Upstream Synthesis Route
  • 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.
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