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AA02128

1003711-39-4 | 2-Bromo-5-cyano-6-picoline

Packsize Purity Availability Price Discounted Price    Quantity
1g 96% in stock $124.00 $87.00 -   +
5g 96% in stock $605.00 $423.00 -   +
10g 96% in stock $993.00 $695.00 -   +
25g 96% in stock $1,786.00 $1,250.00 -   +
100g 96% in stock $4,676.00 $3,273.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA02128
Chemical Name: 2-Bromo-5-cyano-6-picoline
CAS Number: 1003711-39-4
Molecular Formula: C7H5BrN2
Molecular Weight: 197.032
MDL Number: MFCD09839266
SMILES: Cc1nc(Br)ccc1C#N

 

Computed Properties
Complexity: 160  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 2  
XLogP3: 2  

 

 

Upstream Synthesis Route
  • 6-Bromo-2-methylnicotinonitrile is a versatile chemical compound that finds wide applications in chemical synthesis. It serves as a valuable building block in the preparation of various pharmaceutical and agrochemical products due to its unique structural properties. This compound acts as a key intermediate in the synthesis of diverse heterocyclic compounds, which are essential structural motifs in a range of biologically active molecules.The presence of the bromo group in 6-Bromo-2-methylnicotinonitrile enables it to partake in different types of chemical reactions such as nucleophilic substitution, Heck coupling, and Suzuki-Miyaura cross-coupling reactions. These reactions facilitate the modification and functionalization of the compound to generate novel derivatives with enhanced biological activities or tailored physicochemical properties.The introduction of the nitrile group in the molecule provides avenues for further derivatization through cyano group transformations, enabling the synthesis of a variety of functionalized compounds. Additionally, the presence of the methyl group at the 2-position of the nicotinonitrile ring imparts steric effects that influence the reactivity and selectivity of the compound in various synthetic transformations.Overall, 6-Bromo-2-methylnicotinonitrile serves as a valuable tool in the hands of synthetic chemists for the construction of complex molecular architectures with potential applications in the fields of pharmaceuticals, agrochemicals, and materials science.
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