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Home  > 3-(Bromomethyl)-2-methoxy-5-(trifluoromethyl)pyridine

AA24864

1227576-08-0 | 3-(Bromomethyl)-2-methoxy-5-(trifluoromethyl)pyridine

Packsize Purity Availability Price Discounted Price    Quantity
500mg 95% in stock $74.00 $52.00 -   +
1g 95% in stock $110.00 $77.00 -   +
5g 95% in stock $332.00 $232.00 -   +
10g 95% in stock $553.00 $388.00 -   +
25g 95% in stock $1,106.00 $775.00 -   +
50g 95% in stock $1,825.00 $1,278.00 -   +
100g 95% in stock $2,988.00 $2,092.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA24864
Chemical Name: 3-(Bromomethyl)-2-methoxy-5-(trifluoromethyl)pyridine
CAS Number: 1227576-08-0
Molecular Formula: C8H7BrF3NO
Molecular Weight: 270.0464896
MDL Number: MFCD16610204
SMILES: BrCc1cc(cnc1OC)C(F)(F)F

 

Upstream Synthesis Route
  • 3-(Bromomethyl)-2-methoxy-5-(trifluoromethyl)pyridine is a versatile compound that is frequently employed in chemical synthesis procedures. One key application of this compound is as a valuable building block for the synthesis of various biologically active compounds and pharmaceuticals. Its unique molecular structure, which incorporates both bromine and trifluoromethyl functional groups, allows for diverse reactivity in a range of synthetic transformations.In organic synthesis, 3-(Bromomethyl)-2-methoxy-5-(trifluoromethyl)pyridine can serve as a robust electrophilic reagent, participating in nucleophilic substitution reactions to introduce the pyridine moiety into complex molecular frameworks. The presence of the bromomethyl and trifluoromethyl groups imparts specific chemical properties that can be leveraged for selective functionalization of target molecules.Furthermore, this compound has found utility in transition metal-catalyzed cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds with high efficiency. By strategically incorporating 3-(Bromomethyl)-2-methoxy-5-(trifluoromethyl)pyridine into custom-designed synthetic routes, chemists can access structurally diverse compounds with tailored properties for applications in medicinal chemistry, materials science, and agrochemical research.
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