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Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 3,5-Dibromo-2-hydroxy-4-(trifluoromethyl)pyridine

AB63851

109919-34-8 | 3,5-Dibromo-2-hydroxy-4-(trifluoromethyl)pyridine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $105.00 $74.00 -   +
250mg 98% in stock $201.00 $141.00 -   +
1g 98% in stock $355.00 $248.00 -   +
5g 98% in stock $1,255.00 $879.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB63851
Chemical Name: 3,5-Dibromo-2-hydroxy-4-(trifluoromethyl)pyridine
CAS Number: 109919-34-8
Molecular Formula: C6H2Br2F3NO
Molecular Weight: 320.8894
MDL Number: MFCD11227186
SMILES: Brc1cnc(c(c1C(F)(F)F)Br)O

 

Computed Properties
Complexity: 318  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
XLogP3: 2  

 

 

Upstream Synthesis Route
  • 3,5-Dibromo-4-(trifluoromethyl)pyridin-2-ol is a versatile compound that finds wide application in chemical synthesis. This compound serves as a valuable building block for the preparation of various functionalized molecules due to its unique chemical properties.One key application of 3,5-Dibromo-4-(trifluoromethyl)pyridin-2-ol in chemical synthesis is as a starting material for the synthesis of pharmaceutical compounds. The presence of bromine and trifluoromethyl groups on the pyridine ring provides opportunities for further functionalization through various synthetic reactions. This allows for the introduction of specific functional groups required for the biological activity of the target molecule.Furthermore, the hydroxyl group on the pyridine ring can participate in hydrogen bonding interactions, making it useful for the design of molecular receptors or catalysts in organic synthesis. The presence of both electron-withdrawing and electron-donating groups in this compound enhances its reactivity and selectivity in synthetic transformations.Overall, 3,5-Dibromo-4-(trifluoromethyl)pyridin-2-ol serves as a valuable intermediate in complex organic synthesis, enabling the construction of diverse chemical structures with potential applications in pharmaceuticals, agrochemicals, and materials science.
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