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AA64829

14659-58-6 | 2-Bromo-5-fluoro-m-xylene

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $7.00 $5.00 -   +
5g 98% in stock $21.00 $15.00 -   +
10g 98% in stock $34.00 $24.00 -   +
25g 98% in stock $69.00 $48.00 -   +
100g 98% in stock $271.00 $190.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA64829
Chemical Name: 2-Bromo-5-fluoro-m-xylene
CAS Number: 14659-58-6
Molecular Formula: C8H8BrF
Molecular Weight: 203.0515
MDL Number: MFCD09864702
SMILES: Fc1cc(C)c(c(c1)C)Br

 

Computed Properties
Complexity: 104  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 1  
XLogP3: 4.2  

 

 

Upstream Synthesis Route
  • 2-Bromo-5-fluoro-1,3-dimethylbenzene, also known as bromofluorodimethylbenzene, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the preparation of various organic molecules through functional group transformations. One common application of 2-Bromo-5-fluoro-1,3-dimethylbenzene is in the synthesis of pharmaceuticals, agrochemicals, and materials science.In organic chemistry, 2-Bromo-5-fluoro-1,3-dimethylbenzene can undergo substitution reactions to introduce additional functional groups at the bromo or fluoro position. These reactions allow chemists to modify the structure of the molecule, creating new derivatives with distinct properties. Furthermore, the bromine and fluorine atoms in the compound can act as regioselective and stereoselective handles for further elaboration, enabling the synthesis of complex molecules.Additionally, 2-Bromo-5-fluoro-1,3-dimethylbenzene can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling or Heck coupling, to form carbon-carbon bonds with other organic substrates. This versatility makes it a valuable tool for connecting different fragments in the synthesis of pharmaceutical intermediates or fine chemicals.Overall, the unique structure of 2-Bromo-5-fluoro-1,3-dimethylbenzene offers a wide range of opportunities for chemists to explore its reactivity and utility in various synthetic applications.
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