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61150-57-0

2-Bromo-4-fluorobenzylbromide

Catalog#: AR003HDA  |   CAS#: 61150-57-0  |   MDL#: MFCD03840524  |   MF: C7H5Br2F  |   MW: 267.9210

Packsize Purity Price Availability Quantity
1g 98% $4.00 Global Stock Buy Now Add To Cart
5g 98% $6.00 Global Stock Buy Now Add To Cart
10g 98% $12.00 Global Stock Buy Now Add To Cart
25g 98% $29.00 Global Stock Buy Now Add To Cart
100g 98% $113.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003HDA
Chemical Name 2-Bromo-4-fluorobenzylbromide
CAS Number 61150-57-0
Molecular Formula C7H5Br2F
Molecular Weight 267.9210
MDL Number MFCD03840524
SMILES BrCc1ccc(cc1Br)F

2-Bromo-4-fluorobenzylbromide, also known as $name$, is a versatile chemical compound widely utilized in organic synthesis for its unique properties and reactivity. This compound plays a crucial role in various chemical reactions and transformations, particularly in the field of pharmaceuticals and agrochemicals development.In chemical synthesis, 2-Bromo-4-fluorobenzylbromide serves as a valuable building block for the introduction of functional groups such as bromide and fluorine into organic molecules. Its reactivity allows for the selective substitution of hydrogen atoms in aromatic rings, leading to the formation of new carbon-carbon and carbon-heteroatom bonds. This enables the creation of structurally diverse compounds with enhanced biological activities and properties.One of the key applications of 2-Bromo-4-fluorobenzylbromide is in the synthesis of biologically active molecules, including pharmaceutical intermediates and natural product analogs. By incorporating this compound into the molecular structure, chemists can modify the physical and chemical properties of target compounds, improving their effectiveness and specificity in biological systems.Moreover, 2-Bromo-4-fluorobenzylbromide can be utilized in the preparation of ligands for transition metal-catalyzed cross-coupling reactions, enabling the efficient construction of complex organic molecules. Its compatibility with various reaction conditions and functional groups makes it a valuable tool for the synthesis of diverse chemical libraries and novel compounds with potential applications in drug discovery and material science.
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