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72459-46-2

1-(4-Bromobenzyl)-1H-imidazole

Catalog#: AR00FCIQ  |   CAS#: 72459-46-2  |   MDL#: MFCD06421442  |   MF: C10H9BrN2  |   MW: 237.0959

Packsize Purity Price Availability Quantity
100mg 98% $6.00 Global Stock Buy Now Add To Cart
250mg 98% $8.00 Global Stock Buy Now Add To Cart
1g 98% $19.00 Global Stock Buy Now Add To Cart
5g 98% $66.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00FCIQ
Chemical Name 1-(4-Bromobenzyl)-1H-imidazole
CAS Number 72459-46-2
Molecular Formula C10H9BrN2
Molecular Weight 237.0959
MDL Number MFCD06421442
SMILES Brc1ccc(cc1)Cn1cncc1

1-(4-Bromobenzyl)-1H-imidazole is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the creation of various organic molecules, particularly in the field of drug discovery and medicinal chemistry. With its substituted benzene ring and imidazole core, 1-(4-Bromobenzyl)-1H-imidazole offers a convenient platform for introducing functional groups and creating structurally diverse compounds.In chemical synthesis, 1-(4-Bromobenzyl)-1H-imidazole acts as a crucial intermediate in the preparation of biologically active compounds, such as pharmaceuticals, agrochemicals, and materials. Its presence enables the introduction of the 4-bromobenzyl group into target molecules, which can significantly influence their physical and chemical properties. By incorporating 1-(4-Bromobenzyl)-1H-imidazole into synthetic routes, chemists can control the regioselectivity and stereochemistry of the final product, leading to tailored solutions for specific applications.Furthermore, the reactivity of 1-(4-Bromobenzyl)-1H-imidazole allows for versatile transformations, including cross-coupling reactions, nucleophilic substitutions, and metal-catalyzed processes. These reactions enhance the synthetic accessibility of complex molecules and facilitate the exploration of new chemical space. By harnessing the potential of 1-(4-Bromobenzyl)-1H-imidazole in chemical synthesis, researchers can expand their toolkit for designing novel compounds with desired biological activities and physicochemical properties.
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