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Home > Products> 749927-80-8
749927-80-8

4-Bromo-2-fluoro-N,N-dimethylbenzamide

Catalog#: AR005SDX  |   CAS#: 749927-80-8  |   MDL#: MFCD09878360  |   MF: C9H9BrFNO  |   MW: 246.0763

Packsize Purity Price Availability Quantity
100mg 98% $14.00 Global Stock Buy Now Add To Cart
250mg 98% $23.00 Global Stock Buy Now Add To Cart
1g 98% $55.00 Global Stock Buy Now Add To Cart
5g 98% $170.00 Global Stock Buy Now Add To Cart
25g 98% $667.00 Global Stock Buy Now Add To Cart
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Catalog Number AR005SDX
Chemical Name 4-Bromo-2-fluoro-N,N-dimethylbenzamide
CAS Number 749927-80-8
Molecular Formula C9H9BrFNO
Molecular Weight 246.0763
MDL Number MFCD09878360
SMILES O=C(N(C)C)C1=CC=C(Br)C=C1F

4-Bromo-2-fluoro-N,N-dimethylbenzamide is a valuable chemical compound commonly used in chemical synthesis applications. This versatile compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactive properties make it an essential building block for designing and synthesizing complex organic molecules with specific biological or industrial functions.In chemical synthesis, 4-Bromo-2-fluoro-N,N-dimethylbenzamide plays a crucial role in introducing both bromine and fluorine functional groups into target molecules. These substituents can significantly alter the physicochemical properties and biological activities of the final compounds. Additionally, the dimethylbenzamide moiety provides a stable and versatile scaffold for further modifications, allowing for the fine-tuning of molecular properties.Researchers and chemists utilize 4-Bromo-2-fluoro-N,N-dimethylbenzamide in various synthetic pathways to construct diverse organic frameworks, such as heterocycles, amino acid derivatives, and natural product analogs. Its strategic incorporation in multistep syntheses enables the selective introduction of specific functional groups at pre-defined positions, facilitating the efficient assembly of complex molecular structures with high purity and yield.Moreover, the reactivity of 4-Bromo-2-fluoro-N,N-dimethylbenzamide under various reaction conditions enables the formation of key intermediates and precursors for further elaboration. Its compatibility with common synthetic methods, such as cross-coupling reactions, nucleophilic substitutions, and transition metal-catalyzed transformations, broadens its utility in diverse synthetic strategies aimed at achieving molecular diversity and complexity.Overall, 4-Bromo-2-fluoro-N,N-dimethylbenzamide serves as a versatile and indispensable tool in chemical synthesis, empowering chemists to design and access novel compounds with tailored properties for applications in drug discovery, material science, and chemical research.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302-H312-H332
Precautionary Statements P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P403+P233-P501
Class -
Packing Group -

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