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50841-50-4

2-Bromo-1-(3,5-dimethoxyphenyl)ethanone

Catalog#: AR00DD3Y  |   CAS#: 50841-50-4  |   MDL#: MFCD03425185  |   MF: C10H11BrO3  |   MW: 259.0965

Packsize Purity Price Availability Quantity
50mg 95% $101.00 2-3 weeks Buy Now Add To Cart
100mg 95% $137.00 2-3 weeks Buy Now Add To Cart
250mg 95% $184.00 2-3 weeks Buy Now Add To Cart
500mg 95% $276.00 2-3 weeks Buy Now Add To Cart
1g 95% $346.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00DD3Y
Chemical Name 2-Bromo-1-(3,5-dimethoxyphenyl)ethanone
CAS Number 50841-50-4
Molecular Formula C10H11BrO3
Molecular Weight 259.0965
MDL Number MFCD03425185
SMILES BrCC(=O)c1cc(OC)cc(c1)OC

2-BROMO-1-(3,5-DIMETHOXYPHENYL)ETHANONE is a versatile chemical compound widely used in organic synthesis due to its unique reactivity and functional groups. One of its primary applications is as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and other complex organic molecules.Specifically, the presence of the bromo group in 2-BROMO-1-(3,5-DIMETHOXYPHENYL)ETHANONE allows for selective functionalization reactions, enabling chemists to introduce new substituents or linkages at specific positions in a molecule. This bromo group can undergo diverse transformations such as nucleophilic substitution, Suzuki coupling, and Heck reactions, which are crucial in the construction of complex organic frameworks.Moreover, the ethanone moiety in 2-BROMO-1-(3,5-DIMETHOXYPHENYL)ETHANONE provides a handle for further modifications through traditional carbonyl chemistry, allowing for the incorporation of various functional groups or the formation of cyclic structures. This flexibility in derivatization makes it a valuable intermediate in the synthesis of bioactive compounds and fine chemicals.Overall, the strategic placement of functional groups in 2-BROMO-1-(3,5-DIMETHOXYPHENYL)ETHANONE makes it a valuable tool in modern chemical synthesis, enabling chemists to access structurally diverse and pharmaceutically relevant molecules through efficient and controlled reactions.
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