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70201-42-2

3,5-Dibromopyridine-4-carbaldehyde

Catalog#: AR003484  |   CAS#: 70201-42-2  |   MDL#: MFCD06410681  |   MF: C6H3Br2NO  |   MW: 264.9021

Packsize Purity Price Availability Quantity
1g 98% $4.00 Global Stock Buy Now Add To Cart
5g 98% $7.00 Global Stock Buy Now Add To Cart
10g 98% $13.00 Global Stock Buy Now Add To Cart
25g 98% $33.00 Global Stock Buy Now Add To Cart
100g 98% $130.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003484
Chemical Name 3,5-Dibromopyridine-4-carbaldehyde
CAS Number 70201-42-2
Molecular Formula C6H3Br2NO
Molecular Weight 264.9021
MDL Number MFCD06410681
SMILES O=Cc1c(Br)cncc1Br

3,5-Dibromopyridine-4-carbaldehyde is a versatile compound commonly employed in chemical synthesis for its unique properties. In organic chemistry, this compound is utilized as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. Its selective reactivity at the aldehyde functional group enables the formation of complex molecular structures through a series of specific chemical reactions.One of the primary applications of 3,5-Dibromopyridine-4-carbaldehyde is in the synthesis of heterocyclic compounds. By utilizing its bromine substituents and aldehyde group, chemists can manipulate the molecule to undergo diverse transformations, leading to the construction of novel nitrogen-containing rings. These heterocycles play a crucial role in drug discovery and development, as they often exhibit significant biological activity.Additionally, 3,5-Dibromopyridine-4-carbaldehyde is employed in the preparation of ligands for metal-catalyzed reactions. The presence of the pyridine ring, coupled with the bromine atoms and aldehyde functionality, enables the compound to chelate transition metals effectively. This coordination chemistry aspect is crucial in catalyzing numerous organic transformations, enabling the synthesis of complex molecules with high efficiency and selectivity.Furthermore, this compound finds utility in material science for the fabrication of functionalized polymers and advanced materials. By incorporating 3,5-Dibromopyridine-4-carbaldehyde into polymer chains, researchers can impart specific properties, such as enhanced solubility or reactivity, to the resulting materials. These customized polymers have applications in various fields, including coatings, electronics, and biomedicine.In conclusion, the strategic utilization of 3,5-Dibromopyridine-4-carbaldehyde in chemical synthesis offers a wide array of possibilities for designing new molecules and materials with tailored properties and functionalities. Its versatility and reactivity make it a valuable building block for the creation of diverse compounds across different scientific disciplines.
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