CAS 1215787-31-7
:6-Bromo-4-chloropyrido[2,3-d]pyrimidine
Description:
6-Bromo-4-chloropyrido[2,3-d]pyrimidine is a heterocyclic compound characterized by its fused pyridine and pyrimidine rings, which contribute to its unique chemical properties. This compound features a bromine atom at the 6-position and a chlorine atom at the 4-position of the pyridine ring, influencing its reactivity and potential applications in medicinal chemistry. The presence of halogens can enhance the compound's biological activity and lipophilicity, making it a candidate for various pharmaceutical applications. Its structure allows for potential interactions with biological targets, which is of interest in drug design. Additionally, the compound may exhibit interesting electronic properties due to the conjugated system formed by the fused rings. As with many heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it versatile for synthetic applications. Overall, 6-Bromo-4-chloropyrido[2,3-d]pyrimidine is a significant compound in the field of organic and medicinal chemistry, warranting further investigation for its potential therapeutic uses.
Formula:C7H3BrClN3
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Found 4 products.
Pyrido[2,3-d]pyrimidine, 6-bromo-4-chloro-
CAS:Formula:C7H3BrClN3Purity:95%Color and Shape:SolidMolecular weight:244.47586-Bromo-4-chloropyrido[2,3-d]pyrimidine
CAS:<p>6-Bromo-4-chloropyrido[2,3-d]pyrimidine</p>Purity:95%Molecular weight:244.48g/mol6-Bromo-4-chloropyrido[2,3-d]pyrimidine
CAS:Formula:C7H3BrClN3Purity:95%Color and Shape:SolidMolecular weight:244.486-Bromo-4-chloropyrido[2,3-d]pyrimidine
CAS:<p>6-Bromo-4-chloropyrido[2,3-d]pyrimidine is a pyrimidine derivative that has been synthesized using cyclization and condensation techniques. The synthesis of this compound is efficient and uses relatively low amounts of starting materials. It can be made using microwave irradiation in a high yield. 6-Bromo-4-chloropyrido[2,3-d]pyrimidine is an aromatic ring with efficient methods for synthesis and bromination. This research could be used to produce new compounds with similar structures that are more potent than current drugs.</p>Purity:Min. 95%



