5,6-Dibromothieno[2,3-d]pyrimidine


Chemical Name: 5,6-Dibromothieno[2,3-d]pyrimidine
CAS Number: 1841081-51-3
Product Number: AG00I1GD(AGN-PC-0WAMD6)
Synonyms:
MDL No:
Molecular Formula: C6H2Br2N2S
Molecular Weight: 293.9665

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



5,6-Dibromothieno[2,3-d]pyrimidine is a versatile building block in chemical synthesis, particularly in the field of organic chemistry. This compound is widely used as a key intermediate for the synthesis of various functional materials and pharmaceutical compounds. Its unique structure and reactivity make it an essential reagent for creating complex molecules with specific properties.In organic synthesis, 5,6-Dibromothieno[2,3-d]pyrimidine serves as a versatile substrate for various reactions such as cross-coupling reactions, nucleophilic substitution, and cycloaddition reactions. By functionalizing the bromine atoms at positions 5 and 6, chemists can introduce a wide range of functional groups or modify the core structure to tailor the properties of the final product.One of the key applications of 5,6-Dibromothieno[2,3-d]pyrimidine is in the synthesis of heterocyclic compounds, which are important in medicinal chemistry and materials science. By incorporating this building block into the molecular structure, researchers can design novel molecules with diverse biological activities or unique electronic properties.Furthermore, the presence of bromine atoms in 5,6-Dibromothieno[2,3-d]pyrimidine facilitates further derivatization, enabling the creation of more complex structures through sequential transformations. This compound plays a crucial role in the construction of multi-step synthesis pathways for the efficient production of target molecules with high purity and yield.In summary, 5,6-Dibromothieno[2,3-d]pyrimidine is a valuable tool in chemical synthesis, offering chemists a powerful means to access structurally diverse compounds for a wide range of applications, from drug discovery to materials development.