CAS 72832-23-6
:ethyl 3-bromothieno[2,3-b]pyridine-2-carboxylate
Description:
Ethyl 3-bromothieno[2,3-b]pyridine-2-carboxylate is a chemical compound characterized by its unique structure, which combines a thieno[2,3-b]pyridine ring system with a carboxylate ester functional group. This compound features a bromine atom at the 3-position of the thieno ring, which can influence its reactivity and biological activity. The ethyl ester group contributes to its solubility and potential applications in organic synthesis and medicinal chemistry. The presence of both heteroatoms (sulfur and nitrogen) in the ring structure may impart interesting electronic properties and reactivity patterns. Ethyl 3-bromothieno[2,3-b]pyridine-2-carboxylate may be utilized in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in the synthesis of more complex molecules. Additionally, compounds with similar structures have been investigated for their potential pharmacological activities, including antimicrobial and anticancer properties. As with any chemical substance, proper handling and safety precautions should be observed due to its potential hazards.
Formula:C10H8BrNO2S
InChI:InChI=1/C10H8BrNO2S/c1-2-14-10(13)8-7(11)6-4-3-5-12-9(6)15-8/h3-5H,2H2,1H3
SMILES:CCOC(=O)c1c(c2cccnc2s1)Br
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Found 4 products.
Ethyl 3-bromothieno[2,3-b]pyridine-2-carboxylate
CAS:Formula:C10H8BrNO2SPurity:98%Molecular weight:286.14503-Bromo-thieno[2,3-b]pyridine-2-carboxylic acid ethyl ester
CAS:<p>3-Bromo-thieno[2,3-b]pyridine-2-carboxylic acid ethyl ester</p>Purity:95%Molecular weight:286.148g/mol3-Bromo-thieno[2,3-b]pyridine-2-carboxylic acid ethyl ester
CAS:Formula:C10H8BrNO2SPurity:98%Color and Shape:SolidMolecular weight:286.14ethyl 3-bromothieno[2,3-b]pyridine-2-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H8BrNO2SPurity:Min. 95%Molecular weight:286.14 g/mol



