CAS 1234616-31-9

Ethyl 3-amino-5-bromothieno[2,3-b]pyridine-2-carboxylate

Description:

Ethyl 3-amino-5-bromothieno[2,3-b]pyridine-2-carboxylate is a heterocyclic organic compound characterized by its complex structure, which includes a thieno[2,3-b]pyridine ring system. This compound features an ethyl ester functional group, an amino group, and a bromine substituent, contributing to its unique chemical properties. The presence of the bromine atom typically enhances the compound's reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The amino group can participate in hydrogen bonding and may influence the compound's solubility and biological activity. Ethyl 3-amino-5-bromothieno[2,3-b]pyridine-2-carboxylate may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in targeting specific biological pathways. As with many heterocycles, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in both laboratory and industrial settings.

Formula: C₁₀H₉BrN₂O₂S

InChI: InChI=1S/C10H9BrN2O2S/c1-2-15-10(14)8-7(12)6-3-5(11)4-13-9(6)16-8/h3-4H,2,12H2,1H3

InChI key: InChIKey=OFFUKMQZOCHIJU-UHFFFAOYSA-N

SMILES: NC=1C=2C(SC1C(OCC)=O)=NC=C(Br)C2

Synonyms:

• Thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-5-bromo-, ethyl ester
• Ethyl 3-amino-5-bromothieno[2,3-b]pyridine-2-carboxylate

ethyl3-amino-5-bromothieno[2,3-b]pyridine-2-carboxylate

CAS: 1234616-31-9

Formula: C₁₀H₉BrN₂O₂S

Purity: 97%

Color and Shape: Solid

Molecular weight: 301.1597

Ref: IN-DA00HHAG

ETHYL 3-AMINO-5-BROMOTHIENO[2,3-B]PYRIDINE-2-CARBOXYLATE

CAS: 1234616-31-9

Formula: C₁₀H₉BrN₂O₂S

Purity: 97%

Molecular weight: 301.16

Ref: 10-F502526