Bromoterthiophenecarboxaldehyde, identified by its CAS number 161726-69-8, is an organic compound that features a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of a bromine atom and a carboxaldehyde functional group contributes to its reactivity and potential applications in organic synthesis. This compound is characterized by its distinctive odor, typical of aldehydes, and its ability to participate in various chemical reactions, such as nucleophilic additions and electrophilic substitutions. The bromine substituent can enhance the electrophilicity of the carbonyl carbon, making it a useful intermediate in the synthesis of more complex molecules. Additionally, the thiophene moiety can impart unique electronic properties, making this compound of interest in materials science and medicinal chemistry. Its solubility in organic solvents and stability under standard laboratory conditions further facilitate its use in research and industrial applications. As with many brominated compounds, caution should be exercised due to potential toxicity and environmental impact.

Bromoterthiophenecarboxaldehyde

161726-69-8: 5-Bromo-2,2:5,2-terthiophene-5-carboxaldehyde

5''-Bromo-2,2':5',2''-terthiophene-5-carboxaldehyde

[2,2':5',2''-Terthiophene]-5-carboxaldehyde, 5''-bromo-

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CAS 161726-69-8: Bromoterthiophenecarboxaldehyde

5''-Bromo-2,2':5',2''-terthiophene-5-carboxaldehyde

Ref: 54-OR310297

[2,2':5',2''-Terthiophene]-5-carboxaldehyde, 5''-bromo-

Ref: IN-DA001VUO

5''-Bromo-2,2:5',2''-terthiophene-5-carboxaldehyde

Ref: 3D-FB41102

5''-Bromo-2,2':5',2''-terthiophene-5-carboxaldehyde

Ref: 3B-B2058

5''-Bromo-2,2'-5',2''-terthiophene-5-carboxaldehyde

Ref: 10-F050869