Atomfair 5-Bromothiophene-3-carboxamide C5H4BrNOS

Description 5-Bromothiophene-3-carboxamide (CAS No. 189329-94-0) is a high-purity brominated thiophene derivative with the molecular formula C5H4BrNOS . This compound is a valuable intermediate in organic synthesis and pharmaceutical research, featuring a reactive bromine substituent and a carboxamide functional group for further derivatization. Its thiophene backbone contributes to unique electronic properties, making it useful in materials science and medicinal chemistry applications. Our product is rigorously tested for purity and consistency, ensuring optimal performance in your research workflows. Available in various quantities, this compound is ideal for researchers seeking reliable building blocks for heterocyclic chemistry, drug discovery, and agrochemical development.

Description

5-Bromothiophene-3-carboxamide (CAS No. 189329-94-0) is a high-purity brominated thiophene derivative with the molecular formula C₅H₄BrNOS. This compound is a valuable intermediate in organic synthesis and pharmaceutical research, featuring a reactive bromine substituent and a carboxamide functional group for further derivatization. Its thiophene backbone contributes to unique electronic properties, making it useful in materials science and medicinal chemistry applications. Our product is rigorously tested for purity and consistency, ensuring optimal performance in your research workflows. Available in various quantities, this compound is ideal for researchers seeking reliable building blocks for heterocyclic chemistry, drug discovery, and agrochemical development.

CAS No: 189329-94-0
Molecular Formula: C5H4BrNOS
Molecular Weight: 206.06
Exact Mass: 204.91970
Monoisotopic Mass: 204.91970
IUPAC Name: 5-bromothiophene-3-carboxamide
SMILES: C1=C(SC=C1C(=O)N)Br
Synonyms: 5-bromothiophene-3-carboxamide, 189329-94-0, DTXSID90596664, DTXCID60547426, 865-058-9

Application

5-Bromothiophene-3-carboxamide serves as a versatile scaffold in medicinal chemistry for the synthesis of bioactive molecules targeting various diseases. Its bromine moiety enables cross-coupling reactions (e.g., Suzuki, Heck) for constructing complex thiophene-based architectures. Researchers utilize this compound in developing potential kinase inhibitors, antimicrobial agents, and functional materials due to its electron-rich heterocyclic core. The carboxamide group facilitates hydrogen bonding interactions in drug-receptor binding studies.

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