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Atomfair ethyl 4H-furo[3,2-b]pyrrole-5-carboxylate C9H9NO3
Description Ethyl 4H-furo[3,2-b]pyrrole-5-carboxylate (CAS No. 35405-94-8) is a high-purity heterocyclic organic compound with the molecular formula C9H9NO3. This specialized chemical features a fused furopyrrole core, making it a valuable intermediate in pharmaceutical and agrochemical research. With a molecular weight of 179.17 g/mol, this ester derivative exhibits excellent reactivity for further functionalization. Our product is rigorously tested to ensure ??95% purity by HPLC, with detailed analytical data (GC/MS, NMR) available upon request. Supplied in amber glass vials under inert atmosphere to ensure stability, this compound is ideal for medicinal chemistry, material science, and synthetic methodology development.
Description
Description
Ethyl 4H-furo[3,2-b]pyrrole-5-carboxylate (CAS No. 35405-94-8) is a high-purity heterocyclic organic compound with the molecular formula C9H9NO3. This specialized chemical features a fused furopyrrole core, making it a valuable intermediate in pharmaceutical and agrochemical research. With a molecular weight of 179.17 g/mol, this ester derivative exhibits excellent reactivity for further functionalization. Our product is rigorously tested to ensure ??95% purity by HPLC, with detailed analytical data (GC/MS, NMR) available upon request. Supplied in amber glass vials under inert atmosphere to ensure stability, this compound is ideal for medicinal chemistry, material science, and synthetic methodology development.
- CAS No: 35405-94-8
- Molecular Formula: C9H9NO3
- Molecular Weight: 179.17
- Exact Mass: 179.058243149
- Monoisotopic Mass: 179.058243149
- IUPAC Name: ethyl 4H-furo[3,2-b]pyrrole-5-carboxylate
- SMILES: CCOC(=O)C1=CC2=C(N1)C=CO2
- Synonyms: ethyl 4H-furo[3,2-b]pyrrole-5-carboxylate, 35405-94-8, Ethyl furo[3,2-b]pyrrole-5-carboxylate, 4h-furo[3,2-b]pyrrole-5-carboxylic acid ethyl ester, NNABKJKQNGGLKM-UHFFFAOYSA
Application
This compound serves as a key building block in the synthesis of novel heterocyclic pharmaceuticals, particularly for CNS-targeting agents. Researchers utilize it in palladium-catalyzed cross-coupling reactions to create complex molecular architectures. The furopyrrole scaffold shows promise in developing new antimicrobial and anti-inflammatory compounds. Its ester functionality allows for straightforward derivatization to amides or carboxylic acids.
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