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Atomfair tert-butyl 3-formyl-1H-indole-1-carboxylate C14H15NO3
Description tert-Butyl 3-formyl-1H-indole-1-carboxylate (CAS No. 57476-50-3) is a high-purity, synthetic organic compound with the molecular formula C14H15NO3. This indole derivative features a formyl group at the 3-position and a Boc (tert-butoxycarbonyl) protecting group at the 1-position, making it a versatile intermediate in pharmaceutical and agrochemical synthesis. Its IUPAC name is tert-butyl 3-formylindole-1-carboxylate , and it is characterized by excellent stability under standard storage conditions. This compound is supplied as a crystalline solid with ??95% purity (HPLC), ensuring reliable performance in demanding research applications. Ideal for use in medicinal chemistry, it serves as a key precursor for the development of indole-based…
Description
Description
tert-Butyl 3-formyl-1H-indole-1-carboxylate (CAS No. 57476-50-3) is a high-purity, synthetic organic compound with the molecular formula C14H15NO3. This indole derivative features a formyl group at the 3-position and a Boc (tert-butoxycarbonyl) protecting group at the 1-position, making it a versatile intermediate in pharmaceutical and agrochemical synthesis. Its IUPAC name is tert-butyl 3-formylindole-1-carboxylate, and it is characterized by excellent stability under standard storage conditions. This compound is supplied as a crystalline solid with ??95% purity (HPLC), ensuring reliable performance in demanding research applications. Ideal for use in medicinal chemistry, it serves as a key precursor for the development of indole-based bioactive molecules, including kinase inhibitors and serotonin receptor modulators.
- CAS No: 57476-50-3
- Molecular Formula: C14H15NO3
- Molecular Weight: 245.27
- Exact Mass: 245.10519334
- Monoisotopic Mass: 245.10519334
- IUPAC Name: tert-butyl 3-formylindole-1-carboxylate
- SMILES: CC(C)(C)OC(=O)N1C=C(C2=CC=CC=C21)C=O
- Synonyms: 57476-50-3, tert-butyl 3-formyl-1H-indole-1-carboxylate, DTXSID10377477, DTXCID10328505, 827-428-8
Application
tert-Butyl 3-formyl-1H-indole-1-carboxylate is widely used as a building block in the synthesis of indole-containing pharmaceuticals, particularly in the development of kinase inhibitors and CNS-active compounds. Its reactive formyl group enables facile derivatization via condensation or nucleophilic addition reactions. The Boc protecting group enhances solubility and allows selective deprotection under mild acidic conditions, making it valuable for multi-step synthetic routes. Researchers employ this compound in the construction of complex heterocycles for drug discovery programs.
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