Description

tert-Butyl 2-oxo-2,3-dihydro-1H-indole-1-carboxylate (CAS No. 214610-10-3) is a high-purity organic compound with the molecular formula C₁₃H₁₅NO₃. This indole derivative is widely utilized in pharmaceutical research, medicinal chemistry, and organic synthesis due to its versatile reactivity and role as a key intermediate. The compound features a tert-butyl carbamate group attached to the nitrogen of a 2-oxoindoline core, making it valuable for protecting-group strategies and further functionalization.

Our product is rigorously tested to ensure ≥95% purity (HPLC/GC), with detailed analytical data (NMR, MS) available upon request. Supplied as a white to off-white crystalline powder, it is packaged under inert conditions to guarantee stability and longevity. Ideal for researchers requiring reliable building blocks for heterocyclic synthesis, this compound is stored at 2-8°C to maintain optimal quality.

Properties

• CAS Number: 214610-10-3
• Complexity: 332
• IUPAC Name: tert-butyl 2-oxoindoline-1-carboxylate
• InChI: InChI=1S/C13H15NO3/c1-13(2,3)17-12(16)14-10-7-5-4-6-9(10)8-11(14)15/h4-7H,8H2,1-3H3
• InChI Key: UZMPOHKOMYCYCZ-UHFFFAOYSA-N
• Exact Mass: 233.10519334
• Molecular Formula: C13H15NO3
• Molecular Weight: 233.26
• SMILES: CC(C)(C)OC(=O)N1C(=O)CC2=CC=CC=C21
• Topological: 46.6
• Monoisotopic Mass: 233.10519334
• Synonyms: 214610-10-3, tert-Butyl 2-oxo-2,3-dihydro-1H-indole-1-carboxylate, DTXSID20453074, DTXCID80403893, TERT-BUTYL 2-OXOINDOLINE-1-CARBOXYLATE, Tert-butyl 2-oxo-3H-indole-1-carboxylate, 1-Boc-2-oxoindoline, MFCD09032873, 2-OXO-2,3-DIHYDRO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER, N-boc-2-oxyindole, tert-Butyl2-oxoindoline-1-carboxylate, SCHEMBL2419240, UZMPOHKOMYCYCZ-UHFFFAOYSA-N, AKOS015964540, SB64127, tert-butyl 2-oxo-1-indolinecarboxylate, AS-63699, SY124153, DB-120075, CS-0038092, 2-oxo-1,3-dihydro-indole-1-carboxylic acid tert-butyl ester

Application

tert-Butyl 2-oxo-2,3-dihydro-1H-indole-1-carboxylate serves as a critical intermediate in the synthesis of biologically active indole derivatives, including kinase inhibitors and CNS-targeting pharmaceuticals. It is employed in peptide coupling reactions and as a protective group for indole nitrogen in multistep syntheses. Researchers also utilize it to develop novel scaffolds for drug discovery programs targeting inflammation and oncology.

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