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Atomfair tert-Butyl indoline-1-carboxylate C13H17NO2

Description tert-Butyl indoline-1-carboxylate (CAS No. 143262-10-6) is a high-purity organic compound with the molecular formula C13H17NO2. This derivative of indoline features a tert-butyl carbamate group, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. Its IUPAC name, tert-butyl 2,3-dihydroindole-1-carboxylate , reflects its structural precision. The compound is supplied as a crystalline solid with ??95% purity (HPLC), ensuring consistency for research and industrial applications. Ideal for use in N-protection strategies, cross-coupling reactions, and heterocyclic chemistry, it is packaged under inert gas to maintain stability. Available in quantities from grams to kilograms, with custom synthesis options upon request.

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Description

Description

tert-Butyl indoline-1-carboxylate (CAS No. 143262-10-6) is a high-purity organic compound with the molecular formula C13H17NO2. This derivative of indoline features a tert-butyl carbamate group, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. Its IUPAC name, tert-butyl 2,3-dihydroindole-1-carboxylate, reflects its structural precision. The compound is supplied as a crystalline solid with ??95% purity (HPLC), ensuring consistency for research and industrial applications. Ideal for use in N-protection strategies, cross-coupling reactions, and heterocyclic chemistry, it is packaged under inert gas to maintain stability. Available in quantities from grams to kilograms, with custom synthesis options upon request.

  • CAS No: 143262-10-6
  • Molecular Formula: C13H17NO2
  • Molecular Weight: 219.28
  • Exact Mass: 219.125928785
  • Monoisotopic Mass: 219.125928785
  • IUPAC Name: tert-butyl 2,3-dihydroindole-1-carboxylate
  • SMILES: CC(C)(C)OC(=O)N1CCC2=CC=CC=C21
  • Synonyms: 143262-10-6, tert-Butyl indoline-1-carboxylate, DTXSID30394808, DTXCID80345668, 623-971-8

Application

tert-Butyl indoline-1-carboxylate serves as a key building block in medicinal chemistry for the synthesis of indoline-based drug candidates. It is widely used as a protective group for nitrogen in peptide and heterocycle synthesis. The compound also finds applications in catalytic asymmetric hydrogenation studies and as a precursor for functionalized indoles. Researchers leverage its stability in multi-step organic transformations to develop novel bioactive molecules.

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