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Atomfair tert-butyl N-(2-hydroxycyclopentyl)carbamate C10H19NO3

Description tert-butyl N-(2-hydroxycyclopentyl)carbamate (CAS No. 454170-16-2) is a high-purity carbamate derivative with the molecular formula C10H19NO3. This compound features a cyclopentyl backbone substituted with a hydroxyl group and a tert-butoxycarbonyl (Boc) protected amine, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its well-defined structure ensures consistent reactivity, ideal for peptide coupling, medicinal chemistry, and scaffold diversification. Available in >95% purity (HPLC/GC), this product is rigorously tested for quality, including NMR and mass spectrometry verification. Packaged under inert conditions to ensure stability, it is suited for laboratory and industrial-scale applications.

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Description

Description

tert-butyl N-(2-hydroxycyclopentyl)carbamate (CAS No. 454170-16-2) is a high-purity carbamate derivative with the molecular formula C10H19NO3. This compound features a cyclopentyl backbone substituted with a hydroxyl group and a tert-butoxycarbonyl (Boc) protected amine, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its well-defined structure ensures consistent reactivity, ideal for peptide coupling, medicinal chemistry, and scaffold diversification. Available in >95% purity (HPLC/GC), this product is rigorously tested for quality, including NMR and mass spectrometry verification. Packaged under inert conditions to ensure stability, it is suited for laboratory and industrial-scale applications.

  • CAS No: 454170-16-2
  • Molecular Formula: C10H19NO3
  • Molecular Weight: 201.26
  • Exact Mass: 201.13649347
  • Monoisotopic Mass: 201.13649347
  • IUPAC Name: tert-butyl N-(2-hydroxycyclopentyl)carbamate
  • SMILES: CC(C)(C)OC(=O)NC1CCCC1O
  • Synonyms: tert-butyl N-(2-hydroxycyclopentyl)carbamate, DTXSID70333251, DTXCID80284341, 945652-35-7, tert-butyl (2-hydroxycyclopentyl)carbamate

Application

tert-butyl N-(2-hydroxycyclopentyl)carbamate is widely used as a protected amine intermediate in the synthesis of bioactive molecules and peptidomimetics. Its Boc group enables selective deprotection under mild acidic conditions, facilitating stepwise organic transformations. Researchers leverage this compound in drug discovery for constructing chiral cyclopentane-based scaffolds. It also serves as a precursor for catalysts and ligands in asymmetric synthesis.

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