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Atomfair Benzyl tert-butyl ethane-1,2-diyldicarbamate N-CBZ-N’-BOC-ETHYLENEDIAMINE, 1-CBZ-AMINO-2-BOC-AMINO-ETHANE C15H22N2O4

Description Benzyl tert-butyl ethane-1,2-diyldicarbamate (CAS No. 77153-05-0) is a high-purity organic compound with the molecular formula C15H22N2O4. Also known by its IUPAC name benzyl N-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethyl]carbamate , this specialized chemical is widely utilized in peptide synthesis and pharmaceutical research as a protecting group reagent. The compound features both benzyloxycarbonyl (Cbz) and tert-butoxycarbonyl (Boc) protecting groups, making it invaluable for orthogonal protection strategies in complex organic syntheses. Our product is rigorously tested to ensure ??95% purity (HPLC) and is supplied as a white to off-white crystalline powder, packaged under inert conditions to guarantee stability. Ideal for researchers requiring precise control over amine…

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Description

Description

Benzyl tert-butyl ethane-1,2-diyldicarbamate (CAS No. 77153-05-0) is a high-purity organic compound with the molecular formula C15H22N2O4. Also known by its IUPAC name benzyl N-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethyl]carbamate, this specialized chemical is widely utilized in peptide synthesis and pharmaceutical research as a protecting group reagent. The compound features both benzyloxycarbonyl (Cbz) and tert-butoxycarbonyl (Boc) protecting groups, making it invaluable for orthogonal protection strategies in complex organic syntheses. Our product is rigorously tested to ensure ??95% purity (HPLC) and is supplied as a white to off-white crystalline powder, packaged under inert conditions to guarantee stability. Ideal for researchers requiring precise control over amine protection/deprotection steps in multi-step synthetic routes.

  • CAS No: 77153-05-0
  • Molecular Formula: C15H22N2O4
  • Molecular Weight: 294.35
  • Exact Mass: 294.15795719
  • Monoisotopic Mass: 294.15795719
  • IUPAC Name: benzyl N-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethyl]carbamate
  • SMILES: CC(C)(C)OC(=O)NCCNC(=O)OCC1=CC=CC=C1
  • Synonyms: 77153-05-0, Benzyl tert-butyl ethane-1,2-diyldicarbamate, N-CBZ-N’-BOC-ETHYLENEDIAMINE, 1-CBZ-AMINO-2-BOC-AMINO-ETHANE, NSC668025

Application

Benzyl tert-butyl ethane-1,2-diyldicarbamate serves as a dual-protected diamine building block in solid-phase peptide synthesis (SPPS), enabling selective deprotection of either the Cbz or Boc groups under different conditions. The compound finds particular utility in medicinal chemistry for constructing complex molecular architectures requiring differentiated amine protection. Its orthogonal protecting group combination allows sequential deprotection strategies essential for synthesizing branched peptides and heterocyclic compounds. Researchers also employ this reagent in the development of novel drug candidates where controlled amine reactivity is required.

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