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Atomfair 3-(Aminomethyl)-3-(hydroxymethyl)cyclobutan-1-one C6H11NO2

Description 3-(Aminomethyl)-3-(hydroxymethyl)cyclobutan-1-one (CAS No. 1340170-98-0) is a high-purity cyclobutanone derivative with the molecular formula C6H11NO2. This specialized organic compound features both aminomethyl and hydroxymethyl functional groups, making it a versatile intermediate for synthetic organic chemistry and pharmaceutical research. With an IUPAC name of 3-(aminomethyl)-3-(hydroxymethyl)cyclobutan-1-one, this compound is supplied as a white to off-white crystalline powder with ??95% purity (HPLC). It is ideal for use in medicinal chemistry, peptide synthesis, and the development of novel heterocyclic compounds. Store in a cool, dry place under inert conditions to ensure stability.

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Description

Description

3-(Aminomethyl)-3-(hydroxymethyl)cyclobutan-1-one (CAS No. 1340170-98-0) is a high-purity cyclobutanone derivative with the molecular formula C6H11NO2. This specialized organic compound features both aminomethyl and hydroxymethyl functional groups, making it a versatile intermediate for synthetic organic chemistry and pharmaceutical research. With an IUPAC name of 3-(aminomethyl)-3-(hydroxymethyl)cyclobutan-1-one, this compound is supplied as a white to off-white crystalline powder with ??95% purity (HPLC). It is ideal for use in medicinal chemistry, peptide synthesis, and the development of novel heterocyclic compounds. Store in a cool, dry place under inert conditions to ensure stability.

  • CAS No: 1340170-98-0
  • Molecular Formula: C6H11NO2
  • Molecular Weight: 129.16
  • Exact Mass: 129.078978594
  • Monoisotopic Mass: 129.078978594
  • IUPAC Name: 3-(aminomethyl)-3-(hydroxymethyl)cyclobutan-1-one
  • SMILES: C1C(=O)CC1(CN)CO
  • Synonyms: 3-(aminomethyl)-3-(hydroxymethyl)cyclobutan-1-one, 1340170-98-0, AKOS014234441, EN300-1250337

Application

This compound serves as a key building block in the synthesis of complex pharmaceutical intermediates, particularly in the development of cyclobutane-based drug candidates. Researchers utilize it in peptide coupling reactions and as a precursor for functionalized cyclobutanones. Its bifunctional reactivity (amine and alcohol groups) enables diverse modifications for targeted molecular design.

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