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Atomfair Formamide, N-(2-hydroxy-1,1-dimethylethyl)- C5H11NO2

Description Formamide, N-(2-hydroxy-1,1-dimethylethyl)- (CAS: 104863-65-2) is a high-purity organic compound with the molecular formula C5H11NO2. Also known as N-(1-hydroxy-2-methylpropan-2-yl)formamide , this specialized chemical is designed for research and industrial applications requiring precise reactivity and solubility. Its unique structure, featuring both hydroxyl and formamide functional groups, makes it a versatile intermediate in organic synthesis, pharmaceutical development, and material science. Suitable for laboratory use, this product is rigorously tested for purity and stability, ensuring reliable performance in sensitive reactions. Available in various quantities to meet your research needs.

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Description

Description

Formamide, N-(2-hydroxy-1,1-dimethylethyl)- (CAS: 104863-65-2) is a high-purity organic compound with the molecular formula C5H11NO2. Also known as N-(1-hydroxy-2-methylpropan-2-yl)formamide, this specialized chemical is designed for research and industrial applications requiring precise reactivity and solubility. Its unique structure, featuring both hydroxyl and formamide functional groups, makes it a versatile intermediate in organic synthesis, pharmaceutical development, and material science. Suitable for laboratory use, this product is rigorously tested for purity and stability, ensuring reliable performance in sensitive reactions. Available in various quantities to meet your research needs.

  • CAS No: 104863-65-2
  • Molecular Formula: C5H11NO2
  • Molecular Weight: 117.15
  • Exact Mass: 117.078978594
  • Monoisotopic Mass: 117.078978594
  • IUPAC Name: N-(1-hydroxy-2-methylpropan-2-yl)formamide
  • SMILES: CC(C)(CO)NC=O
  • Synonyms: 682-85-9, Formamide, N-(2-hydroxy-1,1-dimethylethyl)-, DTXSID40330257, DTXCID00281352, N-(1-hydroxy-2-methylpropan-2-yl)formamide

Application

Formamide, N-(2-hydroxy-1,1-dimethylethyl)- is widely used as a key intermediate in the synthesis of pharmaceuticals and fine chemicals. Its hydroxyl and amide functionalities enable participation in condensation, esterification, and nucleophilic substitution reactions. Researchers utilize this compound in the development of bioactive molecules and polymer precursors. It is also employed in specialty solvent formulations due to its balanced polarity and solubility properties.

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