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Atomfair methyl 5-(hydroxymethyl)-1H-pyrrole-2-carboxylate C7H9NO3

Description Methyl 5-(hydroxymethyl)-1H-pyrrole-2-carboxylate (CAS No. 1215961-78-6) is a high-purity heterocyclic compound with the molecular formula C7H9NO3. This specialized chemical features a pyrrole ring substituted with both a hydroxymethyl group at the 5-position and a methyl ester at the 2-position, offering versatile reactivity for synthetic applications. With a molecular weight of 155.15 g/mol, this compound is ideal for researchers in medicinal chemistry, organic synthesis, and material science. Available in >95% purity (HPLC), it is supplied in sealed packaging under inert conditions to ensure stability. Suitable for use as a building block in pharmaceutical intermediates, ligand design, and polymer chemistry. Store at…

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Description

Description

Methyl 5-(hydroxymethyl)-1H-pyrrole-2-carboxylate (CAS No. 1215961-78-6) is a high-purity heterocyclic compound with the molecular formula C7H9NO3. This specialized chemical features a pyrrole ring substituted with both a hydroxymethyl group at the 5-position and a methyl ester at the 2-position, offering versatile reactivity for synthetic applications. With a molecular weight of 155.15 g/mol, this compound is ideal for researchers in medicinal chemistry, organic synthesis, and material science. Available in >95% purity (HPLC), it is supplied in sealed packaging under inert conditions to ensure stability. Suitable for use as a building block in pharmaceutical intermediates, ligand design, and polymer chemistry. Store at 2-8??C in a dry environment.

  • CAS No: 1215961-78-6
  • Molecular Formula: C7H9NO3
  • Molecular Weight: 155.15
  • Exact Mass: 155.058243149
  • Monoisotopic Mass: 155.058243149
  • IUPAC Name: methyl 5-(hydroxymethyl)-1H-pyrrole-2-carboxylate
  • SMILES: COC(=O)C1=CC=C(N1)CO
  • Synonyms: Methyl 5-(hydroxymethyl)-1H-pyrrole-2-carboxylate, 1215961-78-6, 991-458-9, QYB96178, MFCD12402320

Application

Methyl 5-(hydroxymethyl)-1H-pyrrole-2-carboxylate serves as a key intermediate in the synthesis of bioactive pyrrole derivatives for drug discovery. Its bifunctional reactivity enables conjugation with peptides or nucleosides in pharmaceutical research. The compound is also employed in catalytic studies and as a precursor for functionalized polymers with optoelectronic properties.

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