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Atomfair Prolinol C5H11NO
Description Prolinol (Pyrrolidin-2-ylmethanol) is a versatile chiral building block and intermediate widely utilized in organic synthesis and pharmaceutical research. With the molecular formula C5H11NO and CAS number 107504-08-5 , this compound features a pyrrolidine ring with a hydroxymethyl substituent, offering unique reactivity for asymmetric synthesis and ligand design. Prolinol is available in high purity (>98%) and is supplied as a clear, colorless to pale yellow liquid under standard conditions. Its structural properties make it valuable for the preparation of chiral catalysts, peptidomimetics, and bioactive molecules. Proper storage in a cool, dry place under inert atmosphere is recommended to ensure stability.
Description
Description
Prolinol (Pyrrolidin-2-ylmethanol) is a versatile chiral building block and intermediate widely utilized in organic synthesis and pharmaceutical research. With the molecular formula C5H11NO and CAS number 107504-08-5, this compound features a pyrrolidine ring with a hydroxymethyl substituent, offering unique reactivity for asymmetric synthesis and ligand design. Prolinol is available in high purity (>98%) and is supplied as a clear, colorless to pale yellow liquid under standard conditions. Its structural properties make it valuable for the preparation of chiral catalysts, peptidomimetics, and bioactive molecules. Proper storage in a cool, dry place under inert atmosphere is recommended to ensure stability.
- CAS No: 107504-08-5
- Molecular Formula: C5H11NO
- Molecular Weight: 101.15
- Exact Mass: 101.084063974
- Monoisotopic Mass: 101.084063974
- IUPAC Name: pyrrolidin-2-ylmethanol
- SMILES: C1CC(NC1)CO
- Synonyms: pyrrolidin-2-ylmethanol, 498-63-5, Prolinol, (pyrrolidin-2-yl)methanol, pyrrolidine-2-methanol
Application
Prolinol is extensively employed as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantioselective catalysts and ligands. It serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Researchers also utilize Prolinol for the development of peptidomimetics and proline-based organocatalysts due to its stereochemical flexibility.
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