CAS 3197-44-2
:(2S)-piperidin-2-ylmethanol
Description:
(2S)-piperidin-2-ylmethanol, with the CAS number 3197-44-2, is an organic compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The "2S" designation indicates that the compound has a specific stereochemistry at the second carbon atom, which is crucial for its biological activity and interactions. This compound features a hydroxymethyl group (-CH2OH) attached to the nitrogen-containing ring, contributing to its properties as an alcohol. It is typically a colorless to pale yellow liquid or solid, depending on the conditions, and is soluble in water and various organic solvents. The presence of the hydroxyl group makes it a potential candidate for various chemical reactions, including esterification and etherification. Additionally, (2S)-piperidin-2-ylmethanol may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its structural features allow for interactions with biological targets, which can be explored in pharmacological studies.
Formula:C6H13NO
InChI:InChI=1/C6H13NO/c8-5-6-3-1-2-4-7-6/h6-8H,1-5H2/t6-/m0/s1
SMILES:C1CCN[C@@H](C1)CO
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Found 4 products.
(2R)-piperidin-2-ylmethanol
CAS:Formula:C6H13NOPurity:95%Color and Shape:SolidMolecular weight:115.1735(2R)-piperidin-2-ylmethanol
CAS:<p>(2R)-piperidin-2-ylmethanol</p>Purity:95%Molecular weight:115.17g/mol(R)-Piperidin-2-ylmethanol
CAS:Formula:C6H13NOPurity:95%Color and Shape:LiquidMolecular weight:115.176(2R)-piperidin-2-ylmethanol
CAS:<p>(2R)-Piperidin-2-ylmethanol is a chiral, enantioselective olefin with an aziridine ring. The synthesis of this compound is by a Wittig reaction, which is a type of olefination. This reaction involves the use of an organometallic reagent and a phosphonium salt to form a new carbon-carbon bond between two unactivated alkenes.<br>INTERNATIONAL CLASSIFICATION</p>Formula:C6H13NOPurity:Min. 95%Molecular weight:115.17 g/mol



