CAS 141482-19-1

4-Piperidinol, 1-(methylsulfonyl)-

Description:

4-Piperidinol, 1-(methylsulfonyl)- is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The presence of a hydroxyl group (-OH) at the 4-position of the piperidine ring contributes to its classification as a piperidinol. Additionally, the methylsulfonyl group (-SO2CH3) at the 1-position enhances its solubility in polar solvents and may influence its reactivity and biological activity. This compound is typically a white to off-white solid and is soluble in water and organic solvents. It may exhibit properties such as being a potential intermediate in organic synthesis or having pharmacological applications, although specific biological activities would depend on further research. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken. Overall, 4-Piperidinol, 1-(methylsulfonyl)- is of interest in both synthetic chemistry and potential medicinal applications.

Formula: C₆H₁₃NO₃S

4-Piperidinol, 1-(methylsulfonyl)-

CAS: 141482-19-1

Formula: C₆H₁₃NO₃S

Purity: 97%

Color and Shape: Solid

Molecular weight: 179.2373

Ref: IN-DA001GGX

4-Hydroxy-1-(methylsulphonyl)piperidine

CAS: 141482-19-1

4-Hydroxy-1-(methylsulphonyl)piperidine

Purity: 95%

Color and Shape: Solid

Molecular weight: 179.24g/mol

Ref: 54-OR200068

1-(Methylsulfonyl)piperidin-4-ol

CAS: 141482-19-1

Formula: C₆H₁₃NO₃S

Purity: 97%

Color and Shape: Solid

Molecular weight: 179.23

Ref: 10-F232060

4-Hydroxy-1-(methylsulphonyl)piperidine

CAS: 141482-19-1

4-Hydroxy-1-(methylsulphonyl)piperidine is a novel linker molecule that has been designed to be orally bioavailable. It is hydrophobic and has been optimized for interaction with protein-coupled receptors. This linker molecule has shown excellent plasma glucose lowering effects in animal studies, which may be due to its ability to reduce insulin resistance and increase insulin sensitivity. The conformational and conformationally dependent interactions of this compound with the receptor are expected to improve oral bioavailability. 4-Hydroxy-1-(methylsulphonyl)piperidine also inhibits the activity of protein kinase C (PKC), although it does not inhibit phosphodiesterase or adenylate cyclase activities.

Formula: C₆H₁₃NO₃S

Purity: Min. 95%

Molecular weight: 179.24 g/mol

Ref: 3D-RFA48219