CAS 218780-53-1

1-N-(Methylsulfonyl)-4-piperidinone

Description:

1-N-(Methylsulfonyl)-4-piperidinone, identified by its CAS number 218780-53-1, is a chemical compound characterized by its piperidinone structure, which features a piperidine ring with a ketone functional group and a methylsulfonyl substituent. This compound typically exhibits properties associated with both amines and sulfonyl groups, making it polar and potentially soluble in polar solvents such as water and alcohols. The presence of the methylsulfonyl group may impart unique reactivity, influencing its behavior in chemical reactions and interactions with biological systems. It is often studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. Additionally, the compound may exhibit specific pharmacological properties, although detailed studies would be necessary to elucidate its full biological profile. Safety data and handling precautions should be considered, as with any chemical substance, to ensure proper laboratory practices.

Formula: C₆H₁₁NO₃S

InChI: InChI=1/C6H11NO3S/c1-11(9,10)7-4-2-6(8)3-5-7/h2-5H2,1H3

SMILES: CS(=O)(=O)N1CCC(=O)CC1

Synonyms:

• 4-Piperidinone, 1-(Methylsulfonyl)-
• 1-(Methylsulfonyl)Piperidin-4-One
• 1-(Methylsulfonyl)-4-piperidinone

1-N-(METHYLSULFONYL)-4-PIPERIDINONE

CAS: 218780-53-1

Formula: C₆H₁₁NO₃S

Purity: 98%

Color and Shape: Solid

Molecular weight: 177.2214

Ref: IN-DA006YZ7

1-(Methylsulphonyl)piperidin-4-one

CAS: 218780-53-1

1-(Methylsulphonyl)piperidin-4-one

Formula: C₆H₁₁NO₃S

Purity: ≥95%

Color and Shape: colourless crystals

Molecular weight: 177.22g/mol

Ref: 54-OR16033

1-(Methylsulfonyl)-4-piperidinone

CAS: 218780-53-1

M04157 - 1-(Methylsulfonyl)-4-piperidinone

Formula: C₆H₁₁NO₃S

Purity: 98%

Color and Shape: Solid

Molecular weight: 177.22

Ref: 10-M04157

1-N-(methylsulfonyl)-4-piperidinone

CAS: 218780-53-1

1-N-(methylsulfonyl)-4-piperidinone is a compound that belongs to the group of secondary organic amines. It can be used as an intermediate in the synthesis of p-hydroxybenzoic acid and hydroxyl group compounds. 1-N-(methylsulfonyl)-4-piperidinone has been shown to inhibit protein synthesis in cultured cells by blocking the formation of aminoacyl-tRNA and preventing translocation of peptide chain from ribosomes to the site of peptide bond formation. This process is essential for the production of proteins, which are necessary for normal cell function. The inhibitory effect on protein synthesis was also observed when 1-N-(methylsulfonyl)-4-piperidinone was incubated with human erythrocytes, an enzyme isolated from calf thymus, and a monoclonal antibody (mAb). This mechanism is believed to be due

Formula: C₆H₁₁NO₃S

Purity: Min. 95%

Molecular weight: 177.22 g/mol

Ref: 3D-TIA78053