CAS 5000-44-2

Phenylsulfonylacetone

Description:

Phenylsulfonylacetone, with the CAS number 5000-44-2, is an organic compound characterized by its sulfonyl functional group attached to a phenyl ring and an acetone moiety. It typically appears as a white to off-white crystalline solid. This compound is known for its role in organic synthesis, particularly in the formation of various derivatives and as a reagent in chemical reactions. It exhibits moderate solubility in organic solvents, which makes it useful in various applications, including pharmaceuticals and agrochemicals. The presence of the sulfonyl group contributes to its reactivity, allowing it to participate in nucleophilic substitution and other chemical transformations. Additionally, phenylsulfonylacetone may exhibit biological activity, although specific pharmacological properties would require further investigation. As with many sulfonyl compounds, it is important to handle it with care, as it may pose health risks if ingested or inhaled. Overall, phenylsulfonylacetone is a versatile compound with significant utility in synthetic organic chemistry.

Formula: C₉H₁₀O₃S

InChI: InChI=1/C9H10O3S/c1-8(10)7-13(11,12)9-5-3-2-4-6-9/h2-6H,7H2,1H3

SMILES: CC(=O)CS(=O)(=O)c1ccccc1

Synonyms:

• 1-(Phenylsulfonyl)acetone
• 2-Propanone, 1-(phenylsulfonyl)-
• Benzenesulphonylacetone
• 1-(Phenylsulfonyl)Propan-2-One

1-(Phenylsulfonyl)propan-2-one

CAS: 5000-44-2

Formula: C₉H₁₀O₃S

Purity: 97%

Color and Shape: Solid

Molecular weight: 198.2389

Ref: IN-DA003O19

Benzenesulphonyl acetone

CAS: 5000-44-2

Benzenesulphonyl acetone

Purity: 97%

Color and Shape: Solid

Molecular weight: 198.24g/mol

Ref: 54-OR0456

Phenylsulfonylacetone

CAS: 5000-44-2

Formula: C₉H₁₀O₃S

Purity: 97%

Color and Shape: Solid

Molecular weight: 198.24

Ref: 10-F005323

Benzenesulphonylacetone

CAS: 5000-44-2

Benzenesulphonylacetone is an organic solvent with antihypertensive activity. It has been shown in vitro to inhibit the protein kinase, b-raf, and to have antioxidant properties. Benzenesulphonylacetone has been shown to be a competitive inhibitor of the alkoxy radical and the active methylene group, both of which are necessary for the production of asymmetric synthesis. The synthesis of benzenesulphonylacetone can be achieved by reacting methyl sulfones with activated chloride under high pressure and temperature. This process also results in the formation of 2-bromo-3-nitrobenzoic acid, which is then reacted with alkylthio groups to produce benzenesulphonylacetone. Its peptidomimetic form was developed through nitro substitution at position 3 on the benzene ring.

Formula: C₉H₁₀O₃S

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 198.24 g/mol

Ref: 3D-FB169216