5000-48-6 Usage
Description
4-CHLOROPHENYLSULFONYLACETONE, also known as (4-Chlorophenylsulfonyl)acetone, is an antiviral sulfonyl compound characterized by its off-white crystalline powder appearance. It is a synthetic chemical with potential applications in various industries due to its unique properties.
Uses
Used in Pharmaceutical Industry:
4-CHLOROPHENYLSULFONYLACETONE is used as an antiviral agent for its ability to inhibit viral replication and activity. It is particularly effective against a range of viruses, making it a valuable compound in the development of antiviral medications and treatments.
Used in Chemical Research:
In the field of chemical research, 4-CHLOROPHENYLSULFONYLACETONE serves as an important intermediate compound in the synthesis of various pharmaceuticals and other specialty chemicals. Its unique structure allows for further modification and functionalization, leading to the creation of new molecules with specific applications.
Used in Material Science:
4-CHLOROPHENYLSULFONYLACETONE can be utilized in the development of novel materials with enhanced properties, such as improved stability, durability, or biocompatibility. Its integration into material formulations can lead to the creation of advanced materials for various applications, including medical devices, coatings, and adhesives.
Used in Agrochemical Industry:
In the agrochemical industry, 4-CHLOROPHENYLSULFONYLACETONE may be employed as a component in the development of new pesticides or herbicides. Its antiviral properties could potentially be harnessed to control the spread of plant viruses, thereby improving crop yields and protecting agricultural resources.
Overall, 4-CHLOROPHENYLSULFONYLACETONE is a versatile compound with a wide range of applications across different industries, primarily due to its antiviral properties and its potential use as a key intermediate in the synthesis of various chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 5000-48-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5000-48:
(6*5)+(5*0)+(4*0)+(3*0)+(2*4)+(1*8)=46
46 % 10 = 6
So 5000-48-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClO3S/c1-7(11)6-14(12,13)9-4-2-8(10)3-5-9/h2-5H,6H2,1H3
5000-48-6Relevant articles and documents
Facile One-Pot Access to α-Diazo-β-ketosulfones from Sulfonyl Chlorides and α-Haloketones
Dar'In, Dmitry,Kantin, Grigory,Bakulina, Olga,Krasavin, Mikhail
, p. 2259 - 2266 (2020/08/26)
A convenient one-pot approach to the preparation of α-diazo-β-ketosulfones from sulfonyl chlorides is described. It involves the conversion of the sulfonyl chloride to sodium sulfinate, alkylation of the latter with α-haloketones followed by diazo transfer using the 'sulfonyl-azide-free' ('SAFE') protocol in aqueous medium. The simple and expedient method relies on readily available starting materials and provides facile access to a wide variety of valuable diazo reagents for organic synthesis.
(Arylsulfonyl)acetones and -acetonitriles: New activated methylenic building blocks for synthesis of 1,2,3-triazoles
Pokhodylo, Nazariy T.,Matiychuk, Vasyl S.,Obushak, Mykola D.
scheme or table, p. 2321 - 2323 (2010/02/16)
β-Keto sulfones and b-nitrile sulfones were used as building blocks for 1,2,3-triazole synthesis in the Dimroth cyclization. It was shown, that sulfone reagents undergo base-catalyzed cyclization under mild conditions (at room temperature) to give 1,2,3-triazoles in moderate to excellent yields. This fact has confirmed the high nucleophilicity of sulfonylmethylenic compounds and allows new synthetic applications. Georg Thieme Verlag Stuttgart.
RAPID AMD LARGE-SCALE SYNTHESIS OF SULFONYL-SUBSTITUTED PROPANONES
Davis, Roman
, p. 823 - 828 (2007/10/02)
A one-pot, large-scale, and rapid (10-20 minutes) synthesis of sulfonyl-substituted propanone has been developed.The synthesis, starting with a thiol, chloroacetone, and OXONE, can easily be monitored with the use of a pH indicator.
