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24437-48-7

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24437-48-7 Usage

General Description

1-(4-chlorophenyl)-2-(methylsulfonyl)ethanone is a chemical compound with the molecular formula C9H9ClO3S. It is an organic compound that is used in the synthesis of pharmaceuticals and agrochemicals. 1-(4-CHLOROPHENYL)-2-(METHYLSULFONYL)ETHANONE is also known by the name Ibuprofen Impurity K. It is a white to off-white crystalline powder that is insoluble in water but soluble in organic solvents. This chemical is used as an intermediate in the production of various drugs and is also used in research and development in the pharmaceutical industry. It is important to handle this compound with caution and to use it in a controlled environment due to its potential toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 24437-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,3 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24437-48:
(7*2)+(6*4)+(5*4)+(4*3)+(3*7)+(2*4)+(1*8)=107
107 % 10 = 7
So 24437-48-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClO3S/c1-14(12,13)6-9(11)7-2-4-8(10)5-3-7/h2-5H,6H2,1H3

24437-48-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-Chlorophenyl)-2-methylsulfonylethanone

1.2 Other means of identification

Product number -
Other names 2-(methylsulfonyl)-4'-chloroacetophenone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24437-48-7 SDS

24437-48-7Relevant articles and documents

Copper-catalyzed aerobic oxidative cross-coupling reactions of vinylarenes with sulfinate salts: A direct approach to β-ketosulfones

Chen, Yu,Xu, Lei,Wang, Biyu,Jiang, Jingjing,Sun, Yixiang,Li, Longchun

, (2021/01/25)

A copper-catalyzed aerobic oxidative cross-coupling reactions for the synthesis of β-ketosulfones via formation of a C[sbnd]S bond has been demonstrated. Promoted by the crucial copper catalyst, perfect selectivity and good to excellent yields could be achieved. This method, including inexpensive copper catalyst, wide functional group tolerance, and open air conditions, make it very attractive and practical. More importantly, it also provides a versatile tool for the construction of β-ketosulfones from basic starting materials under mild conditions.

Synthesis of β-ketosulfone derivatives as new non-cytotoxic urease inhibitors in vitro

Iqbal Choudhary, M.,Iqbal, Sarosh,Khan, Ajmal,Khan, Khalid Mohammed,Kiran, Shumaila,Nazir, Rashid,Perveen, Shahnaz

, p. 244 - 255 (2020/03/10)

Background: Peptic ulcer and urolithiasis are largely due to infection caused by urease-producing bacteria. Therefore, the discovery of urease inhibitors is an important area of medicinal chemistry research. Objective: The main aim of the work was to identify novel urease inhibitors with no cytotoxicity. Method: During the current study, a series of β-ketosulfones 1-26 was synthesized in two steps and evaluated for their in vitro urease inhibition potential. Results: Out of twenty-six compounds, seventeen have shown good to significant urease inhibitory activity with IC50 values ranging between 49.93-351.46 μM, in comparison to standard thiourea (IC50 = 21 ± 0.11 μM). Moreover, all compounds found to be non-cytotoxic against normal 3T3 cell line. Conclusion: This study has identified β-ketosulfones as novel and non-cytotoxic urease inhibitors.

Photocatalyst-Free Visible Light-Induced Synthesis of β-Oxo Sulfones via Oxysulfonylation of Alkenes with Arylazo Sulfones and Dioxygen in Air

Liu, Qishun,Liu, Fei,Yue, Huilan,Zhao, Xiaohui,Li, Jiangsheng,Wei, Wei

supporting information, p. 5277 - 5282 (2019/11/16)

A catalyst-free strategy has been established for the synthesis of β-oxo sulfones via visible light-induced oxysulfonylation of alkenes with arylazo sulfones with dioxygen in air. The present photoinduced transformation proceeds smoothly at room temperature in the absence of an external photosensitizer, which not only provides a mild and efficient approach to various β-oxo sulfones, but also opens a different reaction mode for the photochemical reaction of arylazo sulfones.

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