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"2(1H)-Pyridinone, 1-[(phenylsulfonyl)oxy]-" is a chemical compound with the molecular formula C11H9NO3S. It is a derivative of 2-pyridinone, featuring a phenylsulfonyl group attached to the oxygen atom at the 1-position. 2(1H)-Pyridinone, 1-[(phenylsulfonyl)oxy]- is known for its potential applications in organic synthesis and as an intermediate in the preparation of various pharmaceuticals and agrochemicals. Its structure provides a unique combination of a pyridinone ring and a phenylsulfonyl group, which can participate in various chemical reactions, such as nucleophilic substitutions and eliminations, making it a versatile building block in the synthesis of more complex molecules.

5033-19-2

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5033-19-2 Usage

General Description

2(1H)-Pyridinone, 1-[(phenylsulfonyl)oxy]- is a chemical compound with the molecular formula C11H9NO4S. It is a pyridinone derivative with a sulfonyl group attached to the oxygen atom. 2(1H)-Pyridinone, 1-[(phenylsulfonyl)oxy]- has potential applications in the field of pharmaceuticals and organic synthesis, as it can be used as a building block in the synthesis of various bioactive molecules. It has been studied for its potential as an anti-inflammatory and anti-cancer agent, and its unique structural properties make it a valuable tool for medicinal chemistry research. Additionally, the sulfonyl group attached to the oxygen atom can provide added reactivity and selectivity in chemical reactions, making 2(1H)-Pyridinone, 1-[(phenylsulfonyl)oxy]- a versatile tool for synthetic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 5033-19-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,3 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5033-19:
(6*5)+(5*0)+(4*3)+(3*3)+(2*1)+(1*9)=62
62 % 10 = 2
So 5033-19-2 is a valid CAS Registry Number.

5033-19-2SDS

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 2-oxopyridin-1(2H)-yl benzenesulfonate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5033-19-2 SDS

5033-19-2Relevant academic research and scientific papers

Activation of sulfonate ester based matrix metalloproteinase proinhibitors by hydrogen peroxide

Daniel, Kevin B.,Major Jourden, Jody L.,Negoescu, Kimberly E.,Cohen, Seth M.

experimental part, p. 313 - 323 (2012/01/13)

This study details the development of matrix metalloproteinase inhibitor prodrugs (proMMPi) that are activated in the presence of reactive-oxygen species (ROS). Conventional matrix metalloproteinase inhibitors (MMPi) utilize a zinc-binding group (ZBG) that chelates to the catalytic zinc(II) ion of matrix metalloproteinases (MMPs) to inhibit their activity. To create ROS-sensitive prodrugs, sulfonate esters were used as a protecting group for the ZBG to block their metal binding ability. Surprisingly, these sulfonate esters were found to be cleaved by H2O2 only when the ZBG contained an N-oxide donor atom moiety. Sulfonate ester derivatives of full-length MMPi based on these ROS-triggerable systems were synthesized. It was found that proMMPi with sulfonate ester protecting groups showed relatively high rates of cleavage in the presence of H2O2 to release the active MMPi. In vitro MMP inhibition studies confirmed a significant increase in inhibitory activity of proMMPi upon addition of H2O2, demonstrating the use of sulfonate esters to act as cleavable triggers for ROS-activated prodrugs.

STIMULUS-TRIGGERED PRODRUGS

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Page/Page column 37, (2012/01/13)

Set forth herein, inter alia, are compositions and methods for treating diseases with prodrugs. Provided herein are prodrug compositions for inhibiting the function of proteins, compositions and methods for treating diseases associated with oxidative compounds, oxidatively-sensitive prodrugs of inhibitors of metalloproteases. and methods of inhibiting metalloproteases using oxidatively-sensitive prodrugs.

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