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124511-96-2

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124511-96-2 Usage

General Description

3-(Chloroacetyl)-1-tosylpyrrole is a chemical compound with the molecular formula C13H11ClNO3S. It is a pyrrole derivative with a tosyl (tosylate) group and a chloroacetyl substituent. 3-(CHLOROACETYL)-1-TOSYLPYRROLE has a range of potential applications, including as a building block in organic synthesis and as a ligand in coordination chemistry. It is also a potential precursor for the synthesis of biologically active molecules and pharmaceuticals. Additionally, 3-(Chloroacetyl)-1-tosylpyrrole has been investigated for its potential use as a reagent in the preparation of other functionalized pyrrole derivatives and for its biological activity in medicinal chemistry research.

Check Digit Verification of cas no

The CAS Registry Mumber 124511-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,1 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 124511-96:
(8*1)+(7*2)+(6*4)+(5*5)+(4*1)+(3*1)+(2*9)+(1*6)=102
102 % 10 = 2
So 124511-96-2 is a valid CAS Registry Number.

124511-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-[1-(4-methylphenyl)sulfonylpyrrol-3-yl]ethanone

1.2 Other means of identification

Product number -
Other names 3-chloroacetyl-N-tosylpyrrole

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:124511-96-2 SDS

124511-96-2Relevant articles and documents

Synthesis of novel pyrrolyl-indomethacin derivatives

Serra Moreno, Judith,Agas, Dimitrios,Sabbieti, Maria Giovanna,Di Magno, Matteo,Migliorini, Antonella,Loreto, M. Antonietta

, p. 391 - 397 (2013/01/15)

In the present work, we report the synthesis of the novel esters of indomethacin (IDMC) and an ester of reduced IDMC. For this purpose, IDMC is covalently bound by using a spacer chain to the pyrrole (Py) in the 3-position. The innovative pyrrole-indomethacin (3-Py-IDMC) derivates show no cytotoxic effects in primary calvarial osteoblasts. The designed IDMC derivates have been studied because they could be injected locally as a component of polymeric micro-particles. In fact, the new 3-Py-IDMC derivatives will assure their further polymerization since the 2- and 5-monomer positions are free.

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