124511-96-2 Usage
Uses
Used in Organic Synthesis:
3-(Chloroacetyl)-1-tosylpyrrole is used as a building block for the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with different functional groups, making it a valuable component in the development of new organic materials.
Used in Coordination Chemistry:
In coordination chemistry, 3-(Chloroacetyl)-1-tosylpyrrole serves as a ligand, which can bind to metal ions to form coordination complexes. These complexes have potential applications in areas such as catalysis, materials science, and supramolecular chemistry.
Used in Pharmaceutical Synthesis:
3-(Chloroacetyl)-1-tosylpyrrole is used as a potential precursor for the synthesis of biologically active molecules and pharmaceuticals. Its unique structure and functional groups make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry Research:
3-(Chloroacetyl)-1-tosylpyrrole has been investigated for its potential use as a reagent in the preparation of other functionalized pyrrole derivatives. Its biological activity and potential applications in medicinal chemistry research make it an interesting compound for further study and development.
Used in the Preparation of Functionalized Pyrrole Derivatives:
3-(Chloroacetyl)-1-tosylpyrrole is utilized as a reagent for the synthesis of other functionalized pyrrole derivatives. These derivatives can have various applications in different fields, such as pharmaceuticals, materials science, and chemical 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.
124511-96-2Relevant academic research and scientific papers
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.
3-substituted polypyrrole
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, (2008/06/13)
There is provided a 3-substituted polypyrrole represented by the general formula (I) STR1 wherein R is an alkyl group having 1 to 5 carbon atoms, m is an integer of from 1 to 20, and n is an integer of 2 or more.
