13219-97-1 Usage
Description
1-(2-methyl-5-phenyl-1H-pyrrol-3-yl)ethanone is a chemical compound characterized by the molecular formula C13H13NO. It is a derivative of pyrrole, which is a five-membered aromatic heterocycle containing a nitrogen atom. 1-(2-methyl-5-phenyl-1H-pyrrol-3-yl)ethanone is recognized for its potential applications in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, as well as its biological activities such as antifungal and antibacterial properties. Its unique structure and properties make it a valuable compound in the fields of medicinal chemistry and organic synthesis.
Uses
Used in Pharmaceutical Synthesis:
1-(2-methyl-5-phenyl-1H-pyrrol-3-yl)ethanone is used as a key building block in the pharmaceutical industry for the synthesis of various drugs. Its unique structure allows for the creation of a wide range of medicinal compounds with diverse therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 1-(2-methyl-5-phenyl-1H-pyrrol-3-yl)ethanone serves as an essential component in the development of new pesticides and other agricultural chemicals. Its incorporation into these products can enhance their effectiveness and target specific pests or diseases.
Used in Organic Synthesis:
1-(2-methyl-5-phenyl-1H-pyrrol-3-yl)ethanone is utilized as an intermediate in organic synthesis, allowing for the creation of a variety of organic compounds with different properties and applications. Its versatility makes it a valuable asset in the development of new materials and chemicals.
Used in Medicinal Chemistry Research:
Due to its potential biological activities, including antifungal and antibacterial properties, 1-(2-methyl-5-phenyl-1H-pyrrol-3-yl)ethanone is employed in medicinal chemistry research. Scientists use this compound to explore new avenues for drug discovery and to develop novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 13219-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,1 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13219-97:
(7*1)+(6*3)+(5*2)+(4*1)+(3*9)+(2*9)+(1*7)=91
91 % 10 = 1
So 13219-97-1 is a valid CAS Registry Number.
13219-97-1Relevant articles and documents
I2-DMSO promoted metal free oxidative cyclization for the synthesis of substituted Indoles and pyrroles
Ramakrishnam Raju, Addada,Venkata Reddy, Regalla,Mallikarjuna Rao, Vajja,Venkata Naresh, Vema,Venkateswara Rao, Anna
, p. 2838 - 2841 (2016/06/14)
A series of di substituted indole and tri substituted pyrrole derivatives were synthesized efficiently by using I2/K2CO3 in DMSO. The novel synthesis method offers the advantage of mild reaction conditions, operational simplicity, higher yields. The method is functional group tolerant and provides quick access to medicinally significant compounds in moderate to high yields.
Microwave-assisted facile synthesis of trisubstituted pyrrole derivatives
Hanuman Reddy,Mallikarjuna Reddy,Thirupalu Reddy,Rami Reddy
, p. 9805 - 9815 (2015/03/14)
We report efficient synthesis of pyrrole derivatives by use of microwave irradiation. Quantitative yields were obtained in short reaction times. Low yields of product were obtained from alicyclic amino unsaturated ketone derivatives; higher yields were ob
Multicomponent approach towards the synthesis of substituted pyrroles under supramolecular catalysis using β-cyclodextrin as a catalyst in water under neutral conditions
Murthy, Sabbavarapu Narayana,Madhav, Bandaru,Kumar, Akkiligunta Vijay,Rao, Kakulapati Rama,Nageswar, Yadavalli Venkata Durga
experimental part, p. 2118 - 2124 (2009/12/26)
Synthesis of substituted pyrroles in H2O by using β-cyclodextrin as a supramolecular catalyst is described. This reaction has several advantages over existing methods and provides substituted pyrroles in good-to-excellent yields (79-89%). The s
