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13219-97-1

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13219-97-1 Usage

General Description

1-(2-methyl-5-phenyl-1H-pyrrol-3-yl)ethanone is a chemical compound with the molecular formula C13H13NO. It is a ketone derivative of pyrrole, a five-membered aromatic heterocycle with a nitrogen atom. 1-(2-methyl-5-phenyl-1H-pyrrol-3-yl)ethanone is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its potential biological activities, including antifungal and antibacterial properties. Due to its unique structure and properties, 1-(2-methyl-5-phenyl-1H-pyrrol-3-yl)ethanone is of significant interest in the fields of medicinal chemistry and organic synthesis.

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.

13219-97-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-Methyl-5-phenyl-1H-pyrrol-3-yl)ethanone

1.2 Other means of identification

Product number -
Other names 4-acetyl-5-methyl-2-phenylpyrrole

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:13219-97-1 SDS

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

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