132726-51-3 Usage
Explanation
This is the full name of the chemical compound, indicating its structure and components.
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms in the compound.
3. Pyrrole Derivative
Explanation
The compound is derived from the pyrrole structure, which is a five-membered aromatic ring containing one nitrogen atom.
4. 4-Methoxyphenyl Group
Explanation
A methoxy group (-OCH3) is attached to the 4th position of a phenyl ring, which is connected to the first carbon atom of the pyrrole ring.
5. 2-Methyl Group
Explanation
A methyl group (-CH3) is attached to the second carbon atom of the pyrrole ring.
6. 5-Phenyl Group
Explanation
A phenyl group (a benzene ring) is attached to the fifth carbon atom of the pyrrole ring.
Explanation
Due to its unique structure and properties, the compound may be used in the synthesis of pharmaceuticals and other organic compounds.
8. Biological Activity
Explanation
The compound may exhibit biological activity, making it a potential candidate for drug development.
9. Further Research Needed
Explanation
More research is required to fully understand the compound's potential uses and effects.
Potential Applications
Pharmaceuticals and Organic Synthesis
Check Digit Verification of cas no
The CAS Registry Mumber 132726-51-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,2 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 132726-51:
(8*1)+(7*3)+(6*2)+(5*7)+(4*2)+(3*6)+(2*5)+(1*1)=113
113 % 10 = 3
So 132726-51-3 is a valid CAS Registry Number.
132726-51-3Relevant articles and documents
A straightforward highly efficient Paal-Knorr synthesis of pyrroles
Banik, Bimal K.,Banik, Indrani,Renteria, Mercy,Dasgupta, Swapan K.
, p. 2643 - 2645 (2005)
A straightforward simple synthesis of substituted pyrroles using bismuth nitrate-catalyzed modified Paal-Knorr method has been accomplished with an excellent yield. This method produces pyrroles with multicyclic aromatic amines.
A fluorescent target-guided Paal-Knorr reaction
Kornienko, Alexander,La Clair, James J.,Maslivetc, Vladimir,Wagh, Sachin B.
, p. 37035 - 37039 (2020/10/19)
It has become increasingly apparent that high-diversity chemical reactions play a significant role in the discovery of bioactive small molecules. Here, we describe an expanse of this paradigm, combining a ‘target-guided synthesis’ concept with Paal-Knorr chemistry applied to the preparation of fluorescent ligands for human prostaglandin-endoperoxide synthase (COX-2).
One-pot synthesis of 2-methyl-1,5-diaromatic-1H-pyrroles from styrene, acetone and arylamines using TBHP, copper(II) trifluoromethanesulfonate and sulfamic acid
Xu, Congjun,Han, Yufei,Chen, Shaowei,Xu, Dengzhi,Zhang, Bingfu,Shan, Zhenliang,Du, Shimei,Xu, Liying,Gong, Ping
, p. 260 - 263 (2017/12/29)
The one-pot copper/manganese co-catalyzed heterocyclization of arylamine derivatives with styrene and acetone to produce a series of 2-methyl-1,5-diaromatic-1H-pyrroles was investigated. The described reaction combines 1,4-dicarbonyl synthesis and Paal-Knorr type condensation reactions.
