92596-42-4 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 13 carbon (C) atoms, 15 hydrogen (H) atoms, and 1 nitrogen (N) atom.
Explanation
A pyrrole derivative is a chemical compound that is derived from the parent compound pyrrole, which is a five-membered aromatic heterocycle containing one nitrogen atom.
Explanation
The compound has a five-membered ring structure with alternating single and double bonds, which is characteristic of aromatic heterocycles.
Explanation
The compound contains two methyl groups (-CH3) attached to the pyrrole ring at positions 2 and 5, and a 3,4-dimethylphenyl group (a phenyl group with two methyl groups at positions 3 and 4) attached at position 1.
Explanation
The compound is used in various fields due to its versatile chemical structure, which can be utilized in the development of new drugs, agrochemicals, and materials with specific properties.
Explanation
The compound has been studied for its potential in the preparation of organic semiconductors, which are materials that can conduct electricity and have applications in electronic devices. Additionally, it can be used as a building block for the synthesis of biologically active molecules, which may have therapeutic or other beneficial properties.
Explanation
The compound's structure is defined by the arrangement of its atoms and functional groups. In this case, the structure consists of a pyrrole ring with two methyl groups at positions 2 and 5, and a 3,4-dimethylphenyl group attached at position 1.
Type of Compound
Pyrrole derivative
Aromatic Heterocycle
Five-membered
Functional Groups
Methyl groups and a 3,4-dimethylphenyl group
Applications
Pharmaceutical, agrochemical, and materials science
Potential Uses
Organic semiconductors and synthesis of biologically active molecules
Chemical Structure
1-(3,4-Dimethyl-phenyl)-2,5-dimethyl-1H-pyrrole
Check Digit Verification of cas no
The CAS Registry Mumber 92596-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,9 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92596-42:
(7*9)+(6*2)+(5*5)+(4*9)+(3*6)+(2*4)+(1*2)=164
164 % 10 = 4
So 92596-42-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H17N/c1-10-5-8-14(9-11(10)2)15-12(3)6-7-13(15)4/h5-9H,1-4H3
92596-42-4Relevant articles and documents
Synthesis of Fe3O4@L-proline@SO3H as a novel and reusable acidic magnetic nanocatalyst and its application for the synthesis of N-substituted pyrroles at room temperature under ultrasonic irradiation and without solvent
Behbahani, Farahnaz K.,Shokri, Fatemeh
, (2021/08/18)
N-Substituted pyrroles have been prepared in high isolated yields (65–90%) by the reaction of hexane-2,5-dione with amines or diamines in the presence of Fe3O4@L-proline@SO3H at ambient temperature under ultrasonic irradiation and without solvent. The experimental procedure involves simple operations, and the products are readily separated by external magnet. The same reaction of hexane-2,5-dione with amines containing electron-acceptor substituents, such as 4-nitroaniline, resulted in fair yields of pyrrole derivatives.
Nanomagnetically modified sulfuric acid (γ-Fe2O 3@SiO2-OSO3H): An efficient, fast, and reusable catalyst for greener Paal-Knorr pyrrole synthesis
Cheraghi, Samaneh,Saberi, Dariush,Heydari, Akbar
, p. 1339 - 1343 (2014/07/21)
Paal-Knorr pyrrole synthesis was performed in the presence of superparamagnetic nanoparticles of modified sulfuric acid (γ-Fe 2O3@SiO2-OSO3H) as an efficient and magnetically separable catalyst. Recovery of the catalyst was simple using a magnet, allowing its reuse without significant loss of its catalytic activity (over five cycles).
