299426-84-9 Usage
Description
1-(2-ETHYL-PHENYL)-1H-PYRROLE, also known as 2-ethyl-phenylpyrrole, is a chemical compound with the molecular formula C13H15N. It is a derivative of pyrrole, a five-membered heterocyclic compound containing a nitrogen atom in the ring. 1-(2-ETHYL-PHENYL)-1H-PYRROLE is recognized for its potential applications in various industries, particularly in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Its study also extends to potential biological activities, such as antifungal properties and the treatment of neurodegenerative diseases, making it a significant molecule in the field of organic chemistry.
Uses
Used in Pharmaceutical Industry:
1-(2-ETHYL-PHENYL)-1H-PYRROLE is used as a building block for the synthesis of various pharmaceuticals. Its unique molecular structure allows for the creation of a wide range of drugs with different therapeutic applications, contributing to the development of new treatments for various health conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(2-ETHYL-PHENYL)-1H-PYRROLE is utilized as a component in the development of new agrochemicals. Its incorporation into these products can enhance their effectiveness in protecting crops from pests and diseases, thereby increasing agricultural productivity.
Used as an Antifungal Agent:
1-(2-ETHYL-PHENYL)-1H-PYRROLE is used as an antifungal agent due to its potential biological activities. It can be employed in the development of treatments for fungal infections, providing a new avenue for combating these diseases and improving patient outcomes.
Used in the Treatment of Neurodegenerative Diseases:
1-(2-ETHYL-PHENYL)-1H-PYRROLE is also being studied for its potential use in the treatment of neurodegenerative diseases. Its incorporation into new drug formulations could lead to the development of more effective therapies for conditions such as Alzheimer's, Parkinson's, and other related diseases, offering hope for patients and their families.
Check Digit Verification of cas no
The CAS Registry Mumber 299426-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,4,2 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 299426-84:
(8*2)+(7*9)+(6*9)+(5*4)+(4*2)+(3*6)+(2*8)+(1*4)=199
199 % 10 = 9
So 299426-84-9 is a valid CAS Registry Number.
299426-84-9Relevant articles and documents
Nickel-Catalyzed Synthesis of N-Substituted Pyrroles Using Diols with Aryl- and Alkylamines
Singh, Khushboo,Kabadwal, Lalit Mohan,Bera, Sourajit,Alanthadka, Anitha,Banerjee, Debasis
, p. 15406 - 15414 (2019/01/04)
Herein, nickel-catalyzed sustainable strategy for the synthesis of N-substituted pyrroles using butene-1,4-diols and butyne-1,4-diols with a series of aryl-, alkyl-, and heteroarylamines is reported. The catalytic protocol is tolerant of free alcohol, halide, alkyl, alkoxy, oxygen heterocycles, activated benzyl, and the pyridine moiety and resulted in up to 90% yield. Initial mechanistic studies involving defined nickel catalyst, determination of rate, and order of reaction including deuterium-labeling experiments were performed for pyrrole synthesis.
Nano sulfated titania as a heterogeneous solid acid catalyst for the synthesis of pyrroles by clauson-kaas condensation under solvent-free conditions
Hosseini-Sarvari,Najafvand-Derikvandi,Jarrahpour,Heiran
, p. 1732 - 1739 (2014/05/06)
A new and environmentally benign method for the preparation of N-substituted pyrroles from one-pot condensation reaction of 2,5-dimethoxytetrahydrofuran with amines and diamines in the presence of nano sulfated titania under solvent-free conditions is presented. This new protocol features simple operation, easy availability, stability, and eco-friendliness of catalyst, as well as high to excellent yields of products. In addition, we report for the first time an alternative method for the synthesis of pyrroles from aromatic amines containing the β-lactam fragment using nano sulfated titania as catalyst.
