24836-02-0

Basic information

• Product Name: 1-CYCLOHEXYL-2,5-DIMETHYL-1H-PYRROLE
• Synonyms: 1H-Pyrrole, 1-cyclohexyl-2,5-dimethyl-
• CAS NO: 24836-02-0
• Molecular Formula: C₁₂H₁₉N
• Molecular Weight: 177.29
• Mol File: 24836-02-0.mol
• Article Data: 35

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-CYCLOHEXYL-2,5-DIMETHYL-1H-PYRROLE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-CYCLOHEXYL-2,5-DIMETHYL-1H-PYRROLE(24836-02-0)
• EPA Substance Registry System: 1-CYCLOHEXYL-2,5-DIMETHYL-1H-PYRROLE(24836-02-0)

Safety Data

• Hazardous Substances Data: 24836-02-0(Hazardous Substances Data)

Usage

Explanation

Different sources of media describe the Explanation of 24836-02-0 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 11 carbon (C) atoms, 17 hydrogen (H) atoms, and 1 nitrogen (N) atom.
2. Heterocyclic compounds are organic compounds with a ring structure containing atoms of different elements. Aromatic compounds are characterized by their stability and delocalized electrons, which give them unique chemical and physical properties.
3. Pyrrole is a type of heterocyclic compound with a five-membered ring containing one nitrogen atom and four carbon atoms. The compound in question belongs to this subclass.
4. The structure of the compound is defined by the arrangement of its atoms. In this case, the compound has a cyclohexyl group attached to the first position of the pyrrole ring, and two methyl groups are attached to the second and fifth positions of the ring.
5. The compound is used in various industries due to its unique chemical properties. It is used in the production of pharmaceuticals, dyes, and as a building block in organic synthesis.
6. The compound can form stable complexes with metal ions, making it useful in coordination chemistry. This property allows it to be used in the development of new drugs and other applications.
7. The compound has potential applications in the pharmaceutical industry for the development of new drugs. It can also be used as a chemical intermediate for the synthesis of various organic compounds.
8. The compound's ability to form stable complexes with metal ions contributes to its stability and makes it a valuable compound in various applications.

Class

Heterocyclic aromatic compound

Subclass

Pyrrole class

Structure

1-Cyclohexyl-2,5-Dimethyl

Applications

Pharmaceutical industry, dyes, organic synthesis

Coordination Chemistry

Acts as a ligand

Potential Applications

Drug development, chemical intermediate

Stability

Forms stable complexes with metal ions

Upstream product

• 2935-44-6 hexane-2,5-diol 
• 108-91-8 cyclohexylamine 
• 110-13-4 2,5-hexanedione 
• 79-24-3 Nitroethane 
• 78-94-4 methyl vinyl ketone 

Downstream Products

• 35711-41-2 1-cyclohexyl-2,5-dimethyl-1H-pyrrole-3-carbaldehyde 
• 920675-87-2 1-(1,3-benzothiazol-2-yl)-1-(1-cyclohexyl-2,5-dimethyl-1H-pyrrol-3-yl)-2,2,2-trifluoroethanol 

Relevant articles and documents

Catalytic activity of the nanoporous MCM-41 surface for the Paal-Knorr pyrrole cyclocondensation

The investigation of different oxide surfaces revealed that nanoporous silica (MCM-41) had the best catalytic activity for Paal-Knorr pyrrole synthesis. Despite the same composition, MCM-41 proved to be more effective than SiO2 itself, probably due to a significantly higher surface area of the SiO2 nanopores. The important features of this "clean" solvent-free protocol are the ease of recovery and the reuse of the catalyst for several cycles, operational simplicity, and easy product isolation and purification.

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

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.

Facile fabrication of porous magnetic covalent organic frameworks as robust platform for multicomponent reaction

The design of cheap yet efficient nanoporous magnetic catalysts for the environmentally benign process's widespread application is an extremely attractive, challenging chemical research field. A novel porous magnetic covalent organic framework was prepared by the condensation reaction of melamine and terephthaladehyde on the surface of 3,4-dihydroxybenzaldehyde coated magnetic Fe3O4 nanoparticles COF@Fe3O4 under hydrothermal conditions for the first time. The high surface area magnetic COF could exhibit superior catalytic activity for sustainable synthesis of trisubstituted and tetrasubstituted imidazoles and pyrroles in good to excellent yields in PEG as solvent under environmentally friendly, ambient conditions and making the overall process economical, efficient, and green. The retrievable catalyst in PEG is general and applicable to a broad substrate scope and functional group compatibility. The structure and morphology of the COF@Fe3O4 were characterized by FTIR, XRD, EDX, and SEM spectroscopy. The COF@Fe3O4 magnetic catalyst was recovered by an external magnet and used for several cycles without significant catalytic activity loss.