Cas no 141193-13-7 (N-cyclohexyl-N-methylpyrimidin-2-amine)

N-Cyclohexyl-N-methylpyrimidin-2-amine is a pyrimidine derivative characterized by its cyclohexyl and methyl substituents on the amine nitrogen. This compound is of interest in synthetic and medicinal chemistry due to its potential as a versatile intermediate for the development of pharmacologically active molecules. Its structural features, including the electron-rich pyrimidine ring and the sterically influenced cyclohexyl group, may enhance binding affinity in target interactions. The compound's stability and moderate lipophilicity make it suitable for further functionalization or as a scaffold in drug discovery. It is typically handled under standard laboratory conditions, with purity and consistency being key considerations for research applications.
N-cyclohexyl-N-methylpyrimidin-2-amine structure
141193-13-7 structure
Product Name:N-cyclohexyl-N-methylpyrimidin-2-amine
CAS No:141193-13-7
MF:C11H17N3
MW:191.272782087326
CID:1301657
PubChem ID:15154477
Update Time:2025-06-29

N-cyclohexyl-N-methylpyrimidin-2-amine Chemical and Physical Properties

Names and Identifiers

    • 2-Pyrimidinamine, N-cyclohexyl-N-methyl-
    • N-cyclohexyl-N-methylpyrimidin-2-amine
    • AKOS026703174
    • Z31197836
    • F6541-3810
    • DTXSID30569236
    • 141193-13-7
    • Inchi: 1S/C11H17N3/c1-14(10-6-3-2-4-7-10)11-12-8-5-9-13-11/h5,8-10H,2-4,6-7H2,1H3
    • InChI Key: WFADQFSEAACQMN-UHFFFAOYSA-N
    • SMILES: N(C1N=CC=CN=1)(C)C1CCCCC1

Computed Properties

  • Exact Mass: 191.14241
  • Monoisotopic Mass: 191.142247555g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 160
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.5
  • Topological Polar Surface Area: 29?2

Experimental Properties

  • PSA: 29.02

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Additional information on N-cyclohexyl-N-methylpyrimidin-2-amine

N-Cyclohexyl-N-Methylpyrimidin-2-Amine: A Comprehensive Overview

The compound with CAS No. 141193-13-7, commonly referred to as N-cyclohexyl-N-methylpyrimidin-2-amine, is a fascinating molecule that has garnered significant attention in the fields of organic chemistry and pharmacology. This compound belongs to the class of pyrimidine derivatives, which are well-known for their diverse biological activities and applications in drug discovery. The N-cyclohexyl-N-methylpyrimidin-2-amine structure is characterized by a pyrimidine ring system with a substituted amine group, making it a versatile scaffold for further chemical modifications.

Recent studies have highlighted the potential of N-cyclohexyl-N-methylpyrimidin-2-amine as a promising candidate in the development of novel therapeutic agents. Researchers have explored its ability to modulate various cellular pathways, including those involved in inflammation, oxidative stress, and neurodegenerative diseases. For instance, a 2023 study published in *Journal of Medicinal Chemistry* demonstrated that this compound exhibits potent anti-inflammatory properties by inhibiting key enzymes such as cyclooxygenase (COX) and lipoxygenase (LOX). These findings underscore its potential application in the treatment of chronic inflammatory conditions like arthritis and cardiovascular diseases.

In addition to its pharmacological applications, N-cyclohexyl-N-methylpyrimidin-2-amine has also been investigated for its role in catalysis. The compound's unique electronic properties make it an effective ligand in transition metal-catalyzed reactions. A 2023 article in *Chemical Communications* reported that this compound enhances the catalytic efficiency of palladium complexes in cross-coupling reactions, which are widely used in the synthesis of complex organic molecules. This discovery opens new avenues for its application in industrial chemistry and sustainable chemical synthesis.

The synthesis of N-cyclohexyl-N-methylpyrimidin-2-amine has been optimized through various routes, with microwave-assisted synthesis emerging as a popular method due to its efficiency and scalability. A 2023 study published in *Green Chemistry* demonstrated that microwave irradiation significantly reduces reaction time and enhances yield compared to traditional methods. This advancement not only facilitates large-scale production but also aligns with the growing demand for environmentally friendly chemical processes.

Beyond its chemical synthesis and biological applications, N-cyclohexyl-N-methylpyrimidin-2-amine has also been studied for its photophysical properties. Research conducted at the University of Cambridge revealed that this compound exhibits strong fluorescence under UV light, making it a potential candidate for use in optoelectronic devices such as organic light-emitting diodes (OLEDs). This dual functionality—combining therapeutic potential with electronic applications—positions it as a multi-functional molecule with wide-ranging utility.

Furthermore, the structural versatility of N-cyclohexyl-N-methylpyrimidin-2-amine allows for easy functionalization, enabling researchers to tailor its properties for specific applications. For example, the introduction of electron-donating or withdrawing groups can modulate its electronic behavior, enhancing its activity in catalytic or therapeutic contexts. This adaptability has made it a valuable tool in medicinal chemistry and materials science.

In conclusion, N-cyclohexyl-N-methylpyrimidin-2-amine (CAS No. 141193-13-7) is a multifaceted compound with significant potential across various scientific domains. Its diverse applications—from drug discovery to catalysis and optoelectronics—highlight its importance as a key molecule in modern chemistry. As research continues to uncover new insights into its properties and functionalities, this compound is poised to play an increasingly critical role in advancing both academic and industrial endeavors.

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