Cas no 1019586-26-5 (N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline)

N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline is a specialized organic compound featuring a cyclopropyl-substituted ethylamine group and a methylsulfanyl-substituted aromatic ring. This structure imparts unique steric and electronic properties, making it valuable in synthetic chemistry and pharmaceutical research. The cyclopropyl group enhances conformational rigidity, while the methylsulfanyl moiety offers potential for further functionalization. Its balanced lipophilicity and moderate reactivity make it suitable for applications in medicinal chemistry, particularly as an intermediate in the synthesis of bioactive molecules. The compound’s stability under standard conditions ensures reliable handling and storage. Its distinct structural features provide opportunities for tailored modifications in drug discovery and agrochemical development.
N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline structure
1019586-26-5 structure
Product Name:N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline
CAS No:1019586-26-5
MF:C12H17NS
MW:207.33508181572
CID:5156341
PubChem ID:43192270
Update Time:2026-03-04

N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline Chemical and Physical Properties

Names and Identifiers

    • Benzenamine, N-(1-cyclopropylethyl)-4-(methylthio)-
    • n-(1-Cyclopropylethyl)-4-(methylthio)aniline
    • N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline
    • Inchi: 1S/C12H17NS/c1-9(10-3-4-10)13-11-5-7-12(14-2)8-6-11/h5-10,13H,3-4H2,1-2H3
    • InChI Key: BQQOYJPMJVCHCS-UHFFFAOYSA-N
    • SMILES: C1(NC(C2CC2)C)=CC=C(SC)C=C1

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Additional information on N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline

Comprehensive Overview of N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline (CAS No. 1019586-26-5)

N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline (CAS No. 1019586-26-5) is a specialized organic compound that has garnered significant attention in the fields of medicinal chemistry and material science. This compound, characterized by its unique cyclopropyl and methylsulfanyl functional groups, exhibits properties that make it a valuable intermediate in the synthesis of more complex molecules. Researchers and industry professionals are increasingly interested in its potential applications, particularly in drug discovery and agrochemical development.

The molecular structure of N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline features a cyclopropylethyl moiety attached to an aniline ring, which is further substituted with a methylsulfanyl group. This configuration imparts distinct electronic and steric properties, making it a versatile building block in organic synthesis. Recent studies have explored its role in the development of novel pharmaceutical intermediates, where its stability and reactivity are highly prized. The compound's CAS No. 1019586-26-5 serves as a critical identifier for researchers sourcing high-purity samples for experimental purposes.

In the context of current trends, N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline aligns with the growing demand for sustainable chemistry and green synthesis methods. As industries strive to reduce environmental impact, this compound's potential for use in catalysis and biodegradable materials has become a focal point. Additionally, its relevance in AI-driven drug discovery platforms highlights its intersection with cutting-edge technology, a topic frequently searched by professionals in the field.

From a technical standpoint, the synthesis of N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline involves multi-step organic reactions, including amination and thioetherification processes. These methods are well-documented in peer-reviewed journals, ensuring reproducibility for laboratory-scale production. The compound's physicochemical properties, such as solubility and melting point, are critical for its handling and application in various research settings. Analytical techniques like HPLC and NMR spectroscopy are commonly employed to verify its purity and structural integrity.

The commercial availability of N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline (CAS No. 1019586-26-5) is supported by several chemical suppliers, catering to the needs of academic and industrial researchers. Its inclusion in high-throughput screening libraries underscores its importance in modern drug development pipelines. Furthermore, the compound's compatibility with click chemistry and other modular synthesis approaches has expanded its utility in creating diverse molecular architectures.

Looking ahead, the potential applications of N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline are expected to grow, particularly in areas like personalized medicine and smart materials. Its role in the design of targeted therapeutics and functional polymers is an active area of investigation. As the scientific community continues to explore its capabilities, this compound is poised to remain a key player in advancing innovation across multiple disciplines.

In summary, N-(1-cyclopropylethyl)-4-(methylsulfanyl)aniline (CAS No. 1019586-26-5) represents a compelling example of how specialized organic compounds can drive progress in science and technology. Its unique structural features, combined with its broad applicability, make it a subject of enduring interest for researchers and industry leaders alike.

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