Cas no 36567-15-4 (1-(Ethylsulfanyl)-2-isocyanatopropane)

1-(Ethylsulfanyl)-2-isocyanatopropane is a sulfur-containing isocyanate compound characterized by its reactive isocyanate functional group and ethylthio side chain. This structure imparts unique reactivity, making it suitable for applications in organic synthesis, particularly in the preparation of thiourethanes and other sulfur-functionalized polymers. The ethylthio group enhances solubility in nonpolar solvents, facilitating its use in hydrophobic systems. Its isocyanate group enables efficient crosslinking with hydroxyl or amine groups, contributing to the formation of durable polymeric materials. The compound is typically handled under controlled conditions due to its moisture sensitivity and potential reactivity. It serves as a valuable intermediate in specialty chemical synthesis and material science research.
1-(Ethylsulfanyl)-2-isocyanatopropane structure
36567-15-4 structure
Product Name:1-(Ethylsulfanyl)-2-isocyanatopropane
CAS No:36567-15-4
MF:C6H11NOS
MW:145.222640275955
CID:5932149
PubChem ID:112704022
Update Time:2025-11-02

1-(Ethylsulfanyl)-2-isocyanatopropane Chemical and Physical Properties

Names and Identifiers

    • EN300-1826206
    • 36567-15-4
    • 1-(ethylsulfanyl)-2-isocyanatopropane
    • 1-(Ethylsulfanyl)-2-isocyanatopropane
    • Inchi: 1S/C6H11NOS/c1-3-9-4-6(2)7-5-8/h6H,3-4H2,1-2H3
    • InChI Key: FYAFIHKKGHKXPX-UHFFFAOYSA-N
    • SMILES: S(CC)CC(C)N=C=O

Computed Properties

  • Exact Mass: 145.05613515g/mol
  • Monoisotopic Mass: 145.05613515g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 4
  • Complexity: 110
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.4
  • Topological Polar Surface Area: 54.7?2

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Additional information on 1-(Ethylsulfanyl)-2-isocyanatopropane

Comprehensive Guide to 1-(Ethylsulfanyl)-2-isocyanatopropane (CAS No. 36567-15-4): Properties, Applications, and Industry Insights

1-(Ethylsulfanyl)-2-isocyanatopropane (CAS 36567-15-4) is a specialized organic compound that has garnered significant attention in industrial and research applications. This molecule, characterized by its ethylsulfanyl and isocyanate functional groups, plays a pivotal role in synthetic chemistry and material science. With the growing demand for high-performance chemicals, understanding the properties and applications of 1-(Ethylsulfanyl)-2-isocyanatopropane is essential for professionals in pharmaceuticals, coatings, and polymer industries.

The chemical structure of 1-(Ethylsulfanyl)-2-isocyanatopropane features a reactive isocyanate group (-NCO) and a sulfur-containing ethylsulfanyl moiety (-SC?H?). This combination enables versatile reactivity, making it valuable for cross-linking reactions, polymerization, and surface modification. Researchers often explore its potential in creating advanced materials with tailored properties, such as improved adhesion, thermal stability, or chemical resistance.

One of the most searched questions about 1-(Ethylsulfanyl)-2-isocyanatopropane is its role in polyurethane synthesis. As industries shift toward sustainable practices, this compound is being investigated for eco-friendly formulations. Its ability to form urethane linkages under mild conditions aligns with the global push for greener chemistry. Additionally, its ethylsulfanyl group offers unique opportunities for functionalization, which is a hot topic in drug discovery and agrochemical development.

From an industrial perspective, CAS 36567-15-4 is often utilized in specialty coatings and adhesives. The compound’s reactivity allows it to serve as a building block for high-performance polymers, which are in high demand for automotive, aerospace, and electronics applications. Recent studies also highlight its potential in self-healing materials, a cutting-edge area that attracts significant R&D investment.

Safety and handling of 1-(Ethylsulfanyl)-2-isocyanatopropane are frequently discussed in professional forums. While not classified as a hazardous material under standard regulations, proper storage and handling protocols are recommended to maintain stability. Users often search for compatible solvents and reaction conditions, emphasizing the need for clear technical guidelines.

Market trends indicate a rising demand for isocyanate derivatives, including 1-(Ethylsulfanyl)-2-isocyanatopropane, driven by advancements in material science and biotechnology. Companies are increasingly focusing on scalable synthesis methods to meet industrial needs while minimizing environmental impact. This aligns with broader industry movements toward circular economy principles and reduced carbon footprints.

In summary, 1-(Ethylsulfanyl)-2-isocyanatopropane (CAS 36567-15-4) is a versatile compound with wide-ranging applications. Its unique chemical properties make it indispensable in modern synthetic chemistry, while ongoing research continues to uncover new possibilities. For professionals seeking reliable data on this compound, understanding its structure, reactivity, and industrial relevance is crucial for innovation and compliance with evolving regulatory standards.

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