Cas no 35695-49-9 (cyano(propan-2-yl)amine)

Cyano(propan-2-yl)amine is a versatile organic compound featuring both cyano and secondary amine functional groups, making it valuable in synthetic chemistry applications. Its structure allows for reactivity in nucleophilic additions and condensation reactions, serving as a precursor for pharmaceuticals, agrochemicals, and specialty chemicals. The compound's stability under standard conditions and compatibility with a range of solvents enhance its utility in multi-step synthesis. Its moderate polarity and balanced steric properties facilitate selective transformations, while the cyano group offers further derivatization potential. Cyano(propan-2-yl)amine is particularly useful in heterocycle formation and as an intermediate in fine chemical production.
cyano(propan-2-yl)amine structure
cyano(propan-2-yl)amine structure
Product Name:cyano(propan-2-yl)amine
CAS No:35695-49-9
MF:C4H8N2
MW:84.1197204589844
MDL:MFCD16767884
CID:1472271
PubChem ID:12295217
Update Time:2025-06-08

cyano(propan-2-yl)amine Chemical and Physical Properties

Names and Identifiers

    • Cyanamide, (1-methylethyl)-
    • N-isopropylcyanamide
    • cyano(propan-2-yl)amine
    • EN300-246283
    • GYEOFMXQZPOQIX-UHFFFAOYSA-N
    • 35695-49-9
    • isopropyl cyanamide
    • AKOS011772990
    • MDL: MFCD16767884
    • Inchi: 1S/C4H8N2/c1-4(2)6-3-5/h4,6H,1-2H3
    • InChI Key: GYEOFMXQZPOQIX-UHFFFAOYSA-N
    • SMILES: N(C#N)C(C)C

Computed Properties

  • Exact Mass: 84.06884
  • Monoisotopic Mass: 84.068748264g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 6
  • Rotatable Bond Count: 1
  • Complexity: 66.9
  • 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: 1.2
  • Topological Polar Surface Area: 35.8?2

Experimental Properties

  • PSA: 35.82

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Additional information on cyano(propan-2-yl)amine

Comprehensive Overview of Cyano(propan-2-yl)amine (CAS No. 35695-49-9): Properties, Applications, and Industry Insights

Cyano(propan-2-yl)amine (CAS No. 35695-49-9), also known as isopropyl cyanamide, is a versatile organic compound with significant relevance in pharmaceutical, agrochemical, and specialty chemical industries. Its molecular structure, featuring a cyano group (–C≡N) bonded to an isopropylamine moiety, enables unique reactivity and functional utility. This article delves into its physicochemical properties, synthesis pathways, applications, and emerging trends aligned with current industry demands, such as green chemistry and sustainable synthesis.

The compound’s molecular formula, C4H8N2, and molecular weight of 84.12 g/mol make it a lightweight yet reactive intermediate. Its boiling point (approximately 120–125°C) and solubility in polar solvents like ethanol and water facilitate its integration into diverse reaction systems. Researchers frequently explore cyano(propan-2-yl)amine for N-heterocycle synthesis, a critical process in drug development, owing to its ability to act as a nitrile precursor or amine donor.

In the pharmaceutical sector, CAS No. 35695-49-9 is valued for its role in constructing bioactive scaffolds. For instance, it serves as a building block for antiviral agents and kinase inhibitors, addressing global health challenges like emerging infectious diseases. Recent studies highlight its potential in covalent inhibitor design, a trending topic in targeted cancer therapies. These applications align with the growing demand for precision medicine, a frequently searched term in scientific databases.

Agrochemical innovations also leverage cyano(propan-2-yl)amine for developing crop protection agents. Its incorporation into herbicide and pesticide formulations enhances efficacy while meeting environmental regulations. This resonates with the sustainable agriculture movement, a hot topic among policymakers and farmers. Notably, the compound’s degradability profile is under scrutiny to ensure compliance with EPA and REACH standards, addressing concerns about chemical persistence in ecosystems.

From a synthetic perspective, isopropyl cyanamide is often prepared via nucleophilic substitution reactions between isopropylamine and cyanogen bromide. Modern flow chemistry techniques are being adopted to improve yield and safety, reflecting the industry’s shift toward continuous manufacturing. Such advancements cater to the rising interest in process intensification, a keyword dominating chemical engineering forums.

Quality control of CAS No. 35695-49-9 involves HPLC and GC-MS analyses to verify purity, a critical factor for end-users. Storage recommendations typically include anhydrous conditions and inert atmospheres to prevent hydrolysis of the cyano group. These protocols are frequently discussed in chemical handling guides, a common search query among laboratory professionals.

Emerging research explores the compound’s utility in material science, particularly in polymeric coatings and adhesives. Its dual functionality allows crosslinking reactions, enhancing material durability—a sought-after property in automotive and aerospace applications. This intersects with the booming interest in high-performance materials, a trending topic in R&D circles.

In summary, cyano(propan-2-yl)amine (CAS No. 35695-49-9) is a multifaceted compound bridging gaps between organic synthesis, pharmaceuticals, and agrochemicals. Its adaptability to green chemistry principles and alignment with industry 4.0 trends ensure its continued relevance. As demand grows for specialty chemicals and custom intermediates, this compound remains a focal point for innovation, answering pressing questions in drug discovery and sustainable manufacturing.

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