Cas no 66892-01-1 ((2-methylprop-2-en-1-yl)thiourea)

(2-Methylprop-2-en-1-yl)thiourea is a thiourea derivative featuring a reactive allylic group, making it a versatile intermediate in organic synthesis and polymer chemistry. Its structure combines the nucleophilic properties of the thiourea moiety with the electrophilic reactivity of the allyl group, enabling applications in crosslinking, polymerization, and functionalization reactions. The compound is particularly useful in the preparation of thiourea-based resins, adhesives, and coatings, where it enhances thermal stability and mechanical properties. Its dual functionality also allows for use in pharmaceutical and agrochemical synthesis as a building block for bioactive molecules. The product is typically handled under controlled conditions due to its potential reactivity.
(2-methylprop-2-en-1-yl)thiourea structure
66892-01-1 structure
Product Name:(2-methylprop-2-en-1-yl)thiourea
CAS No:66892-01-1
MF:C5H10N2S
MW:130.211299419403
CID:523855
PubChem ID:4538125
Update Time:2025-07-01

(2-methylprop-2-en-1-yl)thiourea Chemical and Physical Properties

Names and Identifiers

    • Thiourea,N-(2-methyl-2-propen-1-yl)-
    • 2-methylprop-2-enylthiourea
    • (2-methylprop-2-en-1-yl)thiourea
    • AC1NCR26
    • AC1Q1J6X
    • EN300-66366
    • Methallyl-thioharnstoff
    • methallylthiourea
    • methallyl-thiourea
    • N-(2-methylprop-2-en-1-yl)thiourea
    • NSC172998
    • 66892-01-1
    • CS-0257165
    • SCHEMBL4523707
    • DTXSID10404055
    • NSC-172998
    • AKOS006239347
    • Inchi: 1S/C5H10N2S/c1-4(2)3-7-5(6)8/h1,3H2,2H3,(H3,6,7,8)
    • InChI Key: ZWANTMRZNYWRIK-UHFFFAOYSA-N
    • SMILES: S=C(N)NCC(=C)C

Computed Properties

  • Exact Mass: 130.0566
  • Monoisotopic Mass: 130.056
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 2
  • Complexity: 109
  • 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
  • Topological Polar Surface Area: 70.1A^2
  • XLogP3: 0.8

Experimental Properties

  • Density: 1.054
  • Boiling Point: 204.2°Cat760mmHg
  • Flash Point: 77.3°C
  • Refractive Index: 1.547
  • PSA: 38.05
  • LogP: 1.48690

(2-methylprop-2-en-1-yl)thiourea Pricemore >>

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Additional information on (2-methylprop-2-en-1-yl)thiourea

(2-Methylprop-2-en-1-yl)Thiourea: A Comprehensive Overview

Thioureas are a class of organic compounds that have garnered significant attention in the fields of chemistry, materials science, and pharmacology due to their versatile properties and wide-ranging applications. Among these, (2-methylprop-2-en-1-yl)thiourea, with the CAS number 66892-01-1, stands out as a compound of particular interest. This article delves into the structural characteristics, synthesis methods, and recent advancements in the application of this compound.

The molecular structure of (2-methylprop-2-en-1-yl)thiourea is defined by its unique arrangement of atoms. The compound consists of a thiourea group (-NCS-) attached to a substituted propene moiety. The thiourea functional group is known for its ability to coordinate with metal ions, making it a valuable component in catalysis and material synthesis. Recent studies have highlighted the potential of this compound in stabilizing metal nanoparticles, which could revolutionize its use in catalytic processes.

One of the most intriguing aspects of (2-methylprop-2-en-1-yl)thiourea is its role in organic synthesis. Researchers have demonstrated that this compound can act as a versatile building block for constructing complex organic molecules. For instance, it has been employed in the synthesis of heterocyclic compounds, which are crucial in drug discovery and agrochemical development. The ability of this compound to undergo various transformations under mild conditions has made it a favorite among synthetic chemists.

Recent advancements in green chemistry have also brought (2-methylprop-2-en-1-yl)thiourea into the spotlight. Scientists have explored its use as a sustainable reagent in eco-friendly synthetic protocols. For example, it has been utilized in the development of biodegradable polymers, which hold immense potential in reducing environmental pollution. These findings underscore the compound's role in promoting sustainable chemical practices.

The application of (2-methylprop-2-en-1-yl)thiourea extends beyond traditional chemistry into the realm of materials science. Researchers have investigated its use as a precursor for synthesizing advanced materials such as conductive polymers and metal-organic frameworks (MOFs). These materials exhibit exceptional properties, including high conductivity and surface area, making them ideal for applications in energy storage and sensor technology.

In conclusion, (2-methylprop-2-en-1-ylium thiourea) continues to be a subject of intense research due to its diverse applications and unique chemical properties. As new studies emerge, this compound is poised to play an even more significant role in advancing various scientific disciplines. Its versatility and adaptability make it a cornerstone for future innovations in chemistry and beyond.

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