Cas no 1038374-89-8 (3-(Dimethylamino)-2,2-dimethylpropylthiourea)

3-(Dimethylamino)-2,2-dimethylpropylthiourea is a thiourea derivative characterized by its tertiary amine and sterically hindered alkyl groups. This structural configuration enhances its stability and reactivity, making it suitable for applications in organic synthesis and coordination chemistry. The compound’s thiourea moiety allows for strong ligand properties, facilitating metal ion chelation and catalysis. Its dimethylamino group contributes to solubility in polar solvents, while the branched alkyl chain improves steric control in reaction pathways. This combination of features makes it a valuable intermediate for specialized chemical processes, particularly where selective binding or controlled reactivity is required. Its well-defined structure ensures consistent performance in synthetic applications.
3-(Dimethylamino)-2,2-dimethylpropylthiourea structure
1038374-89-8 structure
Product Name:3-(Dimethylamino)-2,2-dimethylpropylthiourea
CAS No:1038374-89-8
MF:C8H19N3S
MW:189.321560144424
CID:5055738
Update Time:2025-11-02

3-(Dimethylamino)-2,2-dimethylpropylthiourea Chemical and Physical Properties

Names and Identifiers

    • [3-(dimethylamino)-2,2-dimethylpropyl]thiourea
    • NE37293
    • 3-(Dimethylamino)-2,2-dimethylpropylthiourea
    • Inchi: 1S/C8H19N3S/c1-8(2,6-11(3)4)5-10-7(9)12/h5-6H2,1-4H3,(H3,9,10,12)
    • InChI Key: GJYPZDJSYRBASI-UHFFFAOYSA-N
    • SMILES: S=C(N)NCC(C)(C)CN(C)C

Computed Properties

  • Exact Mass: 189.13
  • Monoisotopic Mass: 189.13
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 4
  • Complexity: 154
  • 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: 0.8
  • Topological Polar Surface Area: 73.4

3-(Dimethylamino)-2,2-dimethylpropylthiourea Pricemore >>

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Additional information on 3-(Dimethylamino)-2,2-dimethylpropylthiourea

Comprehensive Guide to 3-(Dimethylamino)-2,2-dimethylpropylthiourea (CAS No. 1038374-89-8): Properties, Applications, and Market Insights

3-(Dimethylamino)-2,2-dimethylpropylthiourea (CAS No. 1038374-89-8) is a specialized organic compound that has garnered significant attention in the chemical and pharmaceutical industries. This thiourea derivative is characterized by its unique molecular structure, which includes a dimethylamino group and a dimethylpropyl backbone. Its chemical formula and structural features make it a versatile intermediate in synthetic chemistry, particularly in the development of advanced materials and bioactive molecules.

The compound's thiourea moiety is a key functional group that contributes to its reactivity and utility in various chemical reactions. Researchers and industry professionals often explore 3-(Dimethylamino)-2,2-dimethylpropylthiourea for its potential in catalysis, polymer chemistry, and as a building block for more complex molecules. Its CAS No. 1038374-89-8 serves as a unique identifier, ensuring precise communication and documentation in scientific literature and regulatory contexts.

One of the most frequently asked questions about 3-(Dimethylamino)-2,2-dimethylpropylthiourea is its solubility and stability under different conditions. Studies indicate that this compound exhibits moderate solubility in polar organic solvents such as ethanol, acetone, and dimethyl sulfoxide (DMSO). Its stability is generally high under ambient conditions, but it may degrade under extreme pH or prolonged exposure to light. These properties are critical for researchers who need to handle and store the compound effectively.

In recent years, the demand for 3-(Dimethylamino)-2,2-dimethylpropylthiourea has increased due to its applications in the synthesis of pharmaceuticals and agrochemicals. For instance, it has been used as a key intermediate in the production of compounds with potential antibacterial and antifungal properties. The rise of antibiotic-resistant pathogens has spurred interest in novel thiourea derivatives, making CAS No. 1038374-89-8 a compound of interest in drug discovery pipelines.

Another area where 3-(Dimethylamino)-2,2-dimethylpropylthiourea shows promise is in material science. Its ability to act as a ligand or cross-linking agent has been explored in the development of polymers with enhanced mechanical and thermal properties. Researchers are also investigating its role in the synthesis of conductive polymers, which are essential for next-generation electronics and energy storage devices.

The global market for 3-(Dimethylamino)-2,2-dimethylpropylthiourea is influenced by trends in the pharmaceutical and specialty chemicals sectors. With the growing emphasis on sustainable and green chemistry, manufacturers are exploring eco-friendly synthesis routes for this compound. Additionally, regulatory frameworks such as REACH and FDA guidelines impact its production and distribution, ensuring safety and compliance in its use.

For those seeking to purchase 3-(Dimethylamino)-2,2-dimethylpropylthiourea, it is essential to source it from reputable suppliers who provide detailed technical data sheets (TDS) and certificates of analysis (CoA). The compound's purity, typically ranging from 95% to 99%, is a critical factor for its performance in research and industrial applications. Pricing trends indicate that demand for high-purity grades of CAS No. 1038374-89-8 has led to competitive pricing in the global market.

In conclusion, 3-(Dimethylamino)-2,2-dimethylpropylthiourea (CAS No. 1038374-89-8) is a multifaceted compound with significant potential in pharmaceuticals, agrochemicals, and material science. Its unique properties and applications make it a valuable asset for researchers and industry professionals alike. As scientific advancements continue, the role of this thiourea derivative is expected to expand, driving further innovation and market growth.

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