Cas no 108009-46-7 (1,3-Diphenyl-d10-urea)

1,3-Diphenyl-d10-urea is a deuterated analog of 1,3-diphenylurea, where ten hydrogen atoms are replaced with deuterium. This isotopic labeling enhances the compound's utility in NMR spectroscopy and mass spectrometry, providing improved signal resolution and reduced background interference. Its high isotopic purity makes it valuable for mechanistic studies, metabolic tracing, and kinetic isotope effect investigations. The compound retains the chemical properties of its non-deuterated counterpart while offering distinct advantages in research applications requiring precise molecular tracking. Suitable for use in pharmaceutical and chemical research, 1,3-Diphenyl-d10-urea serves as a reliable standard or reagent in deuterium-labeled synthetic pathways and analytical methodologies.
1,3-Diphenyl-d10-urea structure
1,3-Diphenyl-d10-urea structure
Product Name:1,3-Diphenyl-d10-urea
CAS No:108009-46-7
MF:C13H12N2O
MW:222.308799743652
CID:892024
Update Time:2025-11-01

1,3-Diphenyl-d10-urea Chemical and Physical Properties

Names and Identifiers

    • Urea, N,N'-di(phenyl-d5)-
    • 1,3-Diphenyl-d10-urea
    • N,N′-DIPHENYLUREA D10
    • proximpham d10
    • 1,3-bis(2,3,4,5,6-pentadeuteriophenyl)urea
    • Inchi: 1S/C13H12N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10H,(H2,14,15,16)/i1D,2D,3D,4D,5D,6D,7D,8D,9D,10D
    • InChI Key: GWEHVDNNLFDJLR-LHNTUAQVSA-N
    • SMILES: C1(NC(=O)NC2=C([2H])C([2H])=C([2H])C([2H])=C2[2H])=C([2H])C(=C([2H])C([2H])=C1[2H])[2H]

Computed Properties

  • Exact Mass: 222.15800

Experimental Properties

  • PSA: 41.13000
  • LogP: 3.47660

1,3-Diphenyl-d10-urea Pricemore >>

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Additional information on 1,3-Diphenyl-d10-urea

Introduction to 1,3-Diphenyl-d10-urea (CAS No. 108009-46-7) and Its Emerging Applications in Chemical Biology

The compound 1,3-Diphenyl-d10-urea (CAS No. 108009-46-7) represents a fascinating molecule in the realm of chemical biology, characterized by its unique structural and functional properties. As a deuterated derivative of 1,3-diphenylurea, this compound has garnered significant attention due to its potential applications in pharmaceutical research, agrochemical development, and material science. The introduction of deuterium atoms (denoted by the suffix "-d10") not only modifies its physical and chemical properties but also enhances its stability and metabolic resistance, making it an attractive candidate for various scientific investigations.

In recent years, the field of drug discovery has witnessed a surge in the use of deuterated compounds to improve drug efficacy and reduce side effects. The incorporation of deuterium atoms into molecular structures can alter metabolic pathways, leading to increased bioavailability and prolonged half-life. This concept, known as "deuterium effect," has been extensively studied in the development of antiviral, anticancer, and anti-inflammatory agents. The 1,3-Diphenyl-d10-urea molecule exemplifies this trend, as its deuterated form exhibits enhanced binding affinity to certain biological targets while maintaining structural integrity.

One of the most compelling aspects of 1,3-Diphenyl-d10-urea is its versatility in chemical synthesis. The presence of two phenyl rings and a urea functional group provides multiple sites for functionalization, enabling researchers to design derivatives with tailored properties. For instance, this compound can serve as a key intermediate in the synthesis of complex organic molecules, including those with pharmaceutical relevance. Its stability under various reaction conditions makes it a preferred choice for multi-step synthetic routes, where high yields and minimal degradation are critical.

The structural motif of 1,3-Diphenylurea (and its deuterated variant) has been explored in several cutting-edge research areas. In particular, its ability to interact with biological macromolecules has opened new avenues in medicinal chemistry. Researchers have leveraged this compound to develop inhibitors targeting enzymes involved in metabolic diseases and cancer progression. The deuterated version further enhances these interactions by reducing enzymatic degradation, thereby improving therapeutic outcomes. For example, studies have shown that derivatives of 1,3-Diphenyl-d10-urea exhibit potent inhibitory effects on kinases and proteases implicated in tumor growth and metastasis.

Moreover, the agrochemical sector has recognized the potential of 1,3-Diphenyl-d10-urea as a precursor for novel pesticides and herbicides. Its phenyl rings contribute to lipophilicity and membrane permeability, essential traits for effective pest control agents. Recent advancements in green chemistry have prompted researchers to explore sustainable synthetic routes for this compound, emphasizing atom economy and minimal waste generation. Such efforts align with global initiatives to develop environmentally friendly agrochemicals without compromising efficacy.

The material science applications of 1,3-Diphenyl-d10-urea are equally noteworthy. Its unique electronic properties make it suitable for use in organic semiconductors and light-emitting diodes (OLEDs). The deuterated version enhances thermal stability, allowing for more durable electronic devices. This has sparked interest among industry researchers who are seeking materials that can withstand harsh operating conditions while maintaining performance efficiency.

In conclusion,1,3-Diphenyl-d10-urea (CAS No. 108009-46-7) stands as a versatile compound with far-reaching implications across multiple scientific disciplines. Its structural features and deuterium-labeled variant offer distinct advantages in pharmaceutical design, agrochemical innovation, and advanced materials development. As research continues to uncover new applications for this molecule,1,3-Diphenyl-d10-urea is poised to play a pivotal role in shaping the future of chemical biology and related fields.

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