Date published: 2025-10-2

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N-Allylurea (CAS 557-11-9)

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Alternate Names:
1-Prop-2-en-1-ylurea
CAS Number:
557-11-9
Purity:
95%
Molecular Weight:
100.12
Molecular Formula:
C4H8N2O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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N-Allylurea is a compound that functions as a precursor in the synthesis of various organic compounds. It acts as a reactant in the production of polymers and agrochemicals. Its mechanism of action involves participating in chemical reactions as a starting material, leading to the formation of new chemical entities. N-Allylurea undergoes specific transformations, such as nucleophilic addition and substitution, to yield products with diverse applications in research and development. Its reactivity and ability to form covalent bonds make it a versatile building block for the creation of complex molecules with potential utility in various scientific fields. N-Allylurea′s role in chemical synthesis contributes to the advancement of knowledge and innovation in the development of novel materials and compounds.


N-Allylurea (CAS 557-11-9) References

  1. Physical stabilization of starch-allylurea blends by EB-grafting: a compositional and structural study.  |  Olivier, A., et al. 2000. Biomacromolecules. 1: 282-9. PMID: 11710112
  2. Compatibilization of starch-allylurea blends by electron beam irradiation: spectroscopic monitoring and assessment of grafting efficiency.  |  Olivier, A., et al. 2001. Biomacromolecules. 2: 1260-6. PMID: 11777401
  3. Identification of 1-arylmethyl-3- (2-aminoethyl)-5-aryluracil as novel gonadotropin-releasing hormone receptor antagonists.  |  Zhu, YF., et al. 2003. J Med Chem. 46: 2023-6. PMID: 12747774
  4. Synthesis and structure-activity relationships of 1-arylmethyl-5-aryl-6-methyluracils as potent gonadotropin-releasing hormone receptor antagonists.  |  Guo, Z., et al. 2004. J Med Chem. 47: 1259-71. PMID: 14971906
  5. Palladium-Catalyzed Carboetherification and Carboamination Reactions of γ-Hydroxy- and γ-Aminoalkenes for the Synthesis of Tetrahydrofurans and Pyrrolidines.  |  Wolfe, JP. 2007. European J Org Chem. 2007: 571-582. PMID: 20577649
  6. Synergistically Enhanced Polysulfide Chemisorption Using a Flexible Hybrid Separator with N and S Dual-Doped Mesoporous Carbon Coating for Advanced Lithium-Sulfur Batteries.  |  Balach, J., et al. 2016. ACS Appl Mater Interfaces. 8: 14586-95. PMID: 27225061

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

N-Allylurea, 25 g

sc-235990
25 g
$41.00