Date published: 2025-12-15

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4-Allyloxybenzaldehyde (CAS 40663-68-1)

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CAS Number:
40663-68-1
Purity:
97%
Molecular Weight:
162.19
Molecular Formula:
C10H10O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4-Allyloxybenzaldehyde is a chemical compound that functions as a versatile building block in organic synthesis. Its mode of action involves participating in various reactions such as the Claisen-Schmidt condensation, Michael addition, and Wittig reaction. In these processes, 4-Allyloxybenzaldehyde serves as a key intermediate for the synthesis of complex organic molecules, allowing for the introduction of the allyloxy group into the target compounds. 4-Allyloxybenzaldehyde′s functional role lies in its ability to undergo these reactions, leading to the formation of new carbon-carbon and carbon-oxygen bonds. Through its mode of action, 4-Allyloxybenzaldehyde contributes to the development of diverse organic compounds with potential applications in materials science, and agrochemicals.


4-Allyloxybenzaldehyde (CAS 40663-68-1) References

  1. (3E,5E)-3,5-Bis(4-allyl-oxybenzyl-idene)-1-benzyl-piperidin-4-one.  |  Karthikeyan, NS., et al. 2009. Acta Crystallogr Sect E Struct Rep Online. 65: o3062. PMID: 21578792
  2. Design, synthesis, and characterization of novel apigenin analogues that suppress pancreatic stellate cell proliferation in vitro and associated pancreatic fibrosis in vivo.  |  Chen, H., et al. 2014. Bioorg Med Chem. 22: 3393-404. PMID: 24837156
  3. GaN nanowires as a reusable photoredox catalyst for radical coupling of carbonyl under blacklight irradiation.  |  Liu, M., et al. 2020. Chem Sci. 11: 7864-7870. PMID: 34123073
  4. Exploring the Monoterpene Indole Alkaloid Scaffold for Reversing P-Glycoprotein-Mediated Multidrug Resistance in Cancer.  |  Cardoso, DSP., et al. 2021. Pharmaceuticals (Basel). 14: PMID: 34577562
  5. Synthesis and Application of Trehalose Materials.  |  Vinciguerra, D., et al. 2022. JACS Au. 2: 1561-1587. PMID: 35911465
  6. Peripheral Groups of Dicationic Pyrazinoporphyrins Regulate Lipid Membrane Binding.  |  Polivanovskaia, DA., et al. 2022. Membranes (Basel). 12: PMID: 36135866

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Allyloxybenzaldehyde, 10 g

sc-232375
10 g
$52.00