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3-Vinylbenzaldehyde (CAS 19955-99-8)

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CAS Number:
19955-99-8
Purity:
97%
Molecular Weight:
132.16
Molecular Formula:
C9H8O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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3-Vinylbenzaldehyde (3-VBA) is a colorless liquid with a pleasant odor and a boiling point of 118-119°C. It holds significant importance as an organic compound extensively utilized in synthesizing a wide range of organic compounds. Its versatility and usefulness as a building block for organic synthesis make it a valuable component in various applications, including medicine and agrochemicals. This compound has proven its worth in scientific research, enabling the synthesis of diverse organic compounds, investigating the mechanism of drug action, and studying the biochemical and physiological effects of drugs. As a pivotal intermediate in the synthesis of multiple organic compounds, 3-Vinylbenzaldehyde plays a role in the creation of drugs and agrochemicals.


3-Vinylbenzaldehyde (CAS 19955-99-8) References

  1. Polymerization-Induced Self-Assembly (PISA) - Control over the Morphology of 19F-Containing Polymeric Nano-objects for Cell Uptake and Tracking.  |  Zhao, W., et al. 2017. Biomacromolecules. 18: 1145-1156. PMID: 28339189
  2. Identification and functional characterization of an odorant receptor in pea aphid, Acyrthosiphon pisum.  |  Zhang, RB., et al. 2019. Insect Sci. 26: 58-67. PMID: 28730637
  3. Delivery of Amonafide from Fructose-Coated Nanodiamonds by Oxime Ligation for the Treatment of Human Breast Cancer.  |  Zhao, J., et al. 2018. Biomacromolecules. 19: 481-489. PMID: 29316394
  4. Use of Core-Cross-Linked Polymeric Micelles Induced by the Selective Detection of Cu(II) Ions for the Sustained Release of a Model Drug.  |  Bak, JM. and Lee, HI. 2019. ACS Appl Mater Interfaces. 11: 14368-14375. PMID: 30916935
  5. Identification of Semiochemicals from Cowpea, Vigna unguiculata, for Low-input Management of the Legume Pod Borer, Maruca vitrata.  |  Osei-Owusu, J., et al. 2020. J Chem Ecol. 46: 288-298. PMID: 31953705
  6. Polymeric Nitrons. 2. Synthesis, Irradiation and Waveguide Mode Spectroscopy of Polymeric Nitrons Derived from Polymeric Benzaldehydes and N-Isopropylhydroxylamine  |  Heinenberg, M., Menges, B., Mittler, S., & Ritter, H. 2002. Macromolecules. 35(9): 3448-3455.
  7. A novel de-cross-linking system from cross-linked polymer to linear polymer utilizing pressure or visible light irradiation  |  Iwamura, T., & Sakaguchi, M. 2008. Macromolecules. 41(23): 8995-8999.
  8. Multienzymatic preparation of (−)-[3-(oxiran-2-yl) phenyl] methanol and (−)-3-(oxiran-2-yl) benzoic acid  |  Sello, G., Bernasconi, S., Orsini, F., & Di Gennaro, P. 2009. Tetrahedron: Asymmetry. 20(5): 563-565.
  9. New benzylidene oxazolone derived polymeric photoswitches for light-induced tunable thermoresponsive behaviors  |  Balamurugan, A., & Lee, H. I. 2014. Polymer Chemistry. 5(22): 6426-6430.
  10. Chirped-pulse microwave spectrum and ab initio calculations of four distinct conformers of 3-vinylbenzaldehyde  |  Smith, M., Short, B. D., Ruthven, A. M., Thomas, K. M., Hang, M. J., & Brown, G. G. 2015. Journal of Molecular Spectroscopy. 307: 49-53.
  11. Water-soluble polymeric probe for the selective sensing and separation of Cu (II) ions in aqueous media: pH-tunable detection sensitivity and efficient separation by thermal precipitation  |  Bak, J. M., & Lee, H. I. 2017. Macromolecules. 50(21): 8529-8535.
  12. Water-soluble polymeric probe with dual recognition sites for the sequential colorimetric detection of cyanide and Fe (III) ions  |  Gupta, M., & Lee, H. I. 2019. Dyes and Pigments. 167: 174-180.
  13. Efficient colorimetric detection of cyanide ions using hemicyanine-based polymeric probes with detection-induced self-assembly in water  |  Bak, J. M., Gupta, M., Jung, S. H., & Lee, H. I. 2021. Polymer. 213: 123320.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3-Vinylbenzaldehyde, 5 g

sc-226190
5 g
$317.00