Date published: 2026-2-7

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4-Acetamidobenzaldehyde (CAS 122-85-0)

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Alternate Names:
4′-Formylacetanilide
CAS Number:
122-85-0
Molecular Weight:
163.17
Molecular Formula:
C9H9NO2
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-Acetamidobenzaldehyde is a chemical compound that functions as a key intermediate in organic synthesis. Its mode of action involves participating in various reactions to form complex organic molecules. It can undergo condensation reactions to form imines, which are important intermediates in the synthesis of agrochemicals, and other fine chemicals. 4-Acetamidobenzaldehyde can serve as a building block for the preparation of heterocyclic compounds, which are medicinal chemistry and material science. Its functional role lies in its ability to facilitate the creation of diverse chemical structures, making it a versatile for the development of new compounds with potential applications in various fields of development.


4-Acetamidobenzaldehyde (CAS 122-85-0) References

  1. Microwave-assisted, one-pot reaction of 7-azaindoles and aldehydes: a facile route to novel di-7-azaindolylmethanes.  |  Uddin, MI., et al. 2014. Tetrahedron Lett. 55: PMID: 24396154
  2. Synthesis and evaluation of new fluorinated anti-tubercular compounds.  |  Esfahanizadeh, M., et al. 2014. Iran J Pharm Res. 13: 115-26. PMID: 24734062
  3. Highly Efficient Cell Membrane Tracker Based on a Solvatochromic Dye with Near-Infrared Emission.  |  Liu, H., et al. 2020. ACS Omega. 5: 11829-11835. PMID: 32478274
  4. An atom-economical addition of methyl azaarenes with aromatic aldehydes via benzylic C(sp3)-H bond functionalization under solvent- and catalyst-free conditions.  |  Yennamaneni, DR., et al. 2020. Beilstein J Org Chem. 16: 3093-3103. PMID: 33425033
  5. Photophysical and Bactericidal Properties of Pyridinium and Imidazolium Porphyrins for Photodynamic Antimicrobial Chemotherapy.  |  Le Guern, F., et al. 2021. Molecules. 26: PMID: 33672630
  6. Synthesis and biological evaluations of oleanolic acid indole derivatives as hyaluronidase inhibitors with enhanced skin permeability.  |  He, H., et al. 2021. J Enzyme Inhib Med Chem. 36: 1665-1678. PMID: 34309457
  7. Glyconanoparticles with Activatable Near-Infrared Probes for Tumor-Cell Imaging and Targeted Drug Delivery.  |  Chi, G., et al. 2022. Int J Nanomedicine. 17: 1567-1575. PMID: 35401000
  8. An aerobic oxidation of alcohols into carbonyl synthons using bipyridyl-cinchona based palladium catalyst.  |  Cheedarala, RK., et al. 2021. RSC Adv. 11: 32942-32954. PMID: 35493605
  9. Privileged Scaffold Decoration for the Identification of the First Trisubstituted Triazine with Anti-SARS-CoV-2 Activity.  |  Cesarini, S., et al. 2022. Molecules. 27: PMID: 36557962
  10. Design, Synthesis, and In Vitro and In Silico Approaches of Novel Indanone Derivatives as Multifunctional Anti-Alzheimer Agents.  |  Sağlık, BN., et al. 2022. ACS Omega. 7: 47378-47404. PMID: 36570177
  11. Thioacetalation and Multi-Component Thiomethylative Friedel-Crafts Arylation Using BF3SMe2.  |  Söderström, M., et al. 2023. ACS Omega. 8: 4320-4330. PMID: 36743056
  12. A genome-wide CRISPR-Cas9 knockout screen identifies FSP1 as the warfarin-resistant vitamin K reductase.  |  Jin, DY., et al. 2023. Nat Commun. 14: 828. PMID: 36788244
  13. Synthesis and Biological Properties of EGFR-Targeted Photosensitizer Based on Cationic Porphyrin.  |  Bortnevskaya, YS., et al. 2023. Pharmaceutics. 15: PMID: 37111769

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Acetamidobenzaldehyde, 5 g

sc-232359
5 g
$37.00