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4-Bromobenzaldehyde (CAS 1122-91-4)

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Alternate Names:
p-Bromobenzaldehyde
Application:
4-Bromobenzaldehyde is a compound employed in palladium-catalyzed mono- and bis-arylation of 3,4-(ethylenedioxy)thiophenes
CAS Number:
1122-91-4
Purity:
≥95%
Molecular Weight:
185.02
Molecular Formula:
C7H5BrO
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-Bromobenzaldehyde, an aromatic aldehyde, serves as a versatile chemical compound with various applications. It is widely employed as a reagent in synthesizing a diverse array of organic compounds, including pharmaceuticals, precursor polymers, and dyes. Additionally, it functions as a catalyst in the synthesis of polyurethanes, polyesters, and polyamides. Moreover, 4-Bromobenzaldehyde has found utility in generating novel materials with potential applications in energy storage, nanotechnology, and electronics. The mechanism of action of 4-Bromobenzaldehyde lies in its reactivity towards other molecules. It can undergo reactions with nucleophiles, such as amines and thiols, leading to the formation of substituted benzaldehydes. Similarly, it can react with electrophiles like alkenes and alkynes, resulting in the formation of substituted benzenes. Furthermore, it exhibits reactivity with aldehydes and ketones, leading to the formation of substituted aldehydes and ketones.


4-Bromobenzaldehyde (CAS 1122-91-4) References

  1. Parallel solid-phase synthesis of disubstituted (5-biphenyltetrazolyl) hydantoins and thiohydantoins targeting the growth hormone secretagogue receptor.  |  Severinsen, R., et al. 2004. Bioorg Med Chem Lett. 14: 317-20. PMID: 14698149
  2. A fluorine scan at the catalytic center of thrombin: C--F, C--OH, and C--OMe bioisosterism and fluorine effects on pKa and log D values.  |  Schweizer, E., et al. 2006. ChemMedChem. 1: 611-21. PMID: 16892401
  3. Stereoselective synthesis of (2S,3R)- and (2R,3S)-iodoreboxetine; potential SPECT imaging agents for the noradrenaline transporter.  |  Jobson, NK., et al. 2008. Org Biomol Chem. 6: 2369-76. PMID: 18563271
  4. Synthesis of a polymerizable fluorosurfactant for the construction of stable nanostructured proton-conducting membranes.  |  Wadekar, MN., et al. 2010. J Org Chem. 75: 6814-9. PMID: 20845981
  5. Synthesis, spectroscopic studies, antimicrobial activities and antitumor of a new monodentate V-shaped Schiff base and its transition metal complexes.  |  Ramadan, RM., et al. 2014. Spectrochim Acta A Mol Biomol Spectrosc. 132: 417-22. PMID: 24887503
  6. Optical properties of 4-bromobenzaldehyde derivatives in chloroform solution.  |  Climent, C., et al. 2014. J Phys Chem A. 118: 6914-21. PMID: 25111268
  7. Synthesis of some new carbonitriles and pyrazole coumarin derivatives with potent antitumor and antimicrobial activities.  |  Hafez, OM., et al. 2014. Acta Pol Pharm. 71: 594-601. PMID: 25272885
  8. Theoretical study on catalyzed selective photoreduction mechanism for 4-bromobenzaldehyde in two different solvents.  |  Huang, X., et al. 2015. Phys Chem Chem Phys. 17: 19997-20005. PMID: 26171730
  9. Synthesis, Characterization, Electrical Conductivity and Fluorescence Properties of Polyimine Bearing Phenylacetylene Units.  |  Şenol, D., et al. 2016. J Fluoresc. 26: 1579-90. PMID: 27338948
  10. Semicarbazone EGA Inhibits Uptake of Diphtheria Toxin into Human Cells and Protects Cells from Intoxication.  |  Schnell, L., et al. 2016. Toxins (Basel). 8: PMID: 27428999
  11. Evaluation of aromatic radiobromination by nucleophilic substitution using diaryliodonium salt precursors.  |  Zhou, D., et al. 2017. J Labelled Comp Radiopharm. 60: 450-456. PMID: 28512784
  12. A DFT study on the mechanism of photoselective catalytic reduction of 4-bromobenzaldehyde in different solvents employing an OH-defected TiO2 cluster model.  |  Gan, H., et al. 2017. Phys Chem Chem Phys. 19: 27755-27764. PMID: 28990027
  13. In Vitro and In Vivo Anti-Breast Cancer Activities of Some Synthesized Pyrazolinyl-estran-17-one Candidates.  |  Amr, AEE., et al. 2018. Molecules. 23: PMID: 29958453
  14. Tyrosinase Inhibition by 4-Substituted Benzaldehydes with Electron-Withdrawing Groups.  |  Nihei, KI. and Kubo, I. 2020. Appl Biochem Biotechnol. 191: 1711-1716. PMID: 32212107
  15. Anticonvulsant activities of 4-bromobenzaldehyde semicarbazone.  |  Dimmock, JR. and Baker, GB. 1994. Epilepsia. 35: 648-55. PMID: 8026412

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Bromobenzaldehyde, 10 g

sc-256721
10 g
$38.00

4-Bromobenzaldehyde, 25 g

sc-256721A
25 g
$61.00