Date published: 2025-12-16

1-800-457-3801

SCBT Portrait Logo
Seach Input

2,6-Dibromoquinone-4-chloroimide (CAS 537-45-1)

5.0(1)
Write a reviewAsk a question

Alternate Names:
2,6-Dibromo-N-chloro-p-benzoquinoneimine
Application:
2,6-Dibromoquinone-4-chloroimide is a phenol detecting reagent
CAS Number:
537-45-1
Purity:
≥96%
Molecular Weight:
299.35
Molecular Formula:
C6H2Br2ClNO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

2,6-Dibromoquinone-4-chloroimide is a reagent for the determination of phenols. The compound, 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone, plays a significant role in scientific research, particularly in organic synthesis. It facilitates the synthesis of various compounds and also acts as a reagent in biochemical and physiological studies. Its versatile nature enables it to aid in the detection of proteins, nucleic acids, and other biomolecules. Due to its high reactivity, 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone readily forms covalent bonds with a wide range of molecules. This property allows it to react with proteins, nucleic acids, and other biomolecules, leading to the formation of covalent bonds.


2,6-Dibromoquinone-4-chloroimide (CAS 537-45-1) References

  1. THE BACTERIAL DEGRADATION OF CATECHOL.  |  DAGLEY, S. and GIBSON, DT. 1965. Biochem J. 95: 466-74. PMID: 14340096
  2. Response of enzyme activities and microbial communities to soil amendment with sugar alcohols.  |  Yu, H., et al. 2016. Microbiologyopen. 5: 604-15. PMID: 27005019
  3. Novel Organophosphate Ligand O-(2-Fluoroethyl)-O-(p-Nitrophenyl)Methylphosphonate: Synthesis, Hydrolytic Stability and Analysis of the Inhibition and Reactivation of Cholinesterases.  |  Chao, CK., et al. 2016. Chem Res Toxicol. 29: 1810-1817. PMID: 27551891
  4. An improved radiosynthesis of O-(2-[18 F]fluoroethyl)-O-(p-nitrophenyl)methylphosphonate: A first-in-class cholinesterase PET tracer.  |  Neumann, KD., et al. 2017. J Labelled Comp Radiopharm. 60: 337-342. PMID: 28406525
  5. Combined use of a microbial restoration substrate and avirulent Ralstonia solanacearum for the control of tomato bacterial wilt.  |  Zheng, X., et al. 2019. Sci Rep. 9: 20091. PMID: 31882824
  6. Increasing the Efficacy of Seproxetine as an Antidepressant Using Charge-Transfer Complexes.  |  Alsanie, WF., et al. 2022. Molecules. 27: PMID: 35630766
  7. Attempting to Increase the Effectiveness of the Antidepressant Trazodone Hydrochloride Drug Using π-Acceptors.  |  Alsanie, WF., et al. 2022. Int J Environ Res Public Health. 19: PMID: 36141553
  8. Multispectral and Molecular Docking Studies Reveal Potential Effectiveness of Antidepressant Fluoxetine by Forming π-Acceptor Complexes.  |  Gaber, A., et al. 2022. Molecules. 27: PMID: 36144618
  9. Evaluation of exposure to phenol: absorption of phenol vapour in the lungs and through the skin and excretion of phenol in urine.  |  Piotrowski, JK. 1971. Br J Ind Med. 28: 172-8. PMID: 5572685
  10. Catabolism of phenylpropionic acid and its 3-hydroxy derivative by Escherichia coli.  |  Burlingame, R. and Chapman, PJ. 1983. J Bacteriol. 155: 113-21. PMID: 6345502
  11. Catabolism of pseudocumene and 3-ethyltoluene by Pseudomonas putida (arvilla) mt-2: evidence for new functions of the TOL (pWWO) plasmid.  |  Kunz, DA. and Chapman, PJ. 1981. J Bacteriol. 146: 179-91. PMID: 7216999
  12. Bacterial degradation of 3,4,5-trimethoxyphenylacetic and 3-ketoglutaric acids.  |  Donnelly, MI., et al. 1981. J Bacteriol. 147: 477-81. PMID: 7263613
  13. Production of methanol from aromatic acids by Pseudomonas putida.  |  Donnelly, MI. and Dagley, S. 1980. J Bacteriol. 142: 916-24. PMID: 7380811

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,6-Dibromoquinone-4-chloroimide, 5 g

sc-358745
5 g
$189.00