Molecular structure of 2,3-Dibromo-1,4-naphthoquinone, CAS Number: 13243-65-7
2,3-Dibromo-1,4-naphthoquinone (CAS 13243-65-7)
CAS Number:
13243-65-7
Molecular Weight:
315.95
Molecular Formula:
C10H4Br2O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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2,3-Dibromo-1,4-naphthoquinone (2,3-DBNQ) is a significant organic compound widely employed as an intermediate in the synthesis of various products. With a 1,4-naphthoquinone ring bearing two bromine atoms, it is classified as a conjugated diene. The precise mechanism of action of 2,3-Dibromo-1,4-naphthoquinone remains incompletely understood. However, it is believed to function as an inhibitor of the enzyme squalene epoxidase, which plays a role in the biosynthesis of ergosterol—an essential component of fungal cell membranes.
2,3-Dibromo-1,4-naphthoquinone (CAS 13243-65-7) References
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- Cytotoxicity of naphthoquinones and their capacity to generate reactive oxygen species is quenched when conjugated with gold nanoparticles. | Srinivas, P., et al. 2011. Int J Nanomedicine. 6: 2113-22. PMID: 22114475
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- Time-resolved visible and infrared absorption spectroscopy data obtained using photosystem I particles with non-native quinones incorporated into the A1 binding site. | Makita, H. and Hastings, G. 2016. Data Brief. 7: 1463-8. PMID: 27182540
- Development of a Bioluminescent High-Throughput Screening Assay for Nicotinamide Mononucleotide Adenylyltransferase (NMNAT). | Haubrich, BA., et al. 2020. SLAS Discov. 25: 33-42. PMID: 31583955
- Time-resolved FTIR difference spectroscopy for the study of photosystem I with high potential naphthoquinones incorporated into the A1 binding site. | Agarwala, N., et al. 2023. Biochim Biophys Acta Bioenerg. 1864: 148918. PMID: 36116485
- Dyes derived from 1, 4‐naphthoquinone as initiators for radical and cationic photopolymerisation | Szymczak, A. M., Podsiadły, R., Podemska, K., & Sokołowska, J. 2012. Coloration Technology. 128(5): 378-386.
- Synthesis, characterization and molecular structures of homologated analogs of 2-bromo-3-(n-alkylamino)-1, 4-napthoquinone | Salunke-Gawali, S., Pawar, O., Nikalje, M., Patil, R., Weyhermüller, T., Puranik, V. G., & Konkimalla, V. B. 2014. Journal of Molecular Structure. 1056: 97-103.
- Synthesis, Electrochemistry, DFT Calculations, Antimicrobial Properties and X‐ray Crystal Structures of Some NH‐and/or S‐Substituted‐1, 4‐quinones | Kacmaz, A., Acar, E. T., Atun, G., Kaya, K., Sigirci, B. D., & Bagcigil, F. 2018. Chemistryselect. 3(30): 8615-8623.
- New NH-substituted 1, 4-naphtho-and 1, 4-benzo-quinones: Synthesis, characterization and potential antiproliferative effect against MDA-MB-231 cells | Kacmaz, A., & Hamurcu, Z. 2018. Phosphorus, Sulfur, and Silicon and the Related Elements. 193(12): 831-839.
- Synthesis of ferrocene based naphthoquinones and its application as novel non‐enzymatic hydrogen peroxide | Ertas, N. A., Kavak, E., Salman, F., Kazici, H. C., Kivrak, H., & Kivrak, A. 2020. Electroanalysis. 32(6): 1178-1185.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2,3-Dibromo-1,4-naphthoquinone, 25 g | sc-225591 | 25 g | $242.00 |