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Dibenzothiophene 5-oxide (CAS 1013-23-6)

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Alternate Names:
Dibenzothiophene S-oxide
Application:
CAS Number:
1013-23-6
Molecular Weight:
200.26
Molecular Formula:
C12H8OS
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Dibenzothiophene 5-oxide is a chemical compound that functions as an oxidizing agent in various experimental applications. It acts by participating in redox reactions, transferring oxygen atoms to other molecules, thereby facilitating the oxidation of organic substrates. Dibenzothiophene 5-Oxide′s mechanism of action involves the formation of reactive oxygen species, which can then react with target molecules, leading to the modification of their chemical structure. In this way, dibenzothiophene 5-oxide may play a role in the oxidation of organic compounds, contributing to the synthesis of specific chemical products or the modification of molecular structures in research and development applications. Its ability to facilitate oxidation reactions may be a useful for experimental purposes, where the modification of organic substrates is required for the synthesis of new compounds or the study of specific chemical reactions.


Dibenzothiophene 5-oxide (CAS 1013-23-6) References

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  2. Synthesis of glycosyl-1-phosphates via dehydrative glycosylation.  |  Garcia, BA. and Gin, DY. 2000. Org Lett. 2: 2135-8. PMID: 10891249
  3. Stereoselective synthesis of 2-hydroxy-alpha-mannopyranosides from glucal donors.  |  Kim, JY., et al. 2001. Org Lett. 3: 303-6. PMID: 11430060
  4. Stepwise Oxidation of Thiophene and Its Derivatives by Hydrogen Peroxide Catalyzed by Methyltrioxorhenium(VII).  |  Brown, KN. and Espenson, JH. 1996. Inorg Chem. 35: 7211-7216. PMID: 11666909
  5. Molecular analysis of arylalcohol dehydrogenase of Coriolus versicolor expressed against exogenous addition of dibenzothiophene derivatives.  |  Ichinose, H., et al. 2002. J Basic Microbiol. 42: 327-36. PMID: 12362404
  6. Elucidation of the metabolic pathway of fluorene and cometabolic pathways of phenanthrene, fluoranthene, anthracene and dibenzothiophene by Sphingomonas sp. LB126.  |  van Herwijnen, R., et al. 2003. Res Microbiol. 154: 199-206. PMID: 12706509
  7. Degradation of polycyclic aromatic hydrocarbons by a newly isolated dibenzofuran-utilizing Janibacter sp. strain YY-1.  |  Yamazoe, A., et al. 2004. Appl Microbiol Biotechnol. 65: 211-8. PMID: 14740192
  8. Photochemistry and photophysics of halogen-substituted dibenzothiophene oxides.  |  Nag, M. and Jenks, WS. 2004. J Org Chem. 69: 8177-82. PMID: 15549784
  9. Desulfurization of dibenzothiophene by Corynebacterium sp. strain SY1.  |  Omori, T., et al. 1992. Appl Environ Microbiol. 58: 911-5. PMID: 1575493
  10. Selective Desulfurization of Dibenzothiophene by Rhodococcus erythropolis D-1.  |  Izumi, Y., et al. 1994. Appl Environ Microbiol. 60: 223-6. PMID: 16349153
  11. Characterization of new oxidation products of 9H-carbazole and structure related compounds by biphenyl-utilizing bacteria.  |  Waldau, D., et al. 2009. Appl Microbiol Biotechnol. 81: 1023-31. PMID: 18836714
  12. Isolation and classification of a soil actinomycete capable of sulphur-specific biotransformation of dibenzothiophene, benzothiophene and thianthrene.  |  Khedkar, S. and Shanker, R. 2015. J Appl Microbiol. 118: 62-74. PMID: 25319398
  13. Metabolism of dibenzothiophene by a Beijerinckia species.  |  Laborde, AL. and Gibson, DT. 1977. Appl Environ Microbiol. 34: 783-90. PMID: 596875
  14. Elucidation of the metabolic pathway for dibenzothiophene desulphurization by Rhodococcus sp. strain IGTS8 (ATCC 53968).  |  Oldfield, C., et al. 1997. Microbiology (Reading). 143 (Pt 9): 2961-2973. PMID: 9308179
  15. Biodegradation of dibenzothiophene by a nodulating isolate of Rhizobium meliloti.  |  Frassinetti, S., et al. 1998. Can J Microbiol. 44: 289-97. PMID: 9606911

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Dibenzothiophene 5-oxide, 100 mg

sc-263088
100 mg
$92.00

Dibenzothiophene 5-oxide, 1 g

sc-263088A
1 g
$450.00