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Dibenzothiophene, 98%, Thermo Scientific Chemicals
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Catalog number A12288.22
also known as A12288-22
Price (USD)/ Each
143.65
Online exclusive
159.00 Save 15.35 (10%)
-
Quantity:
100 g
Price (USD)/ Each
143.65
Online exclusive
159.00 Save 15.35 (10%)
Dibenzothiophene, 98%, Thermo Scientific Chemicals
Catalog numberA12288.22
Price (USD)/ Each
143.65
Online exclusive
159.00 Save 15.35 (10%)
-
Chemical Identifiers
CAS132-65-0
IUPAC Name8-thiatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene
Molecular FormulaC12H8S
InChI KeyIYYZUPMFVPLQIF-UHFFFAOYSA-N
SMILESS1C2=C(C=CC=C2)C2=C1C=CC=C2
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Specifications
Specification Sheet
Specification SheetFormPowder
Appearance (Color)White to pale cream or pale yellow
Identification (FTIR)Conforms
Solution Test5% in acetone; clear to slightly hazy yellow solution
Assay (GC)≥97.5%
Dibenzothiophene is used to investigate the effect of sulfur compounds in gasoline range during the fluid catalytic cracking (FCC) process.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Dibenzothiophene is used to investigate the effect of sulfur compounds in gasoline range during the fluid catalytic cracking (FCC) process.
Solubility
Soluble in water.
Notes
Incompatible with strong oxidizing agents.
Dibenzothiophene is used to investigate the effect of sulfur compounds in gasoline range during the fluid catalytic cracking (FCC) process.
Solubility
Soluble in water.
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Lithiation occurs at the 4-position (ortho to the S atom). The lithio-derivative reacts with electrophiles, such as bromine: J. Am. Chem. Soc., 76, 5786 (1954).
- Trehoux, A.; Roux, Y.; Guillot, R.; Mahy, J. P.; Avenier, F. Catalytic oxidation of dibenzothiophene and thioanisole by a diiron(III) complex and hydrogen peroxide. J. Mol. Catal. A: Chem. 2015, 396, 40-46.
- Fan, C.; Duan, C.; Wei, Y.; Ding, D.; Xu, H.; Huang, W. Dibenzothiophene-Based Phosphine Oxide Host and Electron-Transporting Materials for Efficient Blue Thermally Activated Delayed Fluorescence Diodes through Compatibility Optimization. Chem. Mater. 2015, 27 (14), 5131-5140.