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D32407

Sigma-Aldrich

Dibenzothiophene sulfone

97%

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About This Item

Empirical Formula (Hill Notation):
C12H8O2S
CAS Number:
Molecular Weight:
216.26
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

solid

mp

231-233 °C (lit.)

SMILES string

O=S1(=O)c2ccccc2-c3ccccc13

InChI

1S/C12H8O2S/c13-15(14)11-7-3-1-5-9(11)10-6-2-4-8-12(10)15/h1-8H

InChI key

IKJFYINYNJYDTA-UHFFFAOYSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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S A Denome et al.
Journal of bacteriology, 176(21), 6707-6716 (1994-11-01)
Rhodococcus sp. strain IGTS8 possesses an enzymatic pathway that can remove covalently bound sulfur from dibenzothiophene (DBT) without breaking carbon-carbon bonds. The DNA sequence of a 4.0-kb BstBI-BsiWI fragment that carries the genes for this pathway was determined. Frameshift and
Olga E Eremina et al.
Carbohydrate polymers, 216, 260-269 (2019-05-03)
Solid-phase extraction of polycyclic aromatic sulfur heterocycles (PASHs) and their rapid determination in oil fuel without tedious sample pretreatment are of high interest. We propose porous and optically transparent hydrogels prepared from the covalently crosslinked chitosan (CS) as the basis
Karina Taciana Silva et al.
Journal of proteome research, 14(1), 385-396 (2014-11-05)
Dibenzothiophene (DBT) and its oxidized derivative dibenzothiophene sulfone (DBTO2) are important representatives of polycyclic aromatic hydrocarbons (PAHs). Due to the importance of PAHs in oncogenesis and the lack of toxicological investigations related to DBT and DBTO2, this work proposes to

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