Home Sulfos Dibenzothiophene sulfone

Dibenzothiophene sulfone

CAS No.:
1016-05-3
Catalog Number:
AG0004YC
Molecular Formula:
C12H8O2S
Molecular Weight:
216.2557
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$25
- +
5g
95%
In Stock USA
United States
$57
- +
10g
95%
In Stock USA
United States
$90
- +
25g
95%
In Stock USA
United States
$169
- +
100g
95%
In Stock USA
United States
$513
- +
Product Description
Catalog Number:
AG0004YC
Chemical Name:
Dibenzothiophene sulfone
CAS Number:
1016-05-3
Molecular Formula:
C12H8O2S
Molecular Weight:
216.2557
MDL Number:
MFCD00004970
IUPAC Name:
dibenzothiophene 5,5-dioxide
InChI:
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
SMILES:
O=S1(=O)c2ccccc2c2c1cccc2
EC Number:
213-805-9
Properties
Complexity:
313  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
216.025g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
216.254g/mol
Monoisotopic Mass:
216.025g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
42.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.4  
Literature
Title Journal
SAR of α7 nicotinic receptor agonists derived from tilorone: exploration of a novel nicotinic pharmacophore. Bioorganic & medicinal chemistry letters 20120215
The β phase formation limit in two poly(9,9-di-n-octylfluorene) based copolymers. Macromolecular rapid communications 20110701
π-conjugation and charge polarization in fluorene-dibenzothiophene-S,S-dioxide co-oligomers by Raman spectroscopy and quantum chemistry. The Journal of chemical physics 20110128
Tuning the intramolecular charge transfer emission from deep blue to green in ambipolar systems based on dibenzothiophene S,S-dioxide by manipulation of conjugation and strength of the electron donor units. The Journal of organic chemistry 20101015
The interplay of conformation and photophysical properties in deep-blue fluorescent oligomers. Chemical communications (Cambridge, England) 20100714
Dipolar stabilization of emissive singlet charge transfer excited states in polyfluorene copolymers. The journal of physical chemistry. B 20080529
Is there a homolytic substitution chemistry (SH2) of sulfones? The Journal of organic chemistry 20050916
Dibenzothiophene-S,S-dioxide-fluorene co-oligomers. Stable, highly-efficient blue emitters with improved electron affinity. Chemical communications (Cambridge, England) 20050721
Prediction of genotoxicity of chemical compounds by statistical learning methods. Chemical research in toxicology 20050601
Elucidation of the metabolic pathway of fluorene and cometabolic pathways of phenanthrene, fluoranthene, anthracene and dibenzothiophene by Sphingomonas sp. LB126. Research in microbiology 20030401
Elucidation of the metabolic pathway for dibenzothiophene desulphurization by Rhodococcus sp. strain IGTS8 (ATCC 53968). Microbiology (Reading, England) 19970901
Molecular mechanisms of biocatalytic desulfurization of fossil fuels. Nature biotechnology 19961201
Properties