Home Other Building Blocks 1016-05-3
1016-05-3,MFCD00004970
Catalog No.:AA0004VK
1016-05-3 | Dibenzothiophene sulfone
Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$29.00   $20.00
- +
5g
95%
in stock  
$65.00   $45.00
- +
25g
98%
in stock  
$98.00   $69.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Q & A
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0004VK
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
Computed 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  

Synonyms
 
DBT-5,5-dioxide 
dibenzothiophene-5,5-dioxide 
dibenzothiophenesulfone 
DBTO2 
DIBENZOTHIOPHENE S,S-DIOXIDE 
IKJFYINYNJYDTA-UHFFFAOYSA-N 
NSC627707 
AK-88734 
Q-101162 
Dibenzosulfolane 
DBT-sulfone 
Dibenzo[b,d]thiophene5,5-dioxide 
1016-05-3 
EINECS 213-805-9 
ACMC-209vwr 
AI3-03709 
ChemDiv1_024727 
Dibenzothiophene,5-dioxide 
AC1L22QK 
Oprea1_807990 
SCHEMBL29481 
Dibenzothiophene,5,5-dioxide 
BIDD:GT0235 
Dibenzothiophene sulfone 
Dibenzothiophene sulfone, 97% 
Jsp000230 
DTXSID5074424 
CHEBI:90356 
CTK8B4602 
dibenzo[b,d]thiolene-5,5-dione 
HMS657D21 
ZINC404348 
KS-00000GS6 
ANW-45625 
Dibenzo[b,d]thiophene 5,5-dioxide 
c0058 
CD-905 
Dibenzo-[b,d]thiophene 5,5-dioxide 
dibenzo[b,d]thiophene, 5,5-dioxide 
MFCD00004970 
NSC406519 
AKOS000276649 
Dibenzo[b,d]thiophene 5,5-dioxide # 
AC-4874 
API0002311 
Dibenzothiophene-5,5-dioxide 
MCULE-6598952963 
NSC-406519 
NSC-627707 
OR51865 
RP12529 
VT20378 
AJ-22347 
AN-11558 
DS-18510 
ST080665 
Dibenzothiophene 5,5-dioxide 
SY036936 
ZB013494 
AX8014405 
DB-049812 
RT-004788 
ST2406780 
4CH-018299 
D4153 
FT-0655578 
X4123 
Dibenzothiophene, 5,5-dioxide 
MFCD00004970 (97%) 
C21150 
SR-01000510213 
I09-1173 
SR-01000510213-1 
InChI=1/C12H8O2S/c13-15(14)11-7-3-1-5-9(11)10-6-2-4-8-12(10)15/h1-8 
C12H8O2S 
ACN-S005215 
C12-H8-O2-S 
CID13908 
Dibenzothiophene dioxide 
ACN-031910 
Dibenzothiophene sulfone, 97% - 25G 25g 
31795-44-5 
Diphenylene sulfone 
Literature

Title: SAR of α7 nicotinic receptor agonists derived from tilorone: exploration of a novel nicotinic pharmacophore.

Journal: Bioorganic & medicinal chemistry letters 20120215

Title: The β phase formation limit in two poly(9,9-di-n-octylfluorene) based copolymers.

Journal: Macromolecular rapid communications 20110701

Title: π-conjugation and charge polarization in fluorene-dibenzothiophene-S,S-dioxide co-oligomers by Raman spectroscopy and quantum chemistry.

Journal: The Journal of chemical physics 20110128

Title: 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.

Journal: The Journal of organic chemistry 20101015

Title: The interplay of conformation and photophysical properties in deep-blue fluorescent oligomers.

Journal: Chemical communications (Cambridge, England) 20100714

Title: Dipolar stabilization of emissive singlet charge transfer excited states in polyfluorene copolymers.

Journal: The journal of physical chemistry. B 20080529

Title: Is there a homolytic substitution chemistry (SH2) of sulfones?

Journal: The Journal of organic chemistry 20050916

Title: Dibenzothiophene-S,S-dioxide-fluorene co-oligomers. Stable, highly-efficient blue emitters with improved electron affinity.

Journal: Chemical communications (Cambridge, England) 20050721

Title: Prediction of genotoxicity of chemical compounds by statistical learning methods.

Journal: Chemical research in toxicology 20050601

Title: Elucidation of the metabolic pathway of fluorene and cometabolic pathways of phenanthrene, fluoranthene, anthracene and dibenzothiophene by Sphingomonas sp. LB126.

Journal: Research in microbiology 20030401

Title: Elucidation of the metabolic pathway for dibenzothiophene desulphurization by Rhodococcus sp. strain IGTS8 (ATCC 53968).

Journal: Microbiology (Reading, England) 19970901

Title: Molecular mechanisms of biocatalytic desulfurization of fossil fuels.

Journal: Nature biotechnology 19961201

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Additional Info:
Q & A
Related Products