Interesting facts
Interesting Facts about Dibenzothiophene
Dibenzothiophene is a fascinating compound that plays a significant role in several industrial applications and organic chemistry discussions. Here are some intriguing aspects of this compound:
- Structural Significance: Dibenzothiophene consists of two benzene rings fused to a thiophene ring, giving it a unique planar structure. This arrangement is key in defining its chemical properties and reactivity.
- Source and Extraction: It is commonly found in fossil fuels, particularly in crude oil and coal. Its presence is often used as an indicator of *aromatic sulfur compounds* in various petrochemical products.
- Environmental Impact: Dibenzothiophene, being a polycyclic aromatic sulfur heterocycle, raises environmental concerns due to its potential *toxicity* and *carcinogenic* properties. Awareness of these hazards is crucial for industries that handle it.
- Catalytic Potential: The compound is studied for its role in catalytic reactions, particularly in the *hydrodesulfurization* processes aimed at reducing sulfur content in fuels. Advances in this area can lead to more environmentally friendly fuel options.
- Analytical Chemistry: In analytical chemistry, dibenzothiophene is often used as a reference standard in chromatography techniques. Its structure allows for precise identification and quantification of similar compounds.
- Biological Applications: Research is ongoing into its potential medicinal properties, including anti-cancer and anti-microbial effects. Compounds like dibenzothiophene are being explored in the synthesis of novel pharmaceuticals.
In summary, dibenzothiophene is not just an ordinary compound; it holds a wealth of information that bridges chemistry, industry, and environmental science. As *Maria Curie* once said, “We must believe that we are gifted for something and that this thing, at whatever cost, must be attained.” In the world of dibenzothiophene, this relates to both the challenges and opportunities that arise in its study and application.
Synonyms
dibenzothiophene
132-65-0
Diphenylene sulfide
Dibenzo[b,d]thiophene
9-Thiafluorene
alpha-Thiafluorene
2,2'-Biphenylylene sulfide
Dibenzothiophene [USAN]
.alpha.-Thiafluorene
Dibenzo(b,d)thiophene
CCRIS 5307
[1,1'-Biphenyl]-2,2'-diyl sulfide
HSDB 7409
NSC 2843
NSC-2843
EINECS 205-072-9
UNII-Z3D4AJ1R48
MFCD00004969
(1,1'-Biphenyl)-2,2'-diyl sulfide
Z3D4AJ1R48
DTXSID0047741
CHEBI:23681
AI3-00043
Dibenzothiophene (USAN)
DIBENZOTHIOPHENE [HSDB]
DIBENZOTHIOPHENE [IARC]
DTXCID0027725
NSC2843
NCGC00094646-01
a-thiafluorene
Dibenzothiophene 10 microg/mL in Acetonitrile
DIBENZOTHIOPHENE (IARC)
C12H8S
Dibenzothiophene, analytical standard
(1,1'-Biphenyl)-2,2'-diyl sulphide
[1,1'-Biphenyl]-2,2'-diyl sulphide
CAS-132-65-0
Dibenzthiophene
9Thiafluorene
alphaThiafluorene
Diphenylene sulphide
Dibenzothiophene-Sulfur
Spectrum_000926
[1,2'-diyl sulfide
Dibenzothiophene, 98%
Spectrum2_001011
Spectrum3_000383
Spectrum4_000504
Spectrum5_000863
2,2'Biphenylylene sulfide
Dibenzothiophene, >=99%
Dibenzothiophene (Standard)
SCHEMBL13294
BSPBio_002165
KBioGR_001047
KBioSS_001406
BIDD:GT0331
DivK1c_000393
SPECTRUM1500235
SPBio_001161
DIBENZOTHIOPHENE [INCI]
CHEMBL219828
HMS501D15
HY-B0973R
KBio1_000393
KBio2_001406
KBio2_003974
KBio2_006542
KBio3_001385
NINDS_000393
HMS1920E12
HMS2091K22
HMS3652N11
Pharmakon1600-01500235
(1,1'Biphenyl)2,2'diyl sulfide
HY-B0973
Tox21_111308
Tox21_303415
CCG-40229
NSC756732
s4205
STK367232
AKOS000278427
Tox21_111308_1
AC-1025
CS-4462
FD05876
FD14022
NSC-756732
SB66387
IDI1_000393
NCGC00094646-02
NCGC00094646-03
NCGC00094646-04
NCGC00257449-01
AS-12976
SBI-0051339.P003
DB-042124
D0148
NS00003432
SW219819-1
EN300-20188
C20125
D03777
AB00051965_02
AB00051965_03
Dibenzothiophene, purified by sublimation, >=99%
Q544767
SR-05000002089
SR-05000002089-1
BRD-K46863940-001-04-7
BRD-K46863940-001-05-4
BRD-K46863940-001-06-2
Z104477204
8-thiatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),3,5,10,12-hexaene
205-072-9
83R
Solubility of Dibenzothiophene (C12H8S)
Dibenzothiophene is a fascinating organic compound that exhibits unique solubility characteristics. Understanding its solubility behavior is essential in various applications, especially in the fields of organic chemistry and materials science.
Key Points on Solubility:
In summary, dibenzothiophene's solubility profile indicates that it favors non-polar environments while showing limited compatibility with polar solvents. This behavior is crucial for its practical applications, such as in organic synthesis or its role as a model compound for studying sulfur-containing organic materials.