Interesting facts
Interesting Facts about 2,4-Dichloro-6-(3,5-dichloro-2-hydroxy-phenyl)sulfanyl-phenol
2,4-Dichloro-6-(3,5-dichloro-2-hydroxy-phenyl)sulfanyl-phenol is a fascinating compound with a variety of applications and characteristics that make it noteworthy in the field of chemistry. Here are some engaging facts that highlight its importance:
- Complex Structure: This compound features a complex molecular structure that includes multiple chlorine atoms and phenolic groups. The presence of the sulfanyl group adds to its unique reactivity.
- Biological Significance: Compounds like this often exhibit biological properties, making them valuable in pharmacology and biochemistry. Their derivatives can act as antimicrobial agents or even potential pharmaceuticals.
- Environmental Impact: Its structure suggests potential uses in environmental chemistry, particularly in understanding pollutant degradation or in the development of herbicides and pesticides.
- Research Potential: Ongoing research could unveil new applications or effects of this compound. Scientists might investigate its interaction with various biological systems, which can lead to exciting discoveries in medicinal chemistry.
- Synthesis Challenges: The synthesis of such a compound can be quite intricate, often requiring advanced techniques in organic chemistry for successful execution. This serves as an excellent case study for students and chemists alike.
In summary, 2,4-dichloro-6-(3,5-dichloro-2-hydroxy-phenyl)sulfanyl-phenol is not just a compound with an interesting construction; it has implications across several fields, showcasing the profound connection between chemistry and technology. The potential for new discoveries stemming from this compound is vast and ripe for exploration.
Synonyms
bithionol
97-18-7
2,2'-Thiobis(4,6-dichlorophenol)
Bithin
Lorothidol
Actamer
Bitionol
Bithionol sulfide
Bithionolate
Bidiphen
Bisoxyphen
Lorothiodol
Bitin
Neopellis
Nobacter
Vancide BL
Usaf B-22
Bithional
2-Hydroxy-3,5-dichlorophenyl sulfide
Bis(2-hydroxy-3,5-dichlorophenyl) sulfide
TKhsd
Bis(3,5-dichloro-2-hydroxyphenyl) sulfide
2,2'-sulfanediylbis(4,6-dichlorophenol)
XEROSIN
XL 7
2-Hydroxy-3,5-dichlorophenyl sulphide
2,2'-Dihydroxy-3,3',5,5'-tetrachlorodiphenyl sulfide
6,6'-thiobis(2,4-dichlorophenol)
2,4-dichloro-6-(3,5-dichloro-2-hydroxyphenyl)sulfanylphenol
CP 3438
D 26
NCI-C60628
NSC 47129
2,2'-Dihydroxy-3,3',5,5'-tetrachlorodiphenylsulfide
MFCD00055727
NSC-47129
Phenol, 2,2'-thiobis(4,6-dichloro-
Phenol, 2,2'-thiobis[4,6-dichloro-
AMT77LS62O
MLS000028403
CHEBI:3131
XL-7
1394-04-3
DTXSID9021342
2,2'-Thiobis[4,6-dichlorophenol]
NCGC00018163-06
Bithionolum
SMR000058374
2,4-dichloro-6-(3,5-dichloro-2-hydroxy-phenyl)sulfanyl-phenol
Caswell No. 852
Bitionol [INN-Spanish]
Bithionolum [INN-Latin]
DTXCID701342
Phenol,2'-thiobis[4,6-dichloro-
WLN: QR BG DG FSR BQ CG EG
2,3',5,5'-tetrachlorodiphenyl sulfide
CAS-97-18-7
CCRIS 2043
HSDB 6380
EINECS 202-565-0
UNII-AMT77LS62O
EPA Pesticide Chemical Code 064201
BRN 2003535
AI3-50518
Bithionol [INN:BAN:JAN:NF]
B1T
Bithin (TN)
2,2'-Thio-bis(4,6-dichlorophenol)
Bithionol (Standard)
Spectrum_000088
Bithionol (JAN/INN)
BITHIONOL [INN]
BITHIONOL [JAN]
BITHIONOL [MI]
BITHIONOL [HSDB]
Spectrum2_000113
Spectrum3_000319
Spectrum4_000257
Spectrum5_000922
BITHIONOL [MART.]
BITHIONOL [WHO-DD]
cid_2406
Oprea1_473080
REGID_for_CID_2406
SCHEMBL64385
BSPBio_001918
KBioGR_000694
KBioSS_000508
DivK1c_000639
SPBio_000126
CHEMBL290106
GTPL2338
Bithionol, >=98% (HPLC)
BDBM36880
HMS501P21
JFIOVJDNOJYLKP-UHFFFAOYSA-
KBio1_000639
KBio2_000508
KBio2_003076
KBio2_005644
KBio3_001418
NSC9872
NINDS_000639
KUC106451N
NSC-9872
NSC47129
Tox21_110832
Tox21_200384
Tox21_302919
HY-17592R
s4552
STL257451
AKOS015856712
Tox21_110832_1
CCG-268103
CS-3874
DB04813
KSC-19-055
IDI1_000639
QTL1_000014
NCGC00018163-01
NCGC00018163-02
NCGC00018163-03
NCGC00018163-04
NCGC00018163-05
NCGC00018163-07
NCGC00018163-08
NCGC00018163-09
NCGC00018163-10
NCGC00021272-04
NCGC00021272-05
NCGC00021272-06
NCGC00256573-01
NCGC00257938-01
BS-18280
DA-71563
HY-17592
Inh 2 [PMID: 32284327]
SBI-0051298.P003
NS00011716
T0865
Bithionol, VETRANAL(TM), analytical standard
C07967
C77336
D00802
EN300-18531364
Q4918862
BRD-K39120595-304-03-9
BRD-K39120595-304-04-7
2,4-dichloro-6-[(3,5-dichloro-2-hydroxy-phenyl)thio]phenol
2,4-dichloro-6-[(3,5-dichloro-2-hydroxyphenyl)sulfanyl]phenol
2,4-dichloro-6-[(3,5-dichloro-2-hydroxyphenyl)thio]phenol
2-[3,5-bis(chloranyl)-2-oxidanyl-phenyl]sulfanyl-4,6-bis(chloranyl)phenol
InChI=1/C12H6Cl4O2S/c13-5-1-7(15)11(17)9(3-5)19-10-4-6(14)2-8(16)12(10)18/h1-4,17-18H
Solubility of 2,4-Dichloro-6-(3,5-Dichloro-2-Hydroxy-Phenyl)Sulfanyl-Phenol (C18H10Cl4O2)
The solubility of 2,4-dichloro-6-(3,5-dichloro-2-hydroxy-phenyl)sulfanyl-phenol can be quite intricate due to its complex molecular structure. Generally, the solubility of organic compounds is influenced by various factors such as polarity, molecular weight, and presence of functional groups.
Solubility Characteristics:
In practical terms, it is likely that 2,4-dichloro-6-(3,5-dichloro-2-hydroxy-phenyl)sulfanyl-phenol is:
As with many chemical compounds, environmental conditions such as temperature and pH can also play significant roles in solubility behavior. Understanding the solubility of this compound is crucial for applications in various fields, including pharmaceuticals and materials science.