Interesting facts
Interesting Facts about 4-chloro-2-(5-chloro-2-hydroxy-phenyl)sulfanyl-phenol
This intriguing compound, known as a phenolic sulfide, exhibits a variety of fascinating properties and potential applications in both research and industrial contexts. Below are some captivating aspects of this compound:
- Biological Activity: Many derivatives of phenolic compounds, including sulfides, are known for their biological activities. This compound may share similarities that could lead to interesting studies in pharmacology, including potential antioxidant and antimicrobial properties.
- Synthetic Utility: The presence of both chloro and hydroxy groups increases the compound's reactivity, making it an excellent candidate for further chemical modifications. This opens up avenues for synthesizing new compounds that can be tailored for specific applications.
- Environmental Impact: Compounds with chlorinated elements often merit attention in environmental chemistry. Their behavior in biological systems and the environment raises critical questions about persistence and toxicity, crucial for environmental safety assessments.
- Structural Complexity: The intricate structure of this compound, featuring multiple functional groups, makes it an attractive subject for computational chemistry studies aimed at understanding reaction mechanisms and properties.
- Pharmaceutical Implications: Given its potential bioactivity, researchers might explore this compound for developing new therapeutic agents, particularly in treating conditions where phenolic compounds show promise.
In summary, 4-chloro-2-(5-chloro-2-hydroxy-phenyl)sulfanyl-phenol stands out not only for its unique structure but also for its potential implications in various scientific fields. As research progresses, it may unveil new properties and applications, bridging chemistry and biology in exciting ways.
Synonyms
Fenticlor
97-24-5
2,2'-THIOBIS(4-CHLOROPHENOL)
Bis(2-hydroxy-5-chlorophenyl) sulfide
Fentichlor
Novex
Phentichlorum
Meflorin
Ovitrol
Fenticloro
Oksid
Bis(2-hydroxy-5-chlorophenyl)sulfide
Fenticlorum
D 25-Antimykotikum
S 7 (antimycotic)
Phenol, 2,2'-thiobis[4-chloro-
2,2'-Dihydroxy-5,5'-dichlorodiphenyl sulfide
Ph 549
Caswell No. 851
2,2'-Dihydroxy-5,5'-dichlorophenyl sulfide
5,5'-Dichloro-2,2'-dihydroxydiphenyl sulfide
CR 305
Fenticlorum [INN-Latin]
Fenticloro [INN-Spanish]
HL 1050
NSC-4112
Phenol, 2,2'-thiobis(4-chloro-
2,2'-Thiobis4-chlorophenol
Fenticlor [USAN:INN:BAN]
NSC 55636
NSC-55636
2,2'-sulfanediylbis(4-chlorophenol)
CCRIS 4731
CHEBI:556580
D 25
4-chloro-2-(5-chloro-2-hydroxyphenyl)sulfanylphenol
NSC 4112
NSC55636
EINECS 202-568-7
EPA Pesticide Chemical Code 064209
BRN 2057140
2,2'-Thiobis[4-chlorophenol]
DTXSID4026137
S 7
AI3-08456
D61659OVD0
FENTICLOR [INN]
FENTICLOR [MI]
FENTICLOR [USAN]
FENTICLOR [MART.]
FENTICLOR [WHO-DD]
MLS002415676
DTXCID506137
NSC4112
4,4'-dichloro-2,2'-thiodiphenol
4-06-00-05645 (Beilstein Handbook Reference)
component of Banish
4-chloro-2-[(5-chloro-2-hydroxyphenyl)sulfanyl]phenol
Bis(5-chloro-2-hydroxyphenyl) Sulfide
NCGC00013679-02
SMR000145265
Fenticlorum (INN-Latin)
Fenticloro (INN-Spanish)
FENTICLOR (MART.)
2,5'-dichlorophenyl sulfide
2,5'-dichlorodiphenyl sulfide
Phenol,2'-thiobis[4-chloro-
WLN: QR DG BSR BQ EG
5,2'-dihydroxydiphenyl sulfide
Fentichlor; Fenticlor; HL 1050; Meflorin; NSC 4112
CAS-97-24-5
S-7
S 7 (VAN)
D 25 (VAN)
UNII-D61659OVD0
D 25Antimykotikum
MFCD00031479
Fenticlor (USAN/INN)
Epitope ID:131793
cid_7329
NCIStruc1_000386
NCIStruc2_000549
TimTec1_002292
4-chloro-2-(5-chloro-2-hydroxyphenylthio)phenol
Oprea1_024834
Oprea1_589846
SCHEMBL23276
2,2'Thiobis(4chlorophenol)
Phenol, 2,2'thiobis(4chloro
CHEMBL473535
4-chloro-2-(5-chloro-2-hydroxy-phenyl)sulfanyl-phenol
component of Banish (Salt/Mix)
ANUSOIHIIPAHJV-UHFFFAOYSA-
BDBM80984
Bis(2hydroxy5chlorophenyl)sulfide
Bis(2hydroxy5chlorophenyl) sulfide
HMS1540I04
KUC106499N
ALBB-012859
NCI55636
Tox21_110031
Tox21_200961
BBL003411
CCG-37773
NCGC00013679
STK048543
AKOS000491331
Tox21_110031_1
KSC-19-058
2,2'Dihydroxy5,5'dichlorophenyl sulfide
NCGC00013679-03
NCGC00013679-04
NCGC00013679-06
NCGC00091879-01
NCGC00091879-02
NCGC00258514-01
AS-13478
NCI60_004363
2,2'Dihydroxy5,5'dichlorodiphenyl sulfide
5,5'Dichloro2,2'dihydroxydiphenyl sulfide
DB-022656
B0850
NS00001597
2,2'-THIOBIS(4-CHLOROPHENOL) [INCI]
D04164
D88702
EN300-220348
SR-01000878241
4-chloro-2-[(5-chloro-2-hydroxyphenyl)thio]phenol
Q5443595
SR-01000878241-2
4-chloro-2-[(5-chloro-2-hydroxy-phenyl)thio]phenol
BRD-K19439093-001-01-0
Z57205386
4-chloranyl-2-(5-chloranyl-2-oxidanyl-phenyl)sulfanyl-phenol
202-568-7
InChI=1/C12H8Cl2O2S/c13-7-1-3-9(15)11(5-7)17-12-6-8(14)2-4-10(12)16/h1-6,15-16H
Solubility of 4-chloro-2-(5-chloro-2-hydroxy-phenyl)sulfanyl-phenol
The solubility of 4-chloro-2-(5-chloro-2-hydroxy-phenyl)sulfanyl-phenol, also known as chlorosulfanyl-phenol, can be quite complex due to its multi-functional nature. This compound possesses both hydrophilic and hydrophobic characteristics, making it of particular interest in various chemical applications.
Factors influencing its solubility include:
In summary, while 4-chloro-2-(5-chloro-2-hydroxy-phenyl)sulfanyl-phenol is expected to show moderate solubility in polar organic solvents and perhaps limited solubility in water, it is pivotal to conduct empirical solubility tests for precise applications. As noted, one should consider the diverse interactions at play and how they contribute to the overall solubility dynamics of this unique compound.