Interesting facts
Interesting Facts about (4-chlorophenyl) 4-chlorobenzenesulfonate
(4-chlorophenyl) 4-chlorobenzenesulfonate, often referred to in the realm of organic chemistry, is a fascinating compound that holds significant importance in various chemical fields. Here are some engaging insights:
- Applications in Synthesis: This compound serves as an essential building block in the synthesis of more complex organic molecules. Its functionalization allows chemists to explore new reactions and formulations.
- Role as a Leaving Group: The sulfonate moiety in this compound acts as a good leaving group, which promotes nucleophilic substitution reactions. This property is highly valued in the development of pharmaceuticals and agrochemicals.
- Toxicological Considerations: The presence of chlorine substituents raises some interesting discussions surrounding environmental toxicity and biological interactions, necessitating caution in its handling and usage.
- Structural Features: The compound exhibits a biphenyl structure that can influence its reactivity and interactions with other substances, leading to unique properties that are of great interest in materials science.
- Research Frontiers: Scientists continue to study the implications of compounds like (4-chlorophenyl) 4-chlorobenzenesulfonate in drug design and environmental chemistry.
In summary, (4-chlorophenyl) 4-chlorobenzenesulfonate is not just a compound with varied applications; it is a portal into the complexities of organic synthesis, toxicology, and environmental impact. Understanding compounds like this one expands our knowledge and capabilities in both scientific research and practical applications.
Synonyms
Chlorfenson
Ovex
80-33-1
Difenson
Orthotran
Ovochlor
Ester sulfonate
Benzolsulfonate
Chlorofenizon
Ephirsulphonate
Ethersulfonate
Trichlorfenson
Chlorfensin
Corotran
Estonmite
Niagaratran
Orochlor
Sappilan
Sappiran
Erysit
Otracid
Ovatran
Ovotox
Ovotran
CPCBS
Chloorfenson
Chlorofensone
Danicut
Acaricydol E 20
Lethalaire G-58
4-CHLOROPHENYL 4-CHLOROBENZENESULFONATE
Chlorobenzolsulfonate
PCPCBS
Miticide K-101
Genite 883
Chlorfensonchlorofensone
Benzolsulfonat
Chlorefenizon
Chlorofenson
ONEX
Chlorbenzolsulfonat
Ovatron
Chloorfenson [Dutch]
Caswell No. 624
Ovex [ANSI]
Chlorefenizon [French]
Trichlorfenson (Obs.)
Chlorfenson [BSI:ISO]
p-Chlorophenyl p-chlorobenzenesulfonate
Benzenesulfonic acid, 4-chloro-, 4-chlorophenyl ester
C-854
D 854
Dow K-6,451
K 6451
p-Chlorophenyl p-chlorobenzenesulphonate
4-Chlorophenyl 4-chlorobenzenesulphonate
HSDB 2055
C 1,006
p-Chlorobenzenesulfonic acid, p-chlorophenyl ester
(4-chlorophenyl) 4-chlorobenzenesulfonate
LW65NJ3YWV
(4-Cloro-fenil)-4-cloro-venzol-solfonato
Parachlorophenyl-parachlorobenzene-sulfonate
(4-Chlor-phenyl)-4-chlor-benzol-sulfonate
4-Chlorobenzenesulfonate de 4-chlorophenyle
NSC 5618
K-101
EINECS 201-270-4
(4-Chloor-fenyl)-4-chloor-benzeen-sulfonaat
4-Chlorphenyl-4'-chlorbenzolsulfonat
ENT 16,358
ENT 16,538
EPA Pesticide Chemical Code 020201
BRN 2944674
DTXSID5020310
AI3-16538
Benzenesulfonic acid, p-chloro-, p-chlorophenyl ester
Parachlorophenyl parachlorobenzene sulfonate
CHLORFENSON [MI]
4-Chlorphenyl-4'-chlorbenzolsulfonat [German]
CHLORFENSON [ISO]
CHLORFENSON [HSDB]
p-Chlorfenylester kyseliny p-chlorbenzensulfonove
4-Chlorobenzenesulfonic acid, 4-chlorophenyl ester
4-Chlorobenzenesulfonate de 4-chlorphenyle [French]
p-Chlorophenyl-p-chlorobenzene sulfonate
(4-Chloor-fenyl)-4-chloor-benzeen-sulfonaat [Dutch]
(4-Chlor-phenyl)-4-chlor-benzol-sulfonate [German]
(4-Cloro-fenil)-4-cloro-venzol-solfonato [Italian]
4-Chlorobenzenesulfonate de 4-chlorophenyle [French]
DTXCID50310
4-Chlorobenzenesulfonate de 4-chlorphenyle
p-Chlorfenylester kyseliny p-chlorbenzensulfonove [Czech]
CCS
CHEBI:82155
4-11-00-00109 (Beilstein Handbook Reference)
NSC-5618
Ovex (ANSI)
Chlorefenizon (French)
CHLOORFENSON (DUTCH)
CAS-80-33-1
4-Chlorobenzenesulfonate de 4-chlorphenyle (French)
UNII-LW65NJ3YWV
(4-CHLOR-PHENYL)-4-CHLOR-BENZOL-SULFONATE (GERMAN)
(4-CLORO-FENIL)-4-CLORO-VENZOL-SOLFONATO (ITALIAN)
4-CHLOROBENZENESULFONATE DE 4-CHLOROPHENYLE (FRENCH)
Lethalaire G58
Miticide K101
WLN: GR DSWOR DG
Dow K6,451
SCHEMBL116752
CHEMBL499017
4Chlorphenyl4'chlorbenzolsulfonat
RZXLPPRPEOUENN-UHFFFAOYSA-
NSC5618
(4Clorofenil)4clorovenzolsolfonato
(4Chlorphenyl)4chlorbenzolsulfonate
pChlorophenyl pchlorobenzenesulfonate
4Chlorophenyl 4chlorobenzenesulfonate
Tox21_201263
Tox21_302742
(4Chloorfenyl)4chloorbenzeensulfonaat
pChlorophenyl pchlorobenzenesulphonate
4Chlorophenyl 4chlorobenzenesulphonate
AKOS028110676
DB05377
4Chlorobenzenesulfonate de 4chlorphenyle
Parachlorophenylparachlorobenzenesulfonate
4-Chlorophenyl-4-chlorobenzene sulfonate
4Chlorobenzenesulfonate de 4chlorophenyle
NCGC00249010-01
NCGC00256598-01
NCGC00258815-01
4-chlorophenyl 4-chlorobenzene-1-sulfonate
HY-121157
CS-0079565
NS00005538
pChlorfenylester kyseliny pchlorbenzensulfonove
C19024
Chlorfenson, PESTANAL(R), analytical standard
pChlorobenzenesulfonic acid, pchlorophenyl ester
4Chlorobenzenesulfonic acid, 4chlorophenyl ester
Benzenesulfonic acid, 4chloro, 4chlorophenyl ester
Benzenesulfonic acid, pchloro, pchlorophenyl ester
Benzenesulfonic acid, p-chloro-, p-chlorophenylester
Q2964122
BRD-K89409436-001-01-4
Benzenesulfonic acid, p-chloro-, p-chlorophenyl ester (8CI)
201-270-4
InChI=1/C12H8Cl2O3S/c13-9-1-5-11(6-2-9)17-18(15,16)12-7-3-10(14)4-8-12/h1-8H
Solubility of (4-chlorophenyl) 4-chlorobenzenesulfonate
(4-chlorophenyl) 4-chlorobenzenesulfonate, a compound known for its unique chemical structure, presents interesting characteristics regarding its solubility.
Typically, the solubility of such sulfonate compounds can be influenced by several factors, including:
While general trends suggest that sulfonate esters tend to be soluble in polar solvents, the specific solubility of (4-chlorophenyl) 4-chlorobenzenesulfonate can vary. Experimental data is essential for precise solubility determinations. In practical applications, it's crucial to consider:
In summary, understanding the solubility of (4-chlorophenyl) 4-chlorobenzenesulfonate is not just about its physical properties, but also its behavior in different chemical environments, making it a fascinating subject for study.