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Sulconazole

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Identification
Molecular formula
C21H20ClNO3S2P
CAS number
831-61-8
IUPAC name
(4-chlorophenyl)sulfanylmethylsulfanyl-diethoxy-thioxo-lambda5-phosphane
State
State

At room temperature, Sulconazole is in a solid state, typically found in the form of a powder. Because of its solid form, it is usually handled in a powdered condition for pharmaceutical formulations.

Melting point (Celsius)
121.00
Melting point (Kelvin)
394.15
Boiling point (Celsius)
463.00
Boiling point (Kelvin)
736.15
General information
Molecular weight
387.91g/mol
Molar mass
387.9140g/mol
Density
1.4245g/cm3
Appearence

Sulconazole appears as a white to pale yellow crystalline powder. It is a crystalline compound that can vary slightly in color from white to yellow depending on its purity and exposure to light.

Comment on solubility

Solubility of (4-chlorophenyl)sulfanylmethylsulfanyl-diethoxy-thioxo-lambda5-phosphane

The solubility of (4-chlorophenyl)sulfanylmethylsulfanyl-diethoxy-thioxo-lambda5-phosphane in various solvents is a nuanced subject that depends on its molecular structure and intermolecular interactions.

  • Polar Solvents: Compounds with polar characteristics often exhibit better solubility in polar solvents like water and alcohols. However, due to the presence of sulfur and phosphorus, one might expect limited solubility in water, making alcohol-based solutions more favorable.
  • Non-Polar Solvents: Conversely, non-polar solvents such as hexane or toluene may provide a more suitable environment for solubility due to reduced polarity interactions.
  • Solvent Compatibility: Compatibility with a solvent can be gauged by considering functional groups. The presence of ethoxy groups may enhance solubility in organic solvents.

In conclusion, the solubility of (4-chlorophenyl)sulfanylmethylsulfanyl-diethoxy-thioxo-lambda5-phosphane is influenced by its intricate structural features, leading to varied solubility patterns based on the solvent polarity. As a general guideline, whenever exploring its solubility, one might refer to the hierarchy:

  1. Test solubility in polar solvents.
  2. If limited, proceed to consider non-polar solvents.
  3. Evaluate hybrid solvent systems as a potential solution.

Ultimately, conducting experimental solubility tests is recommended to acquire accurate data tailored to the compound's unique characteristics.

Interesting facts

Interesting Facts about (4-chlorophenyl)sulfanylmethylsulfanyl-diethoxy-thioxo-lambda5-phosphane

(4-chlorophenyl)sulfanylmethylsulfanyl-diethoxy-thioxo-lambda5-phosphane, a complex organophosphorus compound, showcases the fascinating interplay of sulfur and phosphorus in its structure and reactivity. This molecule draws attention for several reasons:

  • Sulfur Complexity: The presence of multiple sulfur atoms (in both sulfanyl and thioxo forms) hints at intriguing properties, including potential nucleophilicity and reactivity in various chemical reactions.
  • Phosphorus as a Functional Group: The lambda5-phosphane core in the compound indicates that it is part of a wider class of compounds known as phosphines, which are pivotal in organic synthesis and coordination chemistry.
  • Biological Relevance: Organophosphorus compounds often exhibit biological activities, making them interesting candidates for drug development and agricultural applications.
  • Chlorine Influence: The presence of a chlorophenyl group can enhance the lipophilicity of the compound, which may affect its interaction with biological membranes and its overall biological profile.
  • Synthetic Versatility: Such compounds can be utilized in a multitude of reactions, including coupling reactions, which makes them valuable in synthesizing larger, more complex molecules.

With these characteristics, (4-chlorophenyl)sulfanylmethylsulfanyl-diethoxy-thioxo-lambda5-phosphane not only stands out in the realm of synthetic chemistry but also serves as a key point of exploration for researchers investigating the properties of phosphorus-sulfur systems. Its synthesis and subsequent applications may contribute valuable insights into the potential uses of phosphorus compounds in medicine and industry.

Synonyms
CARBOPHENOTHION
Carbofenotion
786-19-6
Carbofenotion [INN]
Caswell No. 165
Carbofenotionum [INN-Latin]
Stauffer R-1303
HSDB 958
Trithiontylphenol
EINECS 212-324-1
EPA Pesticide Chemical Code 058102
NSC-231691
UNII-998NGA2Q61
BRN 1885240
DTXSID7022120
CHEBI:82107
AI3-23708
Carbophenothion [ANSI:BSI:ISO]
Carbofenotion [INN:BAN]
Carbophenothion [INN:ANSI:BSI:ISO]
CARBOPHENOTHION [MI]
CARBOPHENOTHION [ISO]
CARBOPHENOTHION [HSDB]
DTXCID002120
O,O-Diethyl S-(p-Chlorophenylthio)methyl phosphorodithioate
S-((p-Chlorophenylthio)methyl) O,O-diethyl phosphorodithioate
O,O-Diethyl-S-((4-chloor-fenyl-thio)-methyl)-dithiofosfaat [Dutch]
O,O-Diaethyl-S-((4-chlor-phenyl-thio)-methyl)dithiophosphat [German]
O,O-Diaethyl-S-((4-chlor-phenyl-thio)-methyl)dithiophosphat
O,O-Diethyl-S-((4-chloor-fenyl-thio)-methyl)-dithiofosfaat
Carbofenotionum (INN-Latin)
O,O-Diethyl-S-(4-chloor-fenyl-thio)-methyl)-dithiofosfaat
S-(4-Chlorophenylthiomethyl) OO-diethyl phosphorodithioate
Carbophenothion (ANSI:BSI:ISO)
O,O-Diaethyl-S-((4-chlor-phenyl-thio)methyl)dithiophosphat
O,O-Diethyl S-(((4-chlorophenyl)thio)methyl) dithiophosphate
O,O-Diethyl S-(((p-chlorophenyl)thio)methyl) dithiophosphate
O,O-Diethyl (((p-chlorophenyl)mercapto)methyl) dithiophosphate
S-(((4-Chlorophenyl)thio)methyl)diethyl phosphorothiolothionate
Carbophenothion (INN:ANSI:BSI:ISO)
Stauffer R 1303
O,O-Diaethyl-S-[(4-chlor-phenyl-thio)methyl]dithiophosphat
O,O-Diethyl [[(p-chlorophenyl)mercapto]methyl] dithiophosphate
O,O-Diethyl S-[[(4-chlorophenyl)thio]methyl] dithiophosphate
O,O-Diethyl S-[[(p-chlorophenyl)thio]methyl] dithiophosphate
S-[[(4-Chlorophenyl)thio]methyl]diethyl phosphorothiolothionate
PHOSPHORODITHIOIC ACID,S-(((4-CHLOROPHENYL)THIO)METHYL) O,O-DIETHYL ESTER
PHOSPHORODITHIOIC ACID,S-[[(4-CHLOROPHENYL)THIO]METHYL] O,O-DIETHYL ESTER
Stauffer R1,303
R 1303 (PESTICIDE)
S-(((p-chlorophenyl) thio)methyl O,O-diethyl phosphorodithioate)
R1303
O,ODietilS((4clorofeniltio)metile)ditiofosfato
O,ODiethyl Spchlorophenylthiomethyl dithiophosphate
O,ODiethylS((4chloorfenylthio)methyl)dithiofosfaat
O,ODiaethylS((4chlorphenylthio)methyl)dithiophosphat
O,ODiethyl pchlorophenylmercaptomethyl dithiophosphate
O,ODiethyl S(4chlorophenylthiomethyl) dithiophosphate
O,ODiethyl S(pchlorophenylthiomethyl) phosphorodithioate
S(4Chlorophenylthiomethyl)diethyl phosphorothiolothionate
S((pChlorophenylthio)methyl) O,Odiethyl phosphorodithioate
O,ODiethyl dithiophosphoric acid pchlorophenylthiomethyl ester
O,ODiethylSpchlorfenylthiomethylester kyseliny dithiofosforecne
S(((4Chlorophenyl)thio)methyl) O,Odiethyl phosphorodithioate
Dithiophosphate de O,Odiethyle et de (4chlorophenyl) thiomethyle
S(((4Chlorophenyl)thio)methyl) O,Odiethyl phosphorodithioate (9CI)
S-(4-CHLOROPHENYLTHIOMETHYL) DIETHYL PHOSPHOROTHIOLOTHIONATE
O,O-DIAETHYL-S-((4-CHLOR-PHENYL-THIO)METHYL)DITHIOPHOSPHAT (GERMAN)
O,O-DIETHYL-S-(4-CHLOOR-FENYL-THIO)-METHYL)-DITHIOFOSFAAT (DUTCH)
Phosphorodithioic acid, S(((4chlorophenyl)thio)methyl) O,Odiethyl ester
Phosphorodithioic acid, S(((pchlorophenyl)thio)methyl) O,Odiethyl ester
4-06-00-01595 (beilstein handbook reference)
un3018
vedtxtnsfwuxgq-uhfffaoysa-n
Oleoakarithion
Trithion
Dagadip
Carbofenothion
Carbofenthion
Acarithion
Garrathion
Hexathion
Akarithion
Nephocarp
Ethyl carbophenothion
Trithion miticide
Lethox
Endyl
Karbofenothion
Stauffer R-1,303
R 1303
R-1303
ENT 23,708
NSC 231691
OMS 244
O,O-Diethyl dithiophosphoric acid p-chlorophenylthiomethyl ester
Phosphorodithioic acid, S-(((4-chlorophenyl)thio)methyl) O,O-diethyl ester
998NGA2Q61
Dithiophosphate de O,O-diethyle et de (4-chloro-phenyl) thiomethyle
O,O-Diethyl-S-p-chlorfenylthiomethylester kyseliny dithiofosforecne
O,O-Dietil-S-((4-cloro-fenil-tio)-metile)-ditiofosfato
NCGC00166170-01
S-(((4-Chlorophenyl)thio)methyl) O,O-diethyl phosphorodithioate
S-(((p-Chlorophenyl)thio)methyl) O,O-diethyl phosphorodithioate
S-[[(p-Chlorophenyl)thio]methyl] O,O-diethyl phosphorodithioate
Phosphorodithioic acid, S-(((p-chlorophenyl)thio)methyl) O,O-diethyl ester
Carbofenotionum
Carbofenothion [Dutch]
Karbofenothion [Czech]
Phosphorodithioic acid, S-[[(4-chlorophenyl)thio]methyl] O,O-diethyl ester
Phosphorodithioic acid, S-[[(p-chlorophenyl)thio]methyl] O,O-diethyl ester
CAS-786-19-6
O,O-Diethyl S-p-chlorophenylthiomethyl dithiophosphate
O,O-Diethyl p-chlorophenylmercaptomethyl dithiophosphate
O,O-Diethyl S-(4-chlorophenylthiomethyl) dithiophosphate
S-(4-Chlorophenylthiomethyl)diethyl phosphorothiolothionate
Carbophenothion solution
O,O-Diethyl S-(p-chlorophenylthiomethyl) phosphorodithioate
O,O-Dietil-S-((4-cloro-fenil-tio)-metile)-ditiofosfato [Italian]
Dithiophosphate de O,O-diethyle et de (4-chloro-phenyl) thiomethyle [French]
O,O-Diethyl-S-p-chlorfenylthiomethylester kyseliny dithiofosforecne [Czech]
SCHEMBL10754
Carbofenotion, Carbophenothion
MLS004712086
CHEMBL452866
S-{[(4-chlorophenyl)thio]methyl} O,O-diethyl dithiophosphate
Tox21_113359
Tox21_301426
MFCD00128009
NSC231691
NCGC00166170-02
NCGC00255134-01
SMR001550569
WLN: 2OPS&O2&SR D1SPS&O2&O2
Carbophenothion 10 microg/mL in Isooctane
DB-056319
NS00015384
Carbophenothion 100 microg/mL in Cyclohexane
C18968
Carbophenothion, PESTANAL(R), analytical standard
SR-01000883724
Q2937964
SR-01000883724-1
s-4-chlorophenylthiomethyl o,o-diethyl phosphorodithioate
O,O-Diethyl S-[[(p-chlorophenyl)thio]methyl] phosphorodithioate
S-([(4-Chlorophenyl)sulfanyl]methyl) O,O-diethyl dithiophosphate #
(4-chlorophenyl)sulfanylmethylsulfanyl-diethoxy-sulfanylidene-?5-phosphane
(4-chlorophenyl)sulfanylmethylsulfanyl-diethoxy-sulfanylidene-lambda5-phosphane