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Chlorophthalimide methylphenylphosphinothioate

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Identification
Molecular formula
C16H19ClNO4PS
CAS number
5000-08-4
IUPAC name
2-(2-chloro-1-diethoxyphosphinothioylsulfanyl-ethyl)isoindoline-1,3-dione
State
State

At room temperature, this compound is typically found in a solid state, characterized by its crystalline form. It is generally stable under recommended storage conditions.

Melting point (Celsius)
109.50
Melting point (Kelvin)
382.65
Boiling point (Celsius)
452.60
Boiling point (Kelvin)
725.75
General information
Molecular weight
374.84g/mol
Molar mass
374.8400g/mol
Density
1.3780g/cm3
Appearence

The compound is typically a crystalline solid, often appearing as a white to off-white powder, depending on the purity and specific form. It may exhibit a slightly yellowish hue if impurities are present.

Comment on solubility

Solubility of 2-(2-chloro-1-diethoxyphosphinothioylsulfanyl-ethyl)isoindoline-1,3-dione

The solubility of 2-(2-chloro-1-diethoxyphosphinothioylsulfanyl-ethyl)isoindoline-1,3-dione, with the chemical formula C16H19ClNO4PS, can be quite nuanced due to the presence of multiple functional groups within its structure. Here are some key considerations regarding its solubility:

  • Polarity: The compound has regions that can interact with polar solvents because of the presence of nitrogen, oxygen, and phosphorus atoms, making it potentially soluble in polar solvents such as water and alcohols.
  • Hydrophobic Interactions: The hydrocarbon portions of the molecule may impart some hydrophobic characteristics, suggesting limited solubility in purely polar solvents.
  • Common Solvents: It is likely to have better solubility in organic solvents, such as chloroform or acetone, due to the structural composition.
  • Temperature Effects: Like many compounds, solubility can increase with temperature, enhancing interactions between molecules and solvent molecules.
  • pH Sensitivity: The solubility may also vary with pH; substances containing acidic or basic functional groups can exhibit more solubility in specific pH environments.

While the exact solubility data of this compound may not be readily available, the multifaceted nature of its structure suggests that careful evaluation through solubility studies would provide valuable insights into its behavior in various solvent systems. As such, experiments could help to clarify the optimal conditions for dissolution.

Interesting facts

Interesting Facts About 2-(2-Chloro-1-diethoxyphosphinothioylsulfanyl-ethyl)isoindoline-1,3-dione

This intriguing compound, known as a derivative of isoindoline-1,3-dione, contains a complex set of functional groups that make it a point of interest in the fields of organic synthesis and medicinal chemistry. Here are some fascinating points about this compound:

  • Chlorine Power: The presence of chlorine in its structure is noteworthy. This halogen can enhance biological activity and increase lipophilicity, making the compound more suitable for certain applications.
  • Phosphorus Compounds: The incorporation of phosphorous in organic molecules often leads to interesting properties, such as enhanced catalytic behavior and potential as bioactive compounds.
  • Thiol Groups: The thioyl group is of significant importance as it may bestow unique reactivity. Thiol compounds are often involved in redox reactions, adding to the compound's potential in various chemical processes.
  • Applications in Medicine: Compounds of this nature have been researched for their potential use as pharmacologically active agents, particularly in the development of novel therapeutic drugs.
  • Synthetic Pathways: Its complex structure opens doors to interesting synthetic pathways, allowing chemists to explore various reaction mechanisms and compound transformations in the laboratory.

Furthermore, projects involving this compound can lead to discoveries that challenge or enhance existing methodologies in organic chemistry. As the saying goes in scientific research, "The boundaries of chemistry are always expanding." This compound exemplifies that with its challenging complexity and promising potential.

Synonyms
Dialifos
DIALIFOR
10311-84-9
Caswell No. 280A
Dialiphos [ISO-French]
Dialifor [ANSI:BSI:ISO]
HSDB 1559
EINECS 233-689-3
EPA Pesticide Chemical Code 102501
UNII-8480K0VB4E
BRN 1550800
O,O-Diethyl S-(2-chloro-1-phthalimidoethyl)phosphorodithioate
DTXSID0037522
AI3-27320
8480K0VB4E
DIALIFOS [HSDB]
DIALIFOR [ISO]
DIALIFOR [MI]
DTXCID8017522
Dialiphos (ISO-French)
Dialifor (ANSI:BSI:ISO)
PHTHALIMIDE, N-(2-CHLORO-1-MERCAPTOETHYL)-, S-ESTER WITH O,O-DIETHYL PHOSPHORODITHIOATE
Torak EC 24
PHOSPHORODITHIOIC ACID, S-(2-CHLORO-1-(1,3-DIHYDRO-1,3-DIOXO-2H-ISOINDOL-2-YL) ETHYL) O,O-DIETHYL ESTER
PHOSPHORODITHIOIC ACID, S-[2-CHLORO-1-(1,3-DIHYDRO-1,3-DIOXO-2H-ISOINDOL-2-YL) ETHYL] O,O-DIETHYL ESTER
Hercules 14 503
O,O-diethyl S-(2-chloro-1-phthalimidoethyl) phosphorodithioate
USEPA/OPP Pesticide Code: 102501
O,ODiaethylS2chlor1(phthalimido)aethyldithiophosphat
S(2Chloro1phthalmidoethyl)O,Odiethylphosphorothionate
N(2Chloro1(diethoxyphosphinothioylthio)ethyl)phthalimide
O,ODiethyl S(2chloro1phthalimidoethyl)phosphorodithioate
S(2Chloro1phthalimidoethyl) O,Odiethyl phosphorodithioate
S-2-chloro-1-phthalimidoethyl O,O-diethyl phosphorodithioate
Phosphorodithioic acid, S(2chloro1phthalimidoethyl) O,Odiethyl ester
Phosphorodithioic acid, S(2chloro1phthalimidoethyl)O,Odiethyl ester
O,ODiethyl phosphorodithioate Sester with N(2chloro1mercaptoethyl) phthalimide
O,ODiethyl phosphorodithioate Sester with N(2chloro1mercaptoethyl)phthalimide
Phosphorodithioic acid, O,Odiethyl ester, Sester with N(2chloro1mercaptoethyl)phthalimide
Phosphorodithioic acid, S(2chloro1(1,3dihydro1,3dioxo2Hisoindol2yl)ethyl) O,Odiethyl ester
S(2Chloro1(1,3dihydro1,3dioxo2Hisoindol2yl)ethyl) O,Odiethyl phosphorodithioate
S(2Chloro1(1,3dihydro1,3dioxo2Hisoindol2yl)ethyl) O,Odiethyl phosphorodithioate (9CI)
S(2Chloro1(1,3dihydro1,3dioxo2Hisoindol2yl)ethyl)O,Odiethyl phosphorodithioate
Phosphorodithioic acid 5-(2-chloro-1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl) ethyl) O,O-diethyl ester
Phosphorodithioic acid O,O-diethyl ester S-ester with N-(2-chloro-1-mercaptoethyl)phthalimide
Phosphorodithioic acid S-(2-chloro-1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl) ethyl) O,O-diethyl ester
S-(2-Chloro-1-(1,3-dihydro-1,3-dioxy-2H-isoindol-2-yl)ethyl)O,O-diethyl phosphorodithioate
mumqyxacquzofp-uhfffaoysa-n
Dialiphos
Torak
Dialiphor
Hercules 14503
ENT 27320
S-(2-Chloro-1-phthalimidoethyl) O,O-diethyl phosphorodithioate
2-(2-chloro-1-diethoxyphosphinothioylsulfanylethyl)isoindole-1,3-dione
Phosphorodithioic acid, O,O-diethyl ester, S-ester with N-(2-chloro-1-mercaptoethyl)phthalimide
N-(2-Chloro-1-(diethoxyphosphinothioylthio)ethyl)phthalimide
S-(2-Chloro-1-phthalmidoethyl)-O,O-diethylphosphorothionate
CHEBI:82158
Phosphorodithioic acid, S-(2-chloro-1-phthalimidoethyl) O,O-diethyl ester
S-(2-Chloro-1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl)O,O-diethyl phosphorodithioate
O,O-Diaethyl-S-2-chlor-1-(phthalimido)-aethyl-dithiophosphat
Phosphorodithioic acid, S-(2-chloro-1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl) O,O-diethyl ester
Phosphorodithioic acid, S-[2-chloro-1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl] O,O-diethyl ester
O,O-Diaethyl-S-2-chlor-1-(phthalimido)-aethyl-dithiophosphat [German]
Phosphorodithioic acid, S-(2-chloro-1-phthalimidoethyl)-O,O-diethyl ester
O,O-Diethyl phosphorodithioate S-ester with N-(2-chloro-1-mercaptoethyl) phthalimide
O,O-Diethyl phosphorodithioate S-ester with N-(2-chloro-1-mercaptoethyl)phthalimide
SCHEMBL122099
CHEMBL1901826
Tox21_300794
Dialifos 10 microg/mL in Cyclohexane
MSK20128-100M
S-(2-Chloro-1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl) O,O-diethyl phosphorodithioate
NCGC00160634-01
NCGC00160634-02
NCGC00160634-03
NCGC00254698-01
Dialifos Solution in Methanol, 100_g/mL
CAS-10311-84-9
DB-040418
Dialifos, PESTANAL(R), analytical standard
NS00005664
C19028
Q5270555
O,O-DIETHYL S-(2-CHLORO-1- PHTHALIMIDOETHYL)PHOSPHORODITHIOATE
O,O-DIETHYL PHOSPHORODITHIOATE S-ESTER WITH N-(2-CHLORO-1- MERCAPTOETHYL)PHTHALIMIDE
PHOSPHORODITHIOIC ACID, S-(2-CHLORO-1-PHTHALIMIDOETHYL) O,O- DIETHYL ESTER
PHOSPHORODITHIOIC ACID, S-(2-CHLORO-1-PHTHALIMIDOETHYL)-O,O- DIETHYL ESTER
O,O-DIETHYL PHOSPHORODITHIOATE S-ESTER WITH N-(2-CHLORO-1- MERCAPTOETHYL) PHTHALIMIDE
Phosphorodithioic Acid S-[2-chloro-1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl] O,O-diethyl ester
PHOSPHORODITHIOIC ACID, O,O-DIETHYL ESTER, S-ESTER WITH N- (2-CHLORO-1-MERCAPTOETHYL)PHTHALIMIDE
PHOSPHORODITHIOIC ACID, S-(2-CHLORO-1-(1,3-DIHYDRO-1,3- DIOXO-2H-ISOINDOL-2-YL)ETHYL) O,O-DIETHYL ESTER
S-(2-CHLORO-1-(1,3-DIHYDRO-1,3-DIOXO-2H-ISOINDOL-2- YL)ETHYL) O,O-DIETHYL PHOSPHORODITHIOATE
S-[2-Chloro-1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl] O,O-diethyl dithiophosphate #