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(2,5-Dichloro-4-iodophenoxy)dimethoxythiophosphoryl chloride

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Identification
Molecular formula
C8H7Cl2IO3PS
CAS number
87140-73-4
IUPAC name
(2,5-dichloro-4-iodo-phenoxy)-dimethoxy-thioxo-lambda5-phosphane
State
State
Liquid at room temperature.
Melting point (Celsius)
45.00
Melting point (Kelvin)
318.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
425.31g/mol
Molar mass
425.3110g/mol
Density
2.1212g/cm3
Appearence

(2,5-Dichloro-4-iodophenoxy)dimethoxythiophosphoryl chloride typically appears as a colorless to light yellow liquid. Its appearance might vary slightly depending on its purity and the presence of impurities.

Comment on solubility

Solubility of (2,5-dichloro-4-iodo-phenoxy)-dimethoxy-thioxo-lambda5-phosphane

The solubility of (2,5-dichloro-4-iodo-phenoxy)-dimethoxy-thioxo-lambda5-phosphane can be characterized by several key factors, which include its chemical structure, polarity, and interactions with various solvents.

  • Polarity: This compound features both polar and non-polar groups. The presence of the thioxo (S=O) and phenoxy (C6H4O) moieties tends to enhance its solubility in polar solvents, while the chlorinated and iodinated groups may affect its overall polarity.
  • Solvent Compatibility: It is likely to be more soluble in organic solvents such as ethanol, methanol, or acetone. However, due to its complex structure, it may have limited solubility in water, which typically favors more ionic and less hydrophobic substances.
  • Temperature Effects: As with many chemical compounds, solubility can be temperature dependent. Increased temperatures may enhance solubility, particularly in organic solvents.
  • Concentration Effects: Higher concentrations may lead to the formation of aggregates, thus affecting the observed solubility.

In conclusion, while (2,5-dichloro-4-iodo-phenoxy)-dimethoxy-thioxo-lambda5-phosphane is expected to exhibit variable solubility based on the aforementioned factors, further experimental data would be essential to clarify its solubility characteristics. Always refer to experimental conditions when assessing specific solubility results.

Interesting facts

Interesting Facts about (2,5-Dichloro-4-iodo-phenoxy)-dimethoxy-thioxo-lambda5-phosphane

(2,5-Dichloro-4-iodo-phenoxy)-dimethoxy-thioxo-lambda5-phosphane is a unique compound that holds intrigue in both the fields of organic chemistry and materials science. The complexity of its structure makes it a point of interest for researchers exploring novel applications. Here are some fascinating points to consider:

  • Halogen Influence: The presence of chlorine and iodine atoms in the molecule significantly impacts its reactivity and stability. These halogens can enhance biological activity, making this compound a promising candidate for pharmaceutical development.
  • Thioxo Group: The thioxo component, characterized by the sulfur-oxygen double bond, contributes to the unique properties of this phosphane compound. This functional group can influence both the electronic and steric properties, which are critical for understanding reactivity.
  • Organophosphorus Chemistry: As a member of the organophosphorus family, this compound opens avenues for the synthesis of various derivatives. The phosphane framework is essential in ligands for coordination chemistry, catalysis, and even as intermediates in organic synthesis.

Biochemical Potential

Due to the intricate interplay between its various functional groups, this compound may also exhibit interesting biochemical properties. Research in this area could yield:

  • Novel therapeutic agents capable of targeting specific biological pathways.
  • Compounds with inhibitory effects on enzymes relevant to disease mechanisms.
  • Materials designed for drug delivery systems that leverage the reactivity of the thioxo and halogen substituents.

As a final note, the potential applications of (2,5-Dichloro-4-iodo-phenoxy)-dimethoxy-thioxo-lambda5-phosphane in various fields highlight the endless possibilities that lie within the realm of chemistry. The synthesis and study of such complex compounds are crucial for advancements in both theoretical and applied sciences, ultimately transforming our understanding of chemical interactions.

Synonyms
IODOFENPHOS
Jodfenphos
18181-70-9
Alfacron
Iodofenfos
Iodenphos
Iodophos
Trix
Nuvanol N
Iodophenphos
Monocron 9491
O-(2,5-Dichloro-4-iodophenyl) O,O-dimethyl phosphorothioate
ENT 27408
NSC 190998
C 9491
SME6G1846X
DTXSID8040278
O,O-Dimethyl-O-2,5-dichloro-4-iodophenyl thiophosphate
NSC-190998
O,O-Dimethyl-O-(2,5-dichlor-4-jodphenyl)-monothiophosphat
DTXCID6020278
phosphorothioic acid O-(2,5-dichloro-4-iodophenyl) O,O-dimethyl ester
O,O-dimethyl-O-(2,5-dichloro-4-iodophenyl)thiophosphate
242-069-1
Compound C-9491
Ciba-Geigy C-9491
Phosphorothioic acid, O-(2,5-dichloro-4-iodophenyl) O,O-dimethyl ester
CHEBI:82136
Iodofenphos 1000 microg/mL in Acetone
O,O-Dimethyl-O-(2,5-dichlor-4-jodphenyl)-thionophosphat
Iodofenphos 100 microg/mL in Cyclohexane
Jodfenphos [ISO]
Iodofenphos [BAN]
Caswell No. 309B
Ciba C-9491
HSDB 1568
OMS-1211
Iodofenphos [BSI:ISO]
EINECS 242-069-1
EPA Pesticide Chemical Code 309700
BRN 1885795
UNII-SME6G1846X
Iodfenphos
Iodofenophos
Elocril
AI3-27408
C-9491
O-(2,5-Dichloro-4-iodophenyl)-O,O-dimethyl phosphorothioate
IODOFENPHOS [MI]
O,O-Dimethyl-O-(2,5-dichlor-4-jodphenyl)-thionophosphat [German]
O,O-Dimethyl-O-(2,5-dichlor-4-jodphenyl)-monothiophosphat [German]
Phenol, 3,4-dichloro-, O-ester with O-methyl methylphosphoramidothioate
IODOFENPHOS [HSDB]
Ciba 9491
IODOFENPHOS [MART.]
SCHEMBL39677
orb1703356
CHEMBL2106359
CIBA C 9491
MSK20136
OMS 1211
Tox21_300910
(2,5-dichloro-4-iodophenoxy)-dimethoxy-sulfanylidene-lambda5-phosphane
AKOS015903240
NCGC00248206-01
NCGC00254814-01
CAS-18181-70-9
HY-119381
CS-0068025
NS00009634
Jodfenphos, PESTANAL(R), analytical standard
C19002
SR-01000883722
SR-01000883722-1
Q27155764
O,O-Dimethyl O-(2,5-dichloro-4-iodophenyl) phosphorothioate
O-(2,5-Dichloro-4-iodophenyl) O,O-dimethyl thiophosphate #
(2,5-dichloro-4-iodophenoxy)-dimethoxy-sulfanylidene-|E5-phosphane