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Fosthiazate

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Identification
Molecular formula
C9H18ClNO4PS2
CAS number
98886-44-3
IUPAC name
(4-chlorophenyl)sulfanylmethylsulfanyl-dimethoxy-thioxo-lambda5-phosphane
State
State

At room temperature, fosthiazate is in a liquid state due to its relatively low melting point of 10°C. It is important to handle it under controlled conditions due to its volatile nature and particular odor.

Melting point (Celsius)
10.00
Melting point (Kelvin)
283.15
Boiling point (Celsius)
420.30
Boiling point (Kelvin)
693.50
General information
Molecular weight
314.83g/mol
Molar mass
314.8260g/mol
Density
1.2810g/cm3
Appearence

Fosthiazate is typically found as a colorless or pale yellow liquid. It has a characteristic, sharp sulfurous odor, which is common among organophosphorus compounds.

Comment on solubility

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

The solubility of (4-chlorophenyl)sulfanylmethylsulfanyl-dimethoxy-thioxo-lambda5-phosphane can be somewhat intricate due to its complex molecular structure. Understanding the solubility characteristics of this compound encompasses several factors:

  • Polarity: The presence of polar functional groups, such as the thioxo and dimethoxy groups, suggests potential solubility in polar solvents. Conversely, the nonpolar aromatic component might limit its solubility in purely polar environments.
  • Solvent Compatibility: Common solvents that could dissolve this compound might include:
    • Dimethyl sulfoxide (DMSO)
    • Acetonitrile
    • Alcohols such as methanol or ethanol
  • Temperature Effects: Increased temperature may improve solubility, as it typically enhances the dissolution process by increasing molecular motion and breaking intermolecular interactions.

As noted, the solubility of this compound can be significantly affected by its unique chemical structure. It is essential to perform empirical solubility tests under varying conditions to gain a complete understanding of its solubility profile.

Interesting facts

Interesting Facts about (4-Chlorophenyl)sulfanylmethylsulfanyl-dimethoxy-thioxo-lambda5-phosphane

(4-Chlorophenyl)sulfanylmethylsulfanyl-dimethoxy-thioxo-lambda5-phosphane is a fascinating compound that belongs to the class of organophosphorus compounds. Here are some intriguing points about it:

  • Organophosphorus Chemistry: This compound is part of a broader domain of organic chemistry where phosphorus is a central atom. Organophosphorus compounds are essential due to their various industrial and agricultural applications.
  • Biological Activity: Compounds containing phosphorus often exhibit biological activity, making them crucial in the development of pesticides and pharmaceuticals. They can interact with biological systems in significant ways.
  • Functional Groups: The presence of multiple functional groups, such as the chlorophenyl, sulfanyl, and dimethoxy groups, lends this compound its unique properties and potential utility in organic synthesis.
  • Thio and Methoxy Groups: These groups can influence the reactivity of the compound, offering pathways for further reactions, and enhancing solubility in various solvents.
  • Research Significance: Compounds like this are often the focus of research aiming to develop new drugs or agrochemicals due to their multifaceted capabilities.

An important aspect to note is that while compounds of this nature can be incredibly useful, they also require careful handling and study. Understanding their full potential can lead to groundbreaking advancements in both chemistry and applied sciences.

As a chemistry student or professional, diving deep into the properties and applications of such compounds opens up a world of discoveries awaiting exploration!

Synonyms
METHYL TRITHION
Carbophenothion-methyl
Methyl Carbophenothion
953-17-3
Carbophenothion methyl
Trithion-methyl
Tri-Me
Geigy G-29288
Methyltrithion
Methylcarbophenothion
Stauffer R-1492
Caswell No. 212
ENT 25,599
Stauffer R 1492
ENT 25586
NSC 231692
HSDB 1545
O,O-Dimethylthiophosphoric acid p-chlorophenyl ester
UNII-X08H286BAN
EPA Pesticide Chemical Code 058101
BRN 2506804
X08H286BAN
G-29288
AI3-25586
Dimethyl p-chlorophenylthiomethyl dithiophosphate
S-(((4-Chlorophenyl)thio)methyl) O,O-dimethylphosphorodithioate
NSC-231692
Phosphorodithioic acid, S-(((4-chlorophenyl)thio)methyl) O,O-dimethyl ester
Methanethiol, ((p-chlorophenyl)thio)-, S-ester with O,O-dimethyl phosphorodithioate
METHYL TRITHION [HSDB]
O,O-Dimethyl-S-(p-chlorophenylthiomethyl)phosphorodithioate
DTXSID3040275
S-(((p-Chlorophenyl)thio)methyl) O,O-dimethyl phosphorodithioate
Phosphorodithioic acid, S-(((p-chlorophenyl)thio)methyl) O,O-dimethyl ester
Phosphorodithioic acid, S-[[(4-chlorophenyl)thio]methyl] O,O-dimethyl ester
S-[[(p-Chlorophenyl)thio]methyl] O,O-dimethyl phosphorodithioate
Phosphorodithioic acid, S-[[(p-chlorophenyl)thio]methyl] O,O-dimethyl ester
Dimethyl (((p-chlorophenyl)thio)methyl) dithiophosphate
O,O-Dimethyl-S-(((p-chlorophenyl)thio)methyl)phosphorodithioate
Dimethyl [[(p-chlorophenyl)thio]methyl] dithiophosphate
Trithionmethyl
O,O-Dimethyl-S-[[(p-chlorophenyl)thio]methyl]phosphorodithioate
TriMe
Carbophenothionmethyl
Stauffer R1492
Geigy G29288
DTXCID1020275
Dimethyl pchlorophenylthiomethyl dithiophosphate
O,ODimethylS(pchlorophenylthiomethyl)phosphorodithioate
S(((4Chlorophenyl)thio)methyl) O,Odimethylphosphorodithioate
S(((pChlorophenyl)thio)methyl) O,Odimethyl phosphorodithioate
Phosphorodithioic acid, S(((4chlorophenyl)thio)methyl) O,Odimethyl ester
Phosphorodithioic acid, S(((pchlorophenyl)thio)methyl) O,Odimethyl ester
Methanethiol, ((pchlorophenyl)thio), Sester with O,Odimethyl phosphorodithioate
Phosphorodithioic acid, S-(((4-chlorophenyl)thio)methyl) O,O-dimethyl ester (9CI)
4-06-00-01595 (beilstein handbook reference)
g29288
ouccvxvygfbxsv-uhfffaoysa-n
r-1492
Methyl Trithion (Technical Grade)
(4-chlorophenyl)sulfanylmethylsulfanyl-dimethoxy-sulfanylidene-lambda5-phosphane
Phosphorodithioic acid, S-[[(4-chlorophenyl)thio]methyl] O,O-dimethylester
Carbophenothion-methyl 100 microg/mL in Acetonitrile
SCHEMBL5933780
WLN: GR DS1SPS&O1&O1
NSC231692
Phosphorodithioic acid,O-dimethyl ester
1ST20534
NS00073925
Q27293162
Methanethiol, S-ester with O,O-dimethyl phosphorodithioate
S-([(4-Chlorophenyl)sulfanyl]methyl) O,O-dimethyl dithiophosphate #