Skip to main content

Tetrathiooxalate

ADVERTISEMENT
Identification
Molecular formula
C2S42−
CAS number
2642-56-2
IUPAC name
2-[carboxymethylsulfanyl-(4-ureidophenyl)arsanyl]sulfanylacetic acid
State
State

At room temperature, tetrathiooxalate is a solid compound, often encountered in its sodium salt form.

Melting point (Celsius)
258.00
Melting point (Kelvin)
531.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
270.08g/mol
Molar mass
270.0800g/mol
Density
2.1680g/cm3
Appearence

Tetrathiooxalate typically presents as a white crystalline powder. It is often used in its sodium salt form, which also appears as a white solid.

Comment on solubility

Solubility of 2-[carboxymethylsulfanyl-(4-ureidophenyl)arsanyl]sulfanylacetic acid

The solubility of 2-[carboxymethylsulfanyl-(4-ureidophenyl)arsanyl]sulfanylacetic acid can be influenced by a variety of factors due to its complex structure. Here are a few key points to consider:

  • Water Solubility: Given the presence of carboxymethyl and sulfanyl groups, this compound is likely to exhibit moderate to high solubility in water, benefiting from ionic interactions and hydrogen bonding.
  • Polar Solvents: It may demonstrate good solubility in polar organic solvents such as ethanol and methanol, where its polar functional groups can interact favorably.
  • Non-Polar Solvents: Conversely, solubility in non-polar solvents could be quite limited due to its polar character, making it less soluble in environments that lack polar interactions.
  • Temperature Dependence: As with many organic compounds, increasing temperature may enhance solubility, which could influence its behavior in various applications.

In summary, the solubility of 2-[carboxymethylsulfanyl-(4-ureidophenyl)arsanyl]sulfanylacetic acid is likely to reflect a strong dependence on the solvent properties, especially in regard to polarity. Therefore, one could say that the statement—"the solubility is contingent on the chemical environment"—holds true for this compound.

Interesting facts

Interesting Facts about 2-[carboxymethylsulfanyl-(4-ureidophenyl)arsanyl]sulfanylacetic acid

This fascinating compound features a unique combination of functional groups that contribute to its properties and potential applications. Here are some key points that highlight its significance:

  • Dual Functionalities: The presence of both sulfanyl and carboxymethyl groups allows this compound to exhibit unique reactivity and interactions that can be exploited in various chemical reactions.
  • Metal Complexation: Due to the arsanyl group within its structure, this compound has a strong potential for forming coordination complexes with metal ions, which may enhance its application in catalysis and materials science.
  • Pharmaceutical Potential: As a derivative of aromatic amines, it is structurally related to many pharmacologically active compounds. Researchers are investigating its potential use in medicinal chemistry, particularly in drug development.
  • Research Impact: The compound is part of a larger class of organosulfur compounds, which have been widely studied for their biological activities, including anticancer, antimicrobial, and antioxidant effects.

As a scientist or chemistry student, you might find it intriguing that the synthesis and characterization of this compound merge classic organic chemistry techniques with modern analytical methods. The study of such compounds not only broadens our understanding of chemical interactions but also opens doors to new innovations in various fields.

In conclusion, 2-[carboxymethylsulfanyl-(4-ureidophenyl)arsanyl]sulfanylacetic acid stands as a testament to the intricate connections between structure and function in chemistry, showcasing how diverse chemical identities can lead to exciting possibilities.

Synonyms
Thiocarbarsone
120-02-5
C.C. No. 914
Chemotherapy Center No. 914
UNII-5ZBS38PFRD
5ZBS38PFRD
CC 914
4-Carbamidophenyl bis(carboxymethylthio)arsenite
Bis(carboxymethylmercapto)(p-ureidophenyl)arsine
2-[[4-(carbamoylamino)phenyl]-(carboxymethylsulfanyl)arsanyl]sulfanylacetic acid
(p-Ureidophenylarsylenedithio)diacetic acid
Phenyl urea p-di(carboxymethyl) thioarsenite
Arsine, bis(carboxymethylthio)(p-ureidophenyl)-
THIOCARBARSONE [MI]
Acetic acid, (p-carbamoylamino)phenylarsinobis(2-thio-
DTXSID40152638
Mercaptoacetic acid, diester with dithio-p-ureidobenzenearsonous acid
Benzenearsonous acid, dithio-p-ureido-, diester with mercaptoacetic acid
Acetic acid, 2,2'-((4-((aminocarbonyl)amino)phenyl)arsinidene)bis(thio)bis-
ACETIC ACID, MERCAPTO-, DIESTER with DITHIO-p-UREIDOBENZENEARSONOUS ACID
Bis[carboxymethylmercapto](p-ureidophenyl)arsine; CC 914
2-[[4-(carbamoylamino)phenyl]-(carboxymethylsulfanyl)arsanyl]sulfanyla cetic acid
SCHEMBL672661
DTXCID3075129
DB-251091
Q27263099