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2-[(2-carboxyphenyl)sulfanyl-(4-ureidophenyl)arsanyl]sulfanylbenzoic acid

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Identification
Molecular formula
C20H16AsN2O4S2
CAS number
114-04-5
IUPAC name
2-[(2-carboxyphenyl)sulfanyl-(4-ureidophenyl)arsanyl]sulfanylbenzoic acid
State
State

At room temperature, it exists as a solid. It maintains stability under standard conditions and should be handled with care in well-ventilated areas.

Melting point (Celsius)
168.00
Melting point (Kelvin)
441.15
Boiling point (Celsius)
465.00
Boiling point (Kelvin)
738.15
General information
Molecular weight
469.55g/mol
Molar mass
469.5450g/mol
Density
1.4200g/cm3
Appearence

The compound is typically characterized as a solid with a crystalline structure. The appearance can range from off-white to light tan powder depending on impurities and form.

Comment on solubility

Solubility of 2-[(2-carboxyphenyl)sulfanyl-(4-ureidophenyl)arsanyl]sulfanylbenzoic acid

This intriguing compound, with its multifaceted chemical structure, presents an interesting case for solubility considerations. The solubility of a compound in a given solvent can significantly influence its application and functionality in various fields. Here are some key points regarding the solubility of this compound:

  • Solvent Polarity: The presence of carboxylic acid groups generally enhances solubility in polar solvents, such as water, due to hydrogen bonding capabilities.
  • Functional Groups: The phenyl and sulfanyl groups could introduce both hydrophobic and hydrophilic interactions, impacting the overall solubility profile.
  • Temperature Effects: As with many organic compounds, solubility may increase with temperature, allowing for more efficient dissolution in warm solvents.
  • pH Considerations: Given the carboxylic acid functionality, the solubility may be influenced by the pH of the solution, whereby increased pH may lead to deprotonation and thus higher solubility.

In summary, the solubility of 2-[(2-carboxyphenyl)sulfanyl-(4-ureidophenyl)arsanyl]sulfanylbenzoic acid will likely depend on a combination of these factors. Testing in various solvents will provide a clearer picture of its solubility traits, making it a subject of ongoing interest in chemical research.

Interesting facts

Interesting Facts about 2-[(2-carboxyphenyl)sulfanyl-(4-ureidophenyl)arsanyl]sulfanylbenzoic acid

This complex compound is an intriguing example of organoarsenic chemistry and showcases the unique interplay between sulfur, carbon, and arsenic elements. Here are some noteworthy points to consider:

  • Multifunctional Groups: The compound contains both carboxylic acid and urea functional groups, indicating potential for versatile reactivity. These moieties may allow it to act as a ligand in coordination chemistry or serve as a building block in supramolecular assemblies.
  • Biological Relevance: Compounds containing arsenic can exhibit varying biological activities. Some organoarsenic compounds have been studied for their antitumor activity or involvement in pharmaceuticals. This makes them a focal point of research in medicinal chemistry.
  • Environmental Chemistry: The presence of arsenic raises significant environmental concerns. Its compounds are scrutinized for their toxicity and potential effects on ecosystems. Understanding how compounds like this one interact with natural systems is vital for environmental protection.
  • Synthetic Interest: Creating such specialized compounds may involve advanced synthetic techniques, including cross-coupling reactions or functionalization strategies. This challenges chemists to develop efficient pathways to access compounds with specific functionalities.
  • Research Potential: Given the compound's complex structure, it presents numerous opportunities for research in areas such as catalysis, materials science, and coordination chemistry. Investigating its properties could yield new insights into chemical behavior and applications.

In summary, 2-[(2-carboxyphenyl)sulfanyl-(4-ureidophenyl)arsanyl]sulfanylbenzoic acid is not just a compound of theoretical interest; it embodies practical implications across various scientific fields, making it a compelling subject for further study and exploration.

Synonyms
Thiocarbamizine
Thiocarbamisin
91-71-4
THIO-CARBAMISIN
Chemotherapy Center No. 1037
(p-Ureidophenylarsylenedithio)di-o-benzoic acid
4-Carbamidophenyl bis(o-carboxyphenylthio)arsenite
o-Mercaptobenzoic acid, diester with dithio-p-ureidobenzenearsonous acid
(p-Ureidophenylarsylenedithio)di-o-benioic acid
NSC 523316
(p-Ureidobenzenearsylenedithio)di-o-benzoic acid
UNII-J1180JH294
p-Carbamidophenyl-bis(2-carboxyphenylmercapto)arsine
p-Carbamidophenyl-di(1'-carboxyphenyl-2') thioarsenite
J1180JH294
NSC-523316
p-(Bis(o-carboxyphenylmercapto)-arsino)-phenylurea
THIOCARBAMIZINE [MI]
2-[[4-(carbamoylamino)phenyl]-(2-carboxyphenyl)sulfanylarsanyl]sulfanylbenzoic acid
BENZOIC ACID, o-MERCAPTO-, DIESTER with DITHIO-p-UREIDOBENZENEARSONOUS ACID
NSC 523316; Thiocarbamisin
DTXSID90238355
Benzenearsonous acid, dithio-p-ureido-, diester with o-mercaptobenzoic acid
Benzoic acid, 2,2'-(((4-((aminocarbonyl)amino)phenyl)arsinidene)bis(thio))bis-
Benzoic acid, 2,2'-(((4-((aminocarbonyl)amino)phenyl)arsinidenebis(thio))bis)
Benzoic acid, o-mercapto-, S,S-diester with dithio-p-ureidobenzenearsonous acid
4-Carbamidophenyl bis[o-carboxyphenylthio]arsenite
p-[Bis(o-carboxyphenylmercapto)-arsino]-phenylurea
SCHEMBL672375
C.c. no. 1037
DTXCID10160846
NSC523316
WLN: ZVMR D-AS-SR BOVH& SR BOVH
Q27281007
Benzenearsonous acid, diester with o-mercaptobenzoic acid
Benzoic acid, diester with dithio-p-ureidobenzenearsonous acid
Benzoic acid, S,S-diester with dithio-p-ureidobenzenearsonous acid
Benzoic acid,2'-[[[4-[(aminocarbonyl)amino]phenyl]arsinidenebis(thio)]bis]
2,2'-[[[4-[(AMINOCARBONYL)AMINO]PHENYL]ARSINIDENE]BIS(THIO)]BIS[BENZOIC ACID]
Benzoic acid, 2,2'-(((4-((aminocarbonyl)amino)phenyl)arsinidene)bis(thio))bis-(9CI)
Benzoic acid,2'-[[[4-[(aminocarbonyl)amino]phenyl]arsinidene]bis(thio)]bis-