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2-Ethoxycarbothioylsulfanylacetic acid

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Identification
Molecular formula
C6H10O3S2
CAS number
7098-76-6
IUPAC name
2-ethoxycarbothioylsulfanylacetic acid
State
State

At room temperature, it is a solid.

Melting point (Celsius)
54.00
Melting point (Kelvin)
327.15
Boiling point (Celsius)
212.00
Boiling point (Kelvin)
485.15
General information
Molecular weight
194.27g/mol
Molar mass
194.2500g/mol
Density
1.2600g/cm3
Appearence

2-Ethoxycarbothioylsulfanylacetic acid is typically a white to off-white powder or crystalline solid.

Comment on solubility

Solubility of 2-ethoxycarbothioylsulfanylacetic acid

The solubility characteristics of 2-ethoxycarbothioylsulfanylacetic acid can provide insights into its potential applications and efficacy in various settings. This compound exhibits some intriguing solubility behavior:

  • Polarity: The presence of both an ethoxy group and a carboxylic acid group hints at a degree of polarity, which generally enhances solubility in polar solvents such as water.
  • Solvent Interaction: This compound is likely to be soluble in organic solvents, such as ethanol and acetone, due to its hydrophobic carbon chain.
  • pH Dependency: The solubility can vary with pH; at lower pH values, the carboxylic group may be protonated, potentially affecting overall solubility.
  • Temperature Effects: Increased temperature is expected to enhance solubility, particularly in organic solvents, by promoting more molecular motion.

As with many compounds, the solubility of 2-ethoxycarbothioylsulfanylacetic acid is influenced by multiple factors. For practical applications, understanding these variables is crucial:

  1. This compound is anticipated to dissolve readily in polar aprotic solvents.
  2. It showcases variable solubility depending on environmental conditions, particularly temperature and pH.
  3. Furthermore, it is essential to consider that the solubility may differ across compositions and concentrations, which could be explored through empirical experimentation.

In conclusion, 2-ethoxycarbothioylsulfanylacetic acid’s solubility profile suggests versatility in practical applications, making it a candidate for further study in pharmaceutical and chemical research.

Interesting facts

Interesting Facts about 2-ethoxycarbothioylsulfanylacetic acid

2-ethoxycarbothioylsulfanylacetic acid is a fascinating compound within the realm of organic chemistry, showcasing the beauty and complexity of sulfur-containing compounds. Here are some intriguing aspects of this unique compound:

  • Functional Groups: This compound contains multiple functional groups, including a carboxylic acid and a thioether, making it a point of interest for those studying functional group reactivity and interactions.
  • Synthesis Potential: Chemists have explored various synthetic routes for obtaining this compound, often employing methods that involve both nucleophilic substitution and condensation reactions.
  • Biological Activity: Compounds with similar structures often exhibit interesting biological properties. Researchers are curious about the potential pharmaceutical applications of 2-ethoxycarbothioylsulfanylacetic acid, particularly in drug design.
  • Reactivity of Sulfur: The presence of sulfur in its structure can lead to unique reactivity patterns, such as the ability to form cyclic compounds or engage in oxidation-reduction reactions.
  • Applications: This compound can serve as a building block in the development of agrochemicals and other specialty chemicals, expanding its relevance in industrial chemistry.

As we continue to uncover the properties and applications of 2-ethoxycarbothioylsulfanylacetic acid, it stands as a testament to the rich diversity and potential found in organic compounds. Scientists are eager to explore its chemistry further, hoping to reveal more about its behavior and potential uses in various fields.

Synonyms
25554-84-1
Carboxymethyl ethylxanthate
Ethyl xanthogeneacetic acid
2-((Ethoxycarbonothioyl)thio)acetic acid
Xanthic acid, ethyl-, carboxymethyl ester
((Ethoxythiomethyl)thio)acetic acid
Xanthic acid, ethyl-, ester with mercaptoacetic acid
NSC 85743
NSC-85743
BRN 1771184
Dithiocarbonic acid S-carboxymethyl O-ethyl ester
H778OG3C6S
Acetic acid, ((ethoxythioxomethyl)thio)-
Acetic acid, [(ethoxythioxomethyl)thio]-
Acetic acid, ((ethoxythiomethyl)thio)-
Carbonic acid, dithio-, O-ethyl ester, S-ester with mercaptoacetic acid
S-(Carboxymethyl) O-ethyl dithiocarbonate
CARBONIC ACID, DITHIO-, S-CARBOXYMETHYL O-ETHYL ESTER
DTXSID60180251
4-03-00-00611 (Beilstein Handbook Reference)
((ETHOXYTHIOCARBONYL)THIO)ACETIC ACID
S-ETHOXYTHIOCARBONYLMERCAPTOACETIC ACID
2-((ETHOXYTHIOXOMETHYL)THIO)ACETIC ACID
ACETIC ACID, 2-((ETHOXYTHIOXOMETHYL)THIO)-
ACETIC ACID, MERCAPTO-, O-ETHYL DITHIOCARBONATE
2-[(Ethoxythioxomethyl)thio]acetic acid
2-[(Ethoxycarbonothioyl)thio]acetic Acid
RefChem:574639
DTXCID70102742
Acetic acid, ((ethoxythiomethyl)thio)-(9CI)
Acetic acid, ((ethoxythioxomethyl)thio)-(9CI)
Carbonic acid, dithio-, O-ethyl ester, S-ester with mercaptoacetic acid (8CI)
623-864-6
[(ethoxycarbonothioyl)thio]acetic acid
2-ethoxycarbothioylsulfanylacetic acid
2-[(ethoxymethanethioyl)sulfanyl]acetic acid
MFCD00022145
C5H8O3S2
NSC85743
2-(ethoxythioxomethylthio)acetic acid
WLN: SUYO2&S1VQ
NCIStruc1_000099
NCIStruc2_000179
UNII-H778OG3C6S
ETHYLXANTHOGENACETIC ACID
SCHEMBL3412115
CHEMBL1446522
ALBB-026263
NCI85743
((ethoxycarbothioyl)thio)acetic acid
CCG-36305
Ethoxythiocarbonylsulfanyl-acetic acid
NCGC00013900
SBB058117
AKOS003684870
S-ethoxythiocarbonyl mercaptoacetic acid
2-((Ethoxycarbonothioyl)thio)aceticacid
5-Oxa-3-thiaheptanoic acid, 4-thioxo-
NCGC00013900-02
NCGC00097009-01
LS-08923
NCI60_041895
SY333948
2-[(Ethoxycarbonothioyl)sulfanyl]acetic acid
Carbonic acid, S-carboxymethyl o-ethyl ester
ST45029642
E87595