Skip to main content

Thiourea

ADVERTISEMENT
Identification
Molecular formula
CH4N2S
CAS number
62-56-6
IUPAC name
2-carbamimidoylsulfanylisothiourea
State
State

At room temperature, thiourea is typically a solid.

Melting point (Celsius)
182.00
Melting point (Kelvin)
455.15
Boiling point (Celsius)
150.00
Boiling point (Kelvin)
423.00
General information
Molecular weight
76.12g/mol
Molar mass
76.1220g/mol
Density
1.4050g/cm3
Appearence

Thiourea is a colorless and crystalline solid. It is similar in appearance and texture to granular white sugar.

Comment on solubility

Solubility of 2-Carbamimidoylsulfanylisothiourea

The solubility of 2-carbamimidoylsulfanylisothiourea in various solvents is a critical aspect to consider when evaluating its potential applications in chemical processes or biological systems. This compound exhibits distinctive solubility characteristics:

  • Aqueous Solubility: 2-carbamimidoylsulfanylisothiourea tends to show moderate solubility in water due to its polar functional groups, making it useful for reactions requiring aqueous phases.
  • Solubility in Organic Solvents: The solubility in organic solvents like methanol or ethanol may vary; typically, it's less soluble than in water, which can be influenced by the presence of functional groups.
  • Influence of pH: The solubility can also be affected by pH levels, with enhanced solubility in more alkaline or acidic conditions which can stabilize ionic forms of the compound.

Moreover, it is important to note:

  • Specific interactions with solvents can lead to hydrogen bonding, impacting overall solubility.
  • Temperature variations can also change solubility profiles, with higher temperatures generally increasing solubility for many compounds.

In conclusion, understanding the solubility of 2-carbamimidoylsulfanylisothiourea is essential not only for its practical applications but also for predicting its behavior in chemical reactions. As with many compounds, testing in specific conditions may yield more accurate solubility data.

Interesting facts

Interesting Facts about 2-Carbamimidoylsulfanylisothiourea

The compound 2-carbamimidoylsulfanylisothiourea, often abbreviated in scientific contexts, presents a fascinating profile in the realm of chemical compounds. Here are several engaging and noteworthy points about this intriguing molecule:

  • Unique Structure: This compound features a distinctive arrangement that includes both isothiourea and sulfanylimine functional groups, leading to diverse reactivity and interactions.
  • Biological Relevance: Compounds like this one are frequently investigated for their potential biological activities, including antiviral and antibacterial properties, highlighting the intersection of chemistry and medicine.
  • Research Applications: Its structural characteristics make it a candidate for further research in the development of novel pharmaceuticals, particularly in the field of drug design.
  • Versatile Functionality: The presence of the carbamimidoyl and thiourea groups contributes to a wide variety of chemical reactions, making this compound a valuable tool for synthetic chemists.
  • Academic Interest: Chemistry students and researchers often study such compounds not only for their intrinsic properties but also for their implications in understanding more complex systems.

As noted by one prominent chemist, "The study of compounds like 2-carbamimidoylsulfanylisothiourea not only expands our chemical vocabulary but also deepens our understanding of molecular interactions and their biological significance." This encapsulates the essence of why such compounds are pivotal in both academic and practical applications.

In conclusion, 2-carbamimidoylsulfanylisothiourea serves as a remarkable example of how seemingly simple structures can hold extraordinary capabilities and open new avenues of research.

Synonyms
Disulfidodicarbamidine
3256-06-2
AD3N79Q9D5
formamidine disulfide
DTXSID90186261
NSC-677543 FREE BASE
Thioperoxydicarbonimidic diamide (((H2N)C(NH))2S2)
DTXCID00108752
carbamimidoylsulfanyl carbamimidothioate
NSC677543
NSC-677543
Formamidindisulfid
formamidine disulphide
UNII-AD3N79Q9D5
SCHEMBL676868
Disulfanyl-1,2-dicarboxamidine
CHEMBL120477
2-carbamimidoylsulfanylisothiourea
GJLUFTKZCBBYMV-UHFFFAOYSA-N
AKOS015833395
NS00121626