Skip to main content

N-benzyl-1-ethylsulfanyl-methanimidothioic acid

ADVERTISEMENT
Identification
Molecular formula
C11H15NS2
CAS number
52829-07-9
IUPAC name
N-benzyl-1-ethylsulfanyl-methanimidothioic acid
State
State

At room temperature, N-benzyl-1-ethylsulfanyl-methanimidothioic acid is generally in a solid state, often described as a powdery substance. It's stable under normal conditions of use and storage, provided it's kept dry and away from excessive heat.

Melting point (Celsius)
68.00
Melting point (Kelvin)
341.15
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
243.37g/mol
Molar mass
243.3680g/mol
Density
1.1200g/cm3
Appearence

N-benzyl-1-ethylsulfanyl-methanimidothioic acid typically appears as a pale yellow to light brown solid or powder. Its exact appearance can vary slightly depending on the purity and the specific conditions under which it was prepared and stored.

Comment on solubility

Solubility of N-benzyl-1-ethylsulfanyl-methanimidothioic acid

N-benzyl-1-ethylsulfanyl-methanimidothioic acid, characterized by its unique functional groups, presents interesting solubility properties that are worthy of discussion. The solubility of this compound can be influenced by various factors such as:

  • Polarity: The presence of both polar and non-polar groups may enhance its solubility in a range of solvents.
  • Hydrogen Bonding: The potential for hydrogen bonding due to the imido and thiol functionalities can contribute to solubility in polar solvents.
  • Solvent Effects: N-benzyl-1-ethylsulfanyl-methanimidothioic acid may exhibit better solubility in organic solvents compared to aqueous solutions.

In general, compounds like this can display varied solubility depending on the specific conditions under which they are tested. For instance:

  • It's hypothesized that N-benzyl-1-ethylsulfanyl-methanimidothioic acid might be soluble in organic solvents such as ethanol and dimethyl sulfoxide (DMSO).
  • However, it may show limited solubility in water due to its complex structure.

In conclusion, while comprehensive solubility data may be lacking, understanding the underlying chemical interactions can provide insights into predicting its behavior in different solvents. As always in chemistry, experiment is essential to unveil the true solubility profile of such compounds.

Interesting facts

Interesting Facts about N-benzyl-1-ethylsulfanyl-methanimidothioic acid

N-benzyl-1-ethylsulfanyl-methanimidothioic acid is a fascinating compound that showcases the rich complexity of organic chemistry. This compound is classified as a thioacid, which means it contains a sulfur atom in its functional group, adding unique properties to its chemical behavior. Here are some interesting aspects of this compound:

  • Functional Groups: The presence of both a thioamide and a thiol functional group makes this compound a versatile molecule that can undergo various chemical reactions.
  • Biological Relevance: Compounds with sulfur-containing functional groups are often found in natural products and can exhibit significant biological activity. This raises questions about the potential therapeutic applications of N-benzyl-1-ethylsulfanyl-methanimidothioic acid.
  • Synthetic Pathways: The synthesis of this compound involves several steps that highlight the ingenuity of organic synthesis. Understanding these pathways can provide insights into designing more efficient chemical processes.
  • Applications in Chemistry: Due to its unique structural features, N-benzyl-1-ethylsulfanyl-methanimidothioic acid can serve as an important intermediate in the synthesis of more complex organic molecules.
  • Research Opportunities: The study of this compound opens up potential research avenues, particularly in fields like medicinal chemistry and materials science.

As a student or professional in the field, exploring compounds like N-benzyl-1-ethylsulfanyl-methanimidothioic acid can lead to deeper knowledge of chemical interactions and innovative applications. Consider how the interplay of sulfur in organic compounds can challenge or reshape conventional chemical paradigms!