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N-allyl-1-ethoxy-methanimidothioic acid

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Identification
Molecular formula
C7H13NOS
CAS number
4012-47-1
IUPAC name
N-allyl-1-ethoxy-methanimidothioic acid
State
State

This compound is commonly found as a liquid at room temperature, maintaining its state under typical atmospheric conditions. It is not solidified in standard room temperature environments and remains stable as a liquid.

Melting point (Celsius)
-35.00
Melting point (Kelvin)
238.15
Boiling point (Celsius)
212.00
Boiling point (Kelvin)
485.15
General information
Molecular weight
159.25g/mol
Molar mass
159.2450g/mol
Density
1.0200g/cm3
Appearence

N-allyl-1-ethoxy-methanimidothioic acid presents as a colorless liquid. Its appearance is characterized by a clear, transparent liquid form that is typically mobile and exhibits typical liquid behavior in terms of fluidity.

Comment on solubility

Solubility of N-allyl-1-ethoxy-methanimidothioic acid

N-allyl-1-ethoxy-methanimidothioic acid, with its unique structure and functional groups, presents interesting characteristics regarding its solubility. Let’s break down some key points:

  • Polar Functional Groups: The presence of the thioic acid and ethoxy groups suggests that this compound could exhibit significant polarity, which typically enhances its solubility in polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds may further impact solubility. Compounds capable of hydrogen bonding often demonstrate high solubility in water.
  • Nature of Solvents: N-allyl-1-ethoxy-methanimidothioic acid is likely soluble in various organic solvents such as alcohols and ethers but may have limited solubility in non-polar solvents.
  • Temperature Dependence: Solubility can be highly sensitive to temperature; thus, elevated temperatures might enhance the solubility of this compound in certain solvents.

Overall, while specific solubility data for N-allyl-1-ethoxy-methanimidothioic acid may not be widely documented, one can infer from its chemical structure that it is likely to be more soluble in polar solvents. This makes it valuable for applications requiring solubilization in aqueous or polar organic media.

Interesting facts

Interesting Facts About N-allyl-1-ethoxy-methanimidothioic Acid

N-allyl-1-ethoxy-methanimidothioic acid, a member of the thioamide family, is a fascinating compound that showcases the unique properties and behaviors of thiocarbonyl-containing substances. Here are some intriguing aspects of this compound:

  • Application in Agriculture: This compound may play a role in agricultural chemistry, particularly as a potential agrochemical due to its thioamide functional group, which is often associated with biological activity.
  • Thioamide Chemistry: Thioamides are known for their ability to participate in a variety of chemical reactions, including nucleophilic substitution and condensation, making N-allyl-1-ethoxy-methanimidothioic acid a versatile molecule in synthetic chemistry.
  • Biological Activity: Some thioamide compounds exhibit antimicrobial and herbicidal properties, which indicates that the interactions of this compound might be worth exploring for its potential in developing new agricultural agents.
  • Role in Synthesis: This compound might serve as a key intermediate in the synthesis of more complex molecules, providing opportunities for chemists to enhance yields and streamline synthetic pathways.

The study of such compounds illuminates the complex interplay between structure and reactivity in organic chemistry. As one might say, "The beauty of chemistry lies in its ability to connect the dots between seemingly disparate molecular systems." Exploring compounds like N-allyl-1-ethoxy-methanimidothioic acid not only broadens our understanding of thioamide chemistry but also expands the toolkit available for chemists seeking new applications in various industries.