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S-methyl N-(3-hydroxyphenyl)carbamothioate

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Identification
Molecular formula
C8H9NO2S
CAS number
123-33-1
IUPAC name
S-methyl N-(3-hydroxyphenyl)carbamothioate
State
State

At room temperature, S-methyl N-(3-hydroxyphenyl)carbamothioate is typically found in a solid state.

Melting point (Celsius)
116.00
Melting point (Kelvin)
389.15
Boiling point (Celsius)
269.00
Boiling point (Kelvin)
542.15
General information
Molecular weight
183.24g/mol
Molar mass
183.2420g/mol
Density
1.2900g/cm3
Appearence

This compound is typically a crystalline solid with a distinct odor. It can be colorless to pale yellow in appearance.

Comment on solubility

Solubility of S-methyl N-(3-hydroxyphenyl)carbamothioate

S-methyl N-(3-hydroxyphenyl)carbamothioate, often referred to in the field of chemical research, possesses unique solubility characteristics that are important for its applications. Understanding its solubility can provide valuable insights into its behavior in various solvents:

  • Water Solubility: This compound is generally expected to have low solubility in water due to its hydrophobic carbamate structure.
  • Organic Solvents: It is likely to be more soluble in organic solvents such as:
    • Dimethyl sulfoxide (DMSO)
    • Acetone
    • Ethanol
  • Solvent Interactions: The presence of the 3-hydroxyphenyl group provides potential for hydrogen bonding, which may enhance solubility in polar organic solvents.

In summary, the solubility of S-methyl N-(3-hydroxyphenyl)carbamothioate is influenced by its specific molecular structure, and careful consideration of solvent choice is crucial for its effective use in chemical processes.

Interesting facts

Interesting Facts About S-methyl N-(3-hydroxyphenyl)carbamothioate

S-methyl N-(3-hydroxyphenyl)carbamothioate is a fascinating compound that plays a role in both medicinal and agricultural chemistry. Here are some key points that highlight its significance:

  • Biological Activity: This compound has shown potential as a bioactive molecule, which means it can interact with biological systems in a way that may produce beneficial effects.
  • Pesticide Properties: S-methyl N-(3-hydroxyphenyl)carbamothioate belongs to a class of compounds known for their use in agricultural practices. Some derivatives offer protective properties against pests, making them valuable in crop management.
  • Structure-Activity Relationship: The molecular structure of this compound, with its thioate and hydroxyl functional groups, contributes to its reactivity and interactions with various other chemical species. Chemists often study such relationships to design more effective compounds.
  • Research Applications: Ongoing studies focus on the potential pharmacological applications of this compound, including its effects on specific enzyme pathways. Such research may lead to the discovery of new therapeutic agents.
  • Sustainable Chemistry: As part of the green chemistry movement, research into compounds like S-methyl N-(3-hydroxyphenyl)carbamothioate reflects the aim to develop more environmentally friendly pesticides and pharmaceuticals.

In summary, S-methyl N-(3-hydroxyphenyl)carbamothioate is more than just a chemical formula; it represents the intersection of several scientific fields, including pharmacology, agricultural science, and green chemistry. Its unique properties and potential applications make it an interesting subject for further exploration in the world of chemistry.

Synonyms
19962-05-1
CARBANILIC ACID, m-HYDROXYTHIO-, S-METHYL ESTER
S-methyl N-(3-hydroxyphenyl)carbamothioate
S-Methyl (3-hydroxyphenyl)carbamothioate
S-Methyl m-hydroxythiocarbanilate
m-Hydroxythiocarbanilic acid S-methyl ester
starbld0031726
orb1986290
SCHEMBL11290332
DTXSID10173754
AKOS040751023