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Metolcarb

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Identification
Molecular formula
C8H7NO3S
CAS number
1129-41-5
IUPAC name
S-(4-nitrophenyl) N-methylcarbamothioate
State
State

At room temperature, Metolcarb is found in a solid state.

Melting point (Celsius)
50.00
Melting point (Kelvin)
323.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
214.24g/mol
Molar mass
214.2400g/mol
Density
1.3780g/cm3
Appearence

Metolcarb appears as a crystalline solid which may be colorless or pale yellow. It has a slight odor that can be detected if present in concentrations sufficient or in the air.

Comment on solubility

Solubility of S-(4-nitrophenyl) N-methylcarbamothioate

S-(4-nitrophenyl) N-methylcarbamothioate, characterized by its complex structure, presents interesting properties regarding its solubility profile. The solubility of this compound can be influenced by several factors, making it crucial for various applications:

  • Polarity: The presence of the nitrophenyl group increases the polarity of the molecule, suggesting that it could have better solubility in polar solvents such as water or dimethyl sulfoxide (DMSO).
  • Hydrogen Bonding: The potential for hydrogen bonding due to functional groups plays a significant role; for example, the carbamothioate moiety may interact favorably with polar solvents, enhancing solubility.
  • Solvent Choice: Solubility can vary when using different solvents. For instance, it is likely to be less soluble in nonpolar solvents like hexane, as the nonpolar interactions would not effectively overcome the polar nature of the compound.

Thus, for researchers and practitioners working with S-(4-nitrophenyl) N-methylcarbamothioate, understanding these solubility factors is vital for its effective use in chemical processes and formulations. As with many compounds, the knowledge of solubility not only aids in predicting behavior in various environments but also guides in making informed decisions when selecting solvents for experiments.

Interesting facts

Interesting Facts about S-(4-nitrophenyl) N-methylcarbamothioate

S-(4-nitrophenyl) N-methylcarbamothioate is a fascinating compound within the realm of organosulfur chemistry. Here are some key insights that showcase its unique characteristics and applications:

  • Chemical Structure: This compound features a thiocarbonyl group and a nitrophenyl substituent, making it an interesting subject for studying the reactivity of thioester derivatives.
  • Biological Activity: S-(4-nitrophenyl) N-methylcarbamothioate is noted for its potential biological applications. It may exhibit herbicidal properties, providing a useful tool in agricultural chemistry.
  • Reactivity: Its structure allows for a range of chemical reactions, including nucleophilic substitutions and hydrolysis, which are critical for evaluating its functionality in various synthetic pathways.
  • Environmental Impact: Understanding the degradation and environmental fate of this compound is crucial, especially if it is used in agricultural applications, where the eco-compatibility of herbicides is a major concern.
  • Research Potential: The compound has attracted interest in medicinal chemistry due to its structural motifs, which can inspire the design of new pharmaceuticals. Researchers are investigating how modifications to its structure can enhance its efficacy.

"Compounds like S-(4-nitrophenyl) N-methylcarbamothioate represent a fine balance between synthetic utility and biological significance."

This compound not only enriches our understanding of organosulfur compounds but also highlights the intricate link between molecular structure and biological activity, paving the way for future discoveries in chemistry and related fields.

Synonyms
22873-15-0
BRN 2114843
CARBAMIC ACID, METHYLTHIO-, S-(p-NITROPHENYL) ESTER
TL-1229
Carbamthiolic acid, N-methyl-, 4-nitrophenyl ester
DTXSID90177412
RefChem:332586
DTXCID9099903
SCHEMBL11326501