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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
(2-isopropoxyphenyl) N-methyl-N-(2-methylsulfanylacetyl)carbamate
State
State

At room temperature, carbaryl is a solid.

Melting point (Celsius)
142.50
Melting point (Kelvin)
415.65
Boiling point (Celsius)
274.80
Boiling point (Kelvin)
547.95
General information
Molecular weight
201.22g/mol
Molar mass
201.2190g/mol
Density
1.2300g/cm3
Appearence

Carbaryl is a white crystalline compound.

Comment on solubility

Solubility of (2-isopropoxyphenyl) N-methyl-N-(2-methylsulfanylacetyl)carbamate

The solubility of (2-isopropoxyphenyl) N-methyl-N-(2-methylsulfanylacetyl)carbamate can be influenced by various factors including temperature, polarity, and the presence of solvents. This compound features both hydrophobic and hydrophilic characteristics due to its alkyl and aromatic groups.

Key Points to Consider:

  • Polar vs. Non-Polar Solvents: The compound is likely to be more soluble in polar organic solvents, while its solubility in water is expected to be low due to the large non-polar phenyl group.
  • Temperature Effects: Increased temperature generally enhances solubility, allowing more significant dissolution of the compound in suitable solvents.
  • Functional Groups: The presence of the carbamate functional group can facilitate hydrogen bonding with polar solvents, slightly enhancing solubility under certain conditions.

In practice, solubility testing is essential to determine the specifics, as empirical data are valuable in establishing the exact behavior of this compound in various environments. Overall, understanding the solubility characteristics is crucial for applications in synthesis, formulation, and environmental studies.

Interesting facts

Interesting Facts about (2-isopropoxyphenyl) N-methyl-N-(2-methylsulfanylacetyl)carbamate

(2-isopropoxyphenyl) N-methyl-N-(2-methylsulfanylacetyl)carbamate, commonly referred to in the scientific community as a carbamate derivative, belongs to a class of compounds that have garnered significant attention in various fields. Here are some noteworthy points about this intriguing compound:

  • Biological Activity: Carbamates are known for their diverse biological properties, and this particular compound exhibits potential as a biological active agent. Its structure facilitates interactions with various biological targets, which may lead to applications in medicinal chemistry.
  • Synthetic Applications: The versatile nature of carbamates has led to extensive research around their synthesis. This compound can serve as a key intermediate in the preparation of other complex molecules, highlighting its importance in organic synthesis.
  • Environmental Significance: Carbamate compounds have implications in the study of pesticides and herbicides. Understanding their chemical behavior and stability in biological systems can offer insights into environmental impact and safety assessments.
  • Mechanism of Action: The unique structural arrangement of this compound suggests that it might interact with certain enzymes or receptors in the body. This raises intriguing questions about its mechanism of action and potential therapeutic benefits.
  • Research Frontier: As a relatively complex molecule, (2-isopropoxyphenyl) N-methyl-N-(2-methylsulfanylacetyl)carbamate presents opportunities for deeper exploration in fields such as pharmacology and toxicology, making it an exciting subject for future studies.

In conclusion, the exploration of (2-isopropoxyphenyl) N-methyl-N-(2-methylsulfanylacetyl)carbamate offers a fascinating glimpse into the world of carbamates, beckoning scientists and students alike to uncover its mysteries and harness its potential!

Synonyms
Upjohn U-22023
17959-12-5
CARBAMIC ACID, METHYL ((METHYLTHIO)ACETYL)-, o-ISOPROPOXYPHENYL ESTER
ENT 27,351
U-22023
NSC 190949
BRN 1890490
2-(1-Methylethoxy)phenyl methyl((methylthio)acetyl)carbamate
DTXSID80170836
DTXCID7093327
(2-propan-2-yloxyphenyl) N-methyl-N-(2-methylsulfanylacetyl)carbamate
T4UR4QE4LF
UNII-T4UR4QE4LF
(2-Propan-2-yloxyphenyl)n-methyl-N-(2-methylsulfanylacetyl)carbamate