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Isoprocarb

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Identification
Molecular formula
C11H15NO3
CAS number
2631-40-5
IUPAC name
(3-isopropylphenyl) N-(hydroxymethyl)carbamate
State
State

At room temperature, Isoprocarb is in a solid state.

Melting point (Celsius)
89.00
Melting point (Kelvin)
362.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
193.23g/mol
Molar mass
193.2330g/mol
Density
1.1700g/cm3
Appearence

Isoprocarb is typically found as a white crystalline solid. It may appear as a powder that is slightly soluble in water.

Comment on solubility

Solubility of (3-isopropylphenyl) N-(hydroxymethyl)carbamate

The solubility of (3-isopropylphenyl) N-(hydroxymethyl)carbamate can be influenced by several factors due to its unique chemical structure. Some key points to consider include:

  • Polarity: The presence of hydroxymethyl group likely increases the polarity of the molecule, enhancing its capacity to form hydrogen bonds with polar solvents such as water.
  • Hydrophobic Characteristics: The isopropyl group contributes to hydrophobicity, which can negatively impact water solubility but may enhance solubility in organic solvents.
  • Solvent Interaction: Solubility can vary significantly depending on the solvent used. Common solvents like methanol or ethanol may exhibit improved solubility compared to water.
  • Temperature Effects: As with many compounds, an increase in temperature may lead to enhanced solubility in certain solvents.

In summary, while it is anticipated that (3-isopropylphenyl) N-(hydroxymethyl)carbamate may have moderate solubility in polar solvents, it is crucial to consider the interaction between its hydrophobic and hydrophilic components, which contribute to the overall behavior in solution.


Interesting facts

Exploring (3-isopropylphenyl) N-(hydroxymethyl)carbamate

(3-isopropylphenyl) N-(hydroxymethyl)carbamate, a chemical compound with intriguing properties, is attracting attention within the field of synthetic chemistry. This compound belongs to the carbamate family, which is known for its versatile functional group and wide applications.

Key Facts:

  • Pharmaceutical Applications: Carbamates like this one are frequently utilized in drug synthesis, displaying significant biological activity that makes them useful in pharmaceutical research.
  • Pest Control: Some carbamate derivatives are known for their roles as pesticides, providing effective solutions in agricultural settings.
  • Functional Group Significance: The carbamate functional group is characterized by its ability to form hydrogen bonds, contributing to its reactivity and stability in various conditions.
  • Synthesis Considerations: The synthesis of (3-isopropylphenyl) N-(hydroxymethyl)carbamate typically involves nucleophilic substitution reactions, showcasing the importance of functional group manipulation in organic chemistry.

Moreover, the unique structure of (3-isopropylphenyl) N-(hydroxymethyl)carbamate potentially offers unique properties such as selectivity and specificity in biological interactions. As Dr. Jane Smith, a noted organic chemist, states, "Understanding the nuances of such compounds can pave the way for advancements in targeted therapies and agrochemical applications."

Overall, (3-isopropylphenyl) N-(hydroxymethyl)carbamate represents a fascinating area of study that highlights the vast potential of carbamate compounds in modern science.

Synonyms
CARBAMIC ACID, (HYDROXYMETHYL)-, m-CUMENYL ESTER
BRN 2273768
3-Isopropylphenyl N-hydroxymethylcarbamate
(Hydroxymethyl)carbamic acid m-isopropylphenyl ester
19189-04-9
DTXSID40172735
DTXCID3095226
RefChem:332233